Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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We've found
6,666
archived clinical trials in
Hospital

Evaluating Health Outcomes and QOL After ALI Among Participants of the ALTA, OMEGA, EDEN, and SAILS ARDS Network Trials
Patient Outcomes 6 and 12 Months After ALTA, OMEGA, EDEN and SAILS ARDS Network Trials
Status: Enrolling
Updated:  8/31/2015
University of Maryland Medical Center
mi
from
Baltimore, MD
Evaluating Health Outcomes and QOL After ALI Among Participants of the ALTA, OMEGA, EDEN, and SAILS ARDS Network Trials
Patient Outcomes 6 and 12 Months After ALTA, OMEGA, EDEN and SAILS ARDS Network Trials
Status: Enrolling
Updated: 8/31/2015
University of Maryland Medical Center
mi
from
Baltimore, MD
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Evaluating Health Outcomes and QOL After ALI Among Participants of the ALTA, OMEGA, EDEN, and SAILS ARDS Network Trials
Patient Outcomes 6 and 12 Months After ALTA, OMEGA, EDEN and SAILS ARDS Network Trials
Status: Enrolling
Updated:  8/31/2015
Wake Forest University
mi
from
Winston Salem, NC
Evaluating Health Outcomes and QOL After ALI Among Participants of the ALTA, OMEGA, EDEN, and SAILS ARDS Network Trials
Patient Outcomes 6 and 12 Months After ALTA, OMEGA, EDEN and SAILS ARDS Network Trials
Status: Enrolling
Updated: 8/31/2015
Wake Forest University
mi
from
Winston Salem, NC
Click here to add this to my saved trials
Evaluating Health Outcomes and QOL After ALI Among Participants of the ALTA, OMEGA, EDEN, and SAILS ARDS Network Trials
Patient Outcomes 6 and 12 Months After ALTA, OMEGA, EDEN and SAILS ARDS Network Trials
Status: Enrolling
Updated:  8/31/2015
Vanderbilt University
mi
from
Nashville, TN
Evaluating Health Outcomes and QOL After ALI Among Participants of the ALTA, OMEGA, EDEN, and SAILS ARDS Network Trials
Patient Outcomes 6 and 12 Months After ALTA, OMEGA, EDEN and SAILS ARDS Network Trials
Status: Enrolling
Updated: 8/31/2015
Vanderbilt University
mi
from
Nashville, TN
Click here to add this to my saved trials
Evaluating Health Outcomes and QOL After ALI Among Participants of the ALTA, OMEGA, EDEN, and SAILS ARDS Network Trials
Patient Outcomes 6 and 12 Months After ALTA, OMEGA, EDEN and SAILS ARDS Network Trials
Status: Enrolling
Updated:  8/31/2015
Intermountain Medical Center
mi
from
Murray, UT
Evaluating Health Outcomes and QOL After ALI Among Participants of the ALTA, OMEGA, EDEN, and SAILS ARDS Network Trials
Patient Outcomes 6 and 12 Months After ALTA, OMEGA, EDEN and SAILS ARDS Network Trials
Status: Enrolling
Updated: 8/31/2015
Intermountain Medical Center
mi
from
Murray, UT
Click here to add this to my saved trials
Evaluating Health Outcomes and QOL After ALI Among Participants of the ALTA, OMEGA, EDEN, and SAILS ARDS Network Trials
Patient Outcomes 6 and 12 Months After ALTA, OMEGA, EDEN and SAILS ARDS Network Trials
Status: Enrolling
Updated:  8/31/2015
University of Washington; Harborview Medical Center
mi
from
Seattle, WA
Evaluating Health Outcomes and QOL After ALI Among Participants of the ALTA, OMEGA, EDEN, and SAILS ARDS Network Trials
Patient Outcomes 6 and 12 Months After ALTA, OMEGA, EDEN and SAILS ARDS Network Trials
Status: Enrolling
Updated: 8/31/2015
University of Washington; Harborview Medical Center
mi
from
Seattle, WA
Click here to add this to my saved trials
Study of Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Impact of Daily Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Status: Enrolling
Updated:  9/1/2015
Childrens National Medical Center
mi
from
Washington,
Study of Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Impact of Daily Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Status: Enrolling
Updated: 9/1/2015
Childrens National Medical Center
mi
from
Washington,
Click here to add this to my saved trials
Study of Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Impact of Daily Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Status: Enrolling
Updated:  9/1/2015
Johns Hopkins Hospital
mi
from
Baltimore, MD
Study of Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Impact of Daily Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Status: Enrolling
Updated: 9/1/2015
Johns Hopkins Hospital
mi
from
Baltimore, MD
Click here to add this to my saved trials
Study of Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Impact of Daily Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Status: Enrolling
Updated:  9/1/2015
Saint Louis Children's Hospital
mi
from
Saint Louis, MO
Study of Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Impact of Daily Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Status: Enrolling
Updated: 9/1/2015
Saint Louis Children's Hospital
mi
from
Saint Louis, MO
Click here to add this to my saved trials
Study of Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Impact of Daily Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Status: Enrolling
Updated:  9/1/2015
Children's Hospital of Philadelphia
mi
from
Philadelphia, PA
Study of Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Impact of Daily Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Status: Enrolling
Updated: 9/1/2015
Children's Hospital of Philadelphia
mi
from
Philadelphia, PA
Click here to add this to my saved trials
Study of Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Impact of Daily Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Status: Enrolling
Updated:  9/1/2015
Seattle Children's Hospital
mi
from
Seattle, WA
Study of Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Impact of Daily Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Status: Enrolling
Updated: 9/1/2015
Seattle Children's Hospital
mi
from
Seattle, WA
Click here to add this to my saved trials
Statin Therapy in the Treatment of Sepsis
Study of Statin Therapy in the Treatment of Sepsis
Status: Enrolling
Updated:  9/3/2015
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Statin Therapy in the Treatment of Sepsis
Study of Statin Therapy in the Treatment of Sepsis
Status: Enrolling
Updated: 9/3/2015
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Click here to add this to my saved trials
Thiamine as a Metabolic Resuscitator in Septic Shock
Thiamine as a Metabolic Resuscitator in Septic Shock
Status: Enrolling
Updated:  9/3/2015
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Thiamine as a Metabolic Resuscitator in Septic Shock
Thiamine as a Metabolic Resuscitator in Septic Shock
Status: Enrolling
Updated: 9/3/2015
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Click here to add this to my saved trials
How Lidocaine Affects Outcomes In Orthopedic Surgery Patients
The Effects Of Lidocaine Infusion On The Recovery Of Cognitive Function Following General Anesthesia In Elderly Patients Undergoing Orthopedic Surgeries Requiring A Minimum Two Day Hospitalization
Status: Enrolling
Updated:  9/3/2015
Cedars-Sinai Medical Center
mi
from
Los Angeles, CA
How Lidocaine Affects Outcomes In Orthopedic Surgery Patients
The Effects Of Lidocaine Infusion On The Recovery Of Cognitive Function Following General Anesthesia In Elderly Patients Undergoing Orthopedic Surgeries Requiring A Minimum Two Day Hospitalization
Status: Enrolling
Updated: 9/3/2015
Cedars-Sinai Medical Center
mi
from
Los Angeles, CA
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Ubiquinol (Reduced COQ10) for Patients With Sepsis
Ubiquinol (Reduced COQ10) for Patients With Sepsis
Status: Enrolling
Updated:  9/3/2015
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Ubiquinol (Reduced COQ10) for Patients With Sepsis
Ubiquinol (Reduced COQ10) for Patients With Sepsis
Status: Enrolling
Updated: 9/3/2015
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Click here to add this to my saved trials
Clipping Versus No Hair Removal and the Risk of Surgical Site Infections
Clipping vs. No Hair Removal and the Risk of Surgical Site Infection: A Randomized, Assessor Blinded Non-inferiority Clinical Trial Among Patients Undergoing General Surgical Procedures at a Community Hospital
Status: Enrolling
Updated:  9/4/2015
Gundersen Lutheran Health System
mi
from
La Crosse, WI
Clipping Versus No Hair Removal and the Risk of Surgical Site Infections
Clipping vs. No Hair Removal and the Risk of Surgical Site Infection: A Randomized, Assessor Blinded Non-inferiority Clinical Trial Among Patients Undergoing General Surgical Procedures at a Community Hospital
Status: Enrolling
Updated: 9/4/2015
Gundersen Lutheran Health System
mi
from
La Crosse, WI
Click here to add this to my saved trials
Clipped Versus Handsewn Arteriovenous Fistula Anastomosis
The Safety and Effectiveness of Clipped Technique vs. Hand-Sewn Technique for Anastomosis in Arteriovenous Fistulas
Status: Enrolling
Updated:  9/4/2015
Gundersen Lutheran Health System
mi
from
La Crosse, WI
Clipped Versus Handsewn Arteriovenous Fistula Anastomosis
The Safety and Effectiveness of Clipped Technique vs. Hand-Sewn Technique for Anastomosis in Arteriovenous Fistulas
Status: Enrolling
Updated: 9/4/2015
Gundersen Lutheran Health System
mi
from
La Crosse, WI
Click here to add this to my saved trials
Open-Label, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gestational Age
A Phase II/III, Open-Label, Multicenter, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gestational Age
Status: Enrolling
Updated:  9/8/2015
Clinical Research Facility
mi
from
Louisville, KY
Open-Label, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gestational Age
A Phase II/III, Open-Label, Multicenter, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gestational Age
Status: Enrolling
Updated: 9/8/2015
Clinical Research Facility
mi
from
Louisville, KY
Click here to add this to my saved trials
Open-Label, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gestational Age
A Phase II/III, Open-Label, Multicenter, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gestational Age
Status: Enrolling
Updated:  9/8/2015
Clinical Research Facility
mi
from
Pittsburgh, PA
Open-Label, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gestational Age
A Phase II/III, Open-Label, Multicenter, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gestational Age
Status: Enrolling
Updated: 9/8/2015
Clinical Research Facility
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
Open-Label, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gestational Age
A Phase II/III, Open-Label, Multicenter, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gestational Age
Status: Enrolling
Updated:  9/8/2015
Clinical Research Facility
mi
from
Greenville, SC
Open-Label, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gestational Age
A Phase II/III, Open-Label, Multicenter, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gestational Age
Status: Enrolling
Updated: 9/8/2015
Clinical Research Facility
mi
from
Greenville, SC
Click here to add this to my saved trials
Open-Label, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gestational Age
A Phase II/III, Open-Label, Multicenter, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gestational Age
Status: Enrolling
Updated:  9/8/2015
Clinical Research Facility
mi
from
Morgantown, WV
Open-Label, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gestational Age
A Phase II/III, Open-Label, Multicenter, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gestational Age
Status: Enrolling
Updated: 9/8/2015
Clinical Research Facility
mi
from
Morgantown, WV
Click here to add this to my saved trials
Serotonergic Modulation of Motor Function in Subacute and Chronic SCI
Serotonergic Modulation of Motor Function in Subacute and Chronic SCI
Status: Enrolling
Updated:  9/8/2015
Rehabilitation Institute of Chicago
mi
from
Chicago, IL
Serotonergic Modulation of Motor Function in Subacute and Chronic SCI
Serotonergic Modulation of Motor Function in Subacute and Chronic SCI
Status: Enrolling
Updated: 9/8/2015
Rehabilitation Institute of Chicago
mi
from
Chicago, IL
Click here to add this to my saved trials
Safety, Tolerability, and Immunogenicity of the Human Cytomegalovirus Vaccine (V160) in Healthy Adults (V160-001)
A Phase 1 Randomized, Double-Blind, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety, Tolerability, and Immunogenicity of the Human Cytomegalovirus Vaccine (V160) in Healthy Adults
Status: Enrolling
Updated:  9/8/2015
Clinical Research Facility
mi
from
Chicago, IL
Safety, Tolerability, and Immunogenicity of the Human Cytomegalovirus Vaccine (V160) in Healthy Adults (V160-001)
A Phase 1 Randomized, Double-Blind, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety, Tolerability, and Immunogenicity of the Human Cytomegalovirus Vaccine (V160) in Healthy Adults
Status: Enrolling
Updated: 9/8/2015
Clinical Research Facility
mi
from
Chicago, IL
Click here to add this to my saved trials
Safety, Tolerability, and Immunogenicity of the Human Cytomegalovirus Vaccine (V160) in Healthy Adults (V160-001)
A Phase 1 Randomized, Double-Blind, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety, Tolerability, and Immunogenicity of the Human Cytomegalovirus Vaccine (V160) in Healthy Adults
Status: Enrolling
Updated:  9/8/2015
Clinical Research Facility
mi
from
Baltimore, MD
Safety, Tolerability, and Immunogenicity of the Human Cytomegalovirus Vaccine (V160) in Healthy Adults (V160-001)
A Phase 1 Randomized, Double-Blind, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety, Tolerability, and Immunogenicity of the Human Cytomegalovirus Vaccine (V160) in Healthy Adults
Status: Enrolling
Updated: 9/8/2015
Clinical Research Facility
mi
from
Baltimore, MD
Click here to add this to my saved trials
Safety, Tolerability, and Immunogenicity of the Human Cytomegalovirus Vaccine (V160) in Healthy Adults (V160-001)
A Phase 1 Randomized, Double-Blind, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety, Tolerability, and Immunogenicity of the Human Cytomegalovirus Vaccine (V160) in Healthy Adults
Status: Enrolling
Updated:  9/8/2015
Clinical Research Facility
mi
from
Richmond, VA
Safety, Tolerability, and Immunogenicity of the Human Cytomegalovirus Vaccine (V160) in Healthy Adults (V160-001)
A Phase 1 Randomized, Double-Blind, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety, Tolerability, and Immunogenicity of the Human Cytomegalovirus Vaccine (V160) in Healthy Adults
Status: Enrolling
Updated: 9/8/2015
Clinical Research Facility
mi
from
Richmond, VA
Click here to add this to my saved trials
BEST (Burn Center Evaluation of Standard Therapies) Ventilator Mode Study-
BEST (Burn Center Evaluation of Standard Therapies) Ventilator Mode Study: A Prospective Randomized Controlled Trial
Status: Enrolling
Updated:  9/8/2015
United States Army Institute of Surgical Research
mi
from
Fort Sam Houston, TX
BEST (Burn Center Evaluation of Standard Therapies) Ventilator Mode Study-
BEST (Burn Center Evaluation of Standard Therapies) Ventilator Mode Study: A Prospective Randomized Controlled Trial
Status: Enrolling
Updated: 9/8/2015
United States Army Institute of Surgical Research
mi
from
Fort Sam Houston, TX
Click here to add this to my saved trials
Effects of Intravenous Acetaminophen on Body Temperature and Hemodynamic Responses in Febrile Critically Ill Adults
Effects of Intravenous Acetaminophen on Body Temperature and Hemodynamic Responses in Febrile Critically Ill Adults: a Randomized Controlled Trial
Status: Enrolling
Updated:  9/10/2015
UCSF Medical Center
mi
from
San Francisco, CA
Effects of Intravenous Acetaminophen on Body Temperature and Hemodynamic Responses in Febrile Critically Ill Adults
Effects of Intravenous Acetaminophen on Body Temperature and Hemodynamic Responses in Febrile Critically Ill Adults: a Randomized Controlled Trial
Status: Enrolling
Updated: 9/10/2015
UCSF Medical Center
mi
from
San Francisco, CA
Click here to add this to my saved trials
Effects of Intravenous Acetaminophen on Body Temperature and Hemodynamic Responses in Febrile Critically Ill Adults
Effects of Intravenous Acetaminophen on Body Temperature and Hemodynamic Responses in Febrile Critically Ill Adults: a Randomized Controlled Trial
Status: Enrolling
Updated:  9/10/2015
University of California, San Francisco Medical Center
mi
from
San Francisco, CA
Effects of Intravenous Acetaminophen on Body Temperature and Hemodynamic Responses in Febrile Critically Ill Adults
Effects of Intravenous Acetaminophen on Body Temperature and Hemodynamic Responses in Febrile Critically Ill Adults: a Randomized Controlled Trial
Status: Enrolling
Updated: 9/10/2015
University of California, San Francisco Medical Center
mi
from
San Francisco, CA
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Enhancement of Pressure Healing With Pulsatile Lavage
Enhancement of Pressure Healing With Pulsatile Lavage
Status: Enrolling
Updated:  9/10/2015
VA Medical Center, Cleveland
mi
from
Cleveland, OH
Enhancement of Pressure Healing With Pulsatile Lavage
Enhancement of Pressure Healing With Pulsatile Lavage
Status: Enrolling
Updated: 9/10/2015
VA Medical Center, Cleveland
mi
from
Cleveland, OH
Click here to add this to my saved trials
Botox-A Injection to Improve Bladder Function in Early Spinal Cord Injury (#H-20344)
Botulinum Toxin A Treatment of Detrusor External Sphincter Dyssynergia During Early Spinal Cord Injury (Protocol #H-20344)
Status: Enrolling
Updated:  9/11/2015
Baylor College of Medicine
mi
from
Houston, TX
Botox-A Injection to Improve Bladder Function in Early Spinal Cord Injury (#H-20344)
Botulinum Toxin A Treatment of Detrusor External Sphincter Dyssynergia During Early Spinal Cord Injury (Protocol #H-20344)
Status: Enrolling
Updated: 9/11/2015
Baylor College of Medicine
mi
from
Houston, TX
Click here to add this to my saved trials
Botox-A Injection to Improve Bladder Function in Early Spinal Cord Injury (#H-20344)
Botulinum Toxin A Treatment of Detrusor External Sphincter Dyssynergia During Early Spinal Cord Injury (Protocol #H-20344)
Status: Enrolling
Updated:  9/11/2015
Memorial Hermann Hospital/The Institute of Rehabilitation and Research
mi
from
Houston, TX
Botox-A Injection to Improve Bladder Function in Early Spinal Cord Injury (#H-20344)
Botulinum Toxin A Treatment of Detrusor External Sphincter Dyssynergia During Early Spinal Cord Injury (Protocol #H-20344)
Status: Enrolling
Updated: 9/11/2015
Memorial Hermann Hospital/The Institute of Rehabilitation and Research
mi
from
Houston, TX
Click here to add this to my saved trials
Dexmedetomidine Versus Propofol for Prolonged Sedation in Critically Ill Trauma and Surgical Patients
Dexmedetomidine Versus Propofol for Prolonged Sedation in Critically Ill Trauma and Surgical Patients
Status: Enrolling
Updated:  9/11/2015
University of Tennessee Medical Center
mi
from
Knoxville, TN
Dexmedetomidine Versus Propofol for Prolonged Sedation in Critically Ill Trauma and Surgical Patients
Dexmedetomidine Versus Propofol for Prolonged Sedation in Critically Ill Trauma and Surgical Patients
Status: Enrolling
Updated: 9/11/2015
University of Tennessee Medical Center
mi
from
Knoxville, TN
Click here to add this to my saved trials
Paclitaxel for the Treatment of Upper-Extremity Arteriovenous Access Fistula Stenosis
The Use of Intravascular Paclitaxel for the Treatment of Upper-Extremity Arteriovenous Access Fistula Stenosis: A Randomized Study
Status: Enrolling
Updated:  9/14/2015
Englewood Hospital and Medical Center
mi
from
Englewood, NJ
Paclitaxel for the Treatment of Upper-Extremity Arteriovenous Access Fistula Stenosis
The Use of Intravascular Paclitaxel for the Treatment of Upper-Extremity Arteriovenous Access Fistula Stenosis: A Randomized Study
Status: Enrolling
Updated: 9/14/2015
Englewood Hospital and Medical Center
mi
from
Englewood, NJ
Click here to add this to my saved trials
Infant Pulmonary Mechanics: High Flow Nasal Cannula Versus Nasal CPAP
Pulmonary Mechanics in Preterm Infants Treated With Heated Humidified High Flow Nasal Cannula as Compared to Nasal Continuous Positive Airway Pressure.
Status: Enrolling
Updated:  9/14/2015
Pennsylvania Hospital
mi
from
Philadelphia, PA
Infant Pulmonary Mechanics: High Flow Nasal Cannula Versus Nasal CPAP
Pulmonary Mechanics in Preterm Infants Treated With Heated Humidified High Flow Nasal Cannula as Compared to Nasal Continuous Positive Airway Pressure.
Status: Enrolling
Updated: 9/14/2015
Pennsylvania Hospital
mi
from
Philadelphia, PA
Click here to add this to my saved trials
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated:  9/16/2015
Shoals Medical Trials, Inc
mi
from
Sheffield, AL
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated: 9/16/2015
Shoals Medical Trials, Inc
mi
from
Sheffield, AL
Click here to add this to my saved trials
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated:  9/16/2015
Florida Research Associates, LLC
mi
from
Deland, FL
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated: 9/16/2015
Florida Research Associates, LLC
mi
from
Deland, FL
Click here to add this to my saved trials
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated:  9/16/2015
Pensacola Research Consultants, Inc.
mi
from
Pensacola, FL
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated: 9/16/2015
Pensacola Research Consultants, Inc.
mi
from
Pensacola, FL
Click here to add this to my saved trials
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated:  9/16/2015
Ohio State University
mi
from
Columbus, OH
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated: 9/16/2015
Ohio State University
mi
from
Columbus, OH
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A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated:  9/16/2015
Endeavor Clinical Trials, PA
mi
from
San Antonio, TX
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated: 9/16/2015
Endeavor Clinical Trials, PA
mi
from
San Antonio, TX
Click here to add this to my saved trials
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated:  9/16/2015
Eliza Coffee Memorial Hospital
mi
from
Florence, AL
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated: 9/16/2015
Eliza Coffee Memorial Hospital
mi
from
Florence, AL
Click here to add this to my saved trials
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated:  9/16/2015
Drug Research Analysis Corp
mi
from
Montgomery, AL
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated: 9/16/2015
Drug Research Analysis Corp
mi
from
Montgomery, AL
Click here to add this to my saved trials
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated:  9/16/2015
Arizona Research Center
mi
from
Phoenix, AZ
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated: 9/16/2015
Arizona Research Center
mi
from
Phoenix, AZ
Click here to add this to my saved trials
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated:  9/16/2015
Thorton Hospital
mi
from
San Diego, CA
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated: 9/16/2015
Thorton Hospital
mi
from
San Diego, CA
Click here to add this to my saved trials
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated:  9/16/2015
River City Clinical Research
mi
from
Jacksonville, FL
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated: 9/16/2015
River City Clinical Research
mi
from
Jacksonville, FL
Click here to add this to my saved trials
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated:  9/16/2015
Gulfcoast Research Institute, LLC
mi
from
Sarasota, FL
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated: 9/16/2015
Gulfcoast Research Institute, LLC
mi
from
Sarasota, FL
Click here to add this to my saved trials
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated:  9/16/2015
Phoenix Clinical Research
mi
from
Tamarac, FL
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated: 9/16/2015
Phoenix Clinical Research
mi
from
Tamarac, FL
Click here to add this to my saved trials
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated:  9/16/2015
Cleveland Clinic Foundation
mi
from
Cleveland, OH
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated: 9/16/2015
Cleveland Clinic Foundation
mi
from
Cleveland, OH
Click here to add this to my saved trials
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated:  9/16/2015
Access Clinical Trials
mi
from
Nashville, TN
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated: 9/16/2015
Access Clinical Trials
mi
from
Nashville, TN
Click here to add this to my saved trials
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated:  9/16/2015
Jean Brown Research
mi
from
Salt Lake City, UT
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™) to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain
Status: Enrolling
Updated: 9/16/2015
Jean Brown Research
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Hypoxia Inducible Factor 1 Alpha as a Novel Biomarker in Septic Shock
Hypoxia Inducible Factor 1 Alpha as a Novel Biomarker in Septic Shock
Status: Enrolling
Updated:  9/17/2015
University of Florida
mi
from
Gainesville, FL
Hypoxia Inducible Factor 1 Alpha as a Novel Biomarker in Septic Shock
Hypoxia Inducible Factor 1 Alpha as a Novel Biomarker in Septic Shock
Status: Enrolling
Updated: 9/17/2015
University of Florida
mi
from
Gainesville, FL
Click here to add this to my saved trials
Efficacy Study on Silver-coated ETT Cleaned With a Novel Device
Silver-coated Endotracheal Tube Cleaned With a Novel Mechanism for Secretion Removal: a Randomized Controlled Clinical Study.
Status: Enrolling
Updated:  9/22/2015
Massachusetts General Hospital
mi
from
Boston, MA
Efficacy Study on Silver-coated ETT Cleaned With a Novel Device
Silver-coated Endotracheal Tube Cleaned With a Novel Mechanism for Secretion Removal: a Randomized Controlled Clinical Study.
Status: Enrolling
Updated: 9/22/2015
Massachusetts General Hospital
mi
from
Boston, MA
Click here to add this to my saved trials