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

Translational Approaches to Septic Cardiomyopathy
Translational Approaches to Septic Cardiomyopathy
Status: Enrolling
Updated:  12/31/1969
Intermoutain Medical Center
mi
from
Murray, UT
Translational Approaches to Septic Cardiomyopathy
Translational Approaches to Septic Cardiomyopathy
Status: Enrolling
Updated: 12/31/1969
Intermoutain Medical Center
mi
from
Murray, UT
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Evaluating Quality of Life for Patients With Chronic Obstructive Pulmonary Disease Who Are Undergoing Lung Transplantation
Lung Transplant for COPD: Outcomes/Technology
Status: Enrolling
Updated:  12/31/1969
Washington University School of Medicine @ Barnes-Jewish Hospital
mi
from
Saint Louis, MO
Evaluating Quality of Life for Patients With Chronic Obstructive Pulmonary Disease Who Are Undergoing Lung Transplantation
Lung Transplant for COPD: Outcomes/Technology
Status: Enrolling
Updated: 12/31/1969
Washington University School of Medicine @ Barnes-Jewish Hospital
mi
from
Saint Louis, MO
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StrataGraft™ Skin Tissue (Human Donor Skin) In The Surgical Management Of Complex Skin Defects
Open-Label, Controlled, Randomized, Comparative, Dose Escalation Study Of The Safety, Human Immunology, And Efficacy Of StrataGraft™ Skin Tissue (Human Donor Skin) In The Surgical Management Of Complex Skin Defects In Patients Undergoing Sequential Skin Reconstruction Procedures
Status: Enrolling
Updated:  12/31/1969
Arizona Burn & Trauma Center
mi
from
Phoenix, AZ
StrataGraft™ Skin Tissue (Human Donor Skin) In The Surgical Management Of Complex Skin Defects
Open-Label, Controlled, Randomized, Comparative, Dose Escalation Study Of The Safety, Human Immunology, And Efficacy Of StrataGraft™ Skin Tissue (Human Donor Skin) In The Surgical Management Of Complex Skin Defects In Patients Undergoing Sequential Skin Reconstruction Procedures
Status: Enrolling
Updated: 12/31/1969
Arizona Burn & Trauma Center
mi
from
Phoenix, AZ
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StrataGraft™ Skin Tissue (Human Donor Skin) In The Surgical Management Of Complex Skin Defects
Open-Label, Controlled, Randomized, Comparative, Dose Escalation Study Of The Safety, Human Immunology, And Efficacy Of StrataGraft™ Skin Tissue (Human Donor Skin) In The Surgical Management Of Complex Skin Defects In Patients Undergoing Sequential Skin Reconstruction Procedures
Status: Enrolling
Updated:  12/31/1969
University of Wisconsin Hospital and Clinics
mi
from
Madison, WI
StrataGraft™ Skin Tissue (Human Donor Skin) In The Surgical Management Of Complex Skin Defects
Open-Label, Controlled, Randomized, Comparative, Dose Escalation Study Of The Safety, Human Immunology, And Efficacy Of StrataGraft™ Skin Tissue (Human Donor Skin) In The Surgical Management Of Complex Skin Defects In Patients Undergoing Sequential Skin Reconstruction Procedures
Status: Enrolling
Updated: 12/31/1969
University of Wisconsin Hospital and Clinics
mi
from
Madison, WI
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Guanfacine for PONV and Pain After Sinus Surgery
Guanfacine for PONV and Pain After Sinus Surgery
Status: Enrolling
Updated:  12/31/1969
Vanderbilt University Medical Center
mi
from
Nashville, TN
Guanfacine for PONV and Pain After Sinus Surgery
Guanfacine for PONV and Pain After Sinus Surgery
Status: Enrolling
Updated: 12/31/1969
Vanderbilt University Medical Center
mi
from
Nashville, TN
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Use of the SNAP II Electroencephalography (EEG) Monitor in Outpatients Undergoing Surgery/Procedures With Sedation
Use of the SNAP II EEG Monitor in Outpatients Undergoing Surgery/Procedures With Sedation
Status: Enrolling
Updated:  12/31/1969
University of Wisconsin Hospital and Clinics
mi
from
Madison, WI
Use of the SNAP II Electroencephalography (EEG) Monitor in Outpatients Undergoing Surgery/Procedures With Sedation
Use of the SNAP II EEG Monitor in Outpatients Undergoing Surgery/Procedures With Sedation
Status: Enrolling
Updated: 12/31/1969
University of Wisconsin Hospital and Clinics
mi
from
Madison, WI
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Impact of Intraoperative Fluid Management on Electrolyte and Acid-base Variables
Impact of Intraoperative Fluid Management on Electrolyte and Acid-base Variables
Status: Enrolling
Updated:  12/31/1969
Nationwide Children's Hospital
mi
from
Columbus, OH
Impact of Intraoperative Fluid Management on Electrolyte and Acid-base Variables
Impact of Intraoperative Fluid Management on Electrolyte and Acid-base Variables
Status: Enrolling
Updated: 12/31/1969
Nationwide Children's Hospital
mi
from
Columbus, OH
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Antibiotic Administration and Blood Culture Positivity in Severe Sepsis and Septic Shock
The Effect of Antibiotic Administration on Blood Culture Positivity in Patients With Severe Sepsis and Septic Shock: a Prospective Multicenter Observational Trial.
Status: Enrolling
Updated:  12/31/1969
Maricopa Integrated Health Center
mi
from
Phoenix, AZ
Antibiotic Administration and Blood Culture Positivity in Severe Sepsis and Septic Shock
The Effect of Antibiotic Administration on Blood Culture Positivity in Patients With Severe Sepsis and Septic Shock: a Prospective Multicenter Observational Trial.
Status: Enrolling
Updated: 12/31/1969
Maricopa Integrated Health Center
mi
from
Phoenix, AZ
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Antibiotic Administration and Blood Culture Positivity in Severe Sepsis and Septic Shock
The Effect of Antibiotic Administration on Blood Culture Positivity in Patients With Severe Sepsis and Septic Shock: a Prospective Multicenter Observational Trial.
Status: Enrolling
Updated:  12/31/1969
Lions Gate Hospital
mi
from
North Vancouver,
Antibiotic Administration and Blood Culture Positivity in Severe Sepsis and Septic Shock
The Effect of Antibiotic Administration on Blood Culture Positivity in Patients With Severe Sepsis and Septic Shock: a Prospective Multicenter Observational Trial.
Status: Enrolling
Updated: 12/31/1969
Lions Gate Hospital
mi
from
North Vancouver,
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Vasopressin Plasma Concentrations in Patients Receiving Exogenous Vasopressin Infusion for Septic Shock
Vasopressin Plasma Concentrations in Responders and Non-responders to Exogenous Vasopressin Infusion in Patients With Septic Shock
Status: Enrolling
Updated:  12/31/1969
Cleveland Clinic
mi
from
Cleveland, OH
Vasopressin Plasma Concentrations in Patients Receiving Exogenous Vasopressin Infusion for Septic Shock
Vasopressin Plasma Concentrations in Responders and Non-responders to Exogenous Vasopressin Infusion in Patients With Septic Shock
Status: Enrolling
Updated: 12/31/1969
Cleveland Clinic
mi
from
Cleveland, OH
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Programming Implantable Cardioverter Defibrillators in Patients With Primary Prevention Indication
Programming Implantable Cardioverter Defibrillators (ICDs) in Patients With Primary Prevention Indication to Prolong Time to First Shock
Status: Enrolling
Updated:  12/31/1969
Hall-Garcia Cardiology Associates
mi
from
Houston, TX
Programming Implantable Cardioverter Defibrillators in Patients With Primary Prevention Indication
Programming Implantable Cardioverter Defibrillators (ICDs) in Patients With Primary Prevention Indication to Prolong Time to First Shock
Status: Enrolling
Updated: 12/31/1969
Hall-Garcia Cardiology Associates
mi
from
Houston, TX
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Feasibility of a Standardized Video for Patient Education and as a Decision Aid on Code Status for Patients in the Emergency Department Pending Admission to the Hospital
Feasibility of a Standardized Video for Patient Education and as a Decision Aid on Code Status for Patients in the Emergency Department Pending Admission to the Hospital
Status: Enrolling
Updated:  12/31/1969
Mayo Clinic Rochester
mi
from
Rochester, MN
Feasibility of a Standardized Video for Patient Education and as a Decision Aid on Code Status for Patients in the Emergency Department Pending Admission to the Hospital
Feasibility of a Standardized Video for Patient Education and as a Decision Aid on Code Status for Patients in the Emergency Department Pending Admission to the Hospital
Status: Enrolling
Updated: 12/31/1969
Mayo Clinic Rochester
mi
from
Rochester, MN
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Red Blood Cell Transfusion in the Ambulatory Setting: Impact on Home Functional Status
Red Blood Cell Transfusion in the Ambulatory Setting: Impact on Home Functional Status
Status: Enrolling
Updated:  12/31/1969
Mayo Clinic Arizona
mi
from
Scottsdale, AZ
Red Blood Cell Transfusion in the Ambulatory Setting: Impact on Home Functional Status
Red Blood Cell Transfusion in the Ambulatory Setting: Impact on Home Functional Status
Status: Enrolling
Updated: 12/31/1969
Mayo Clinic Arizona
mi
from
Scottsdale, AZ
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End-tidal Oxygen Can Reliably Predict the Arterial Partial Pressure of Oxygen Among Emergency Department Patients
End-tidal Oxygen Can Reliably Predict the Arterial Partial Pressure of Oxygen Among Emergency Department Patients Undergoing Rapid Sequence Intubation
Status: Enrolling
Updated:  12/31/1969
NYC H+H/Lincoln
mi
from
Bronx, NY
End-tidal Oxygen Can Reliably Predict the Arterial Partial Pressure of Oxygen Among Emergency Department Patients
End-tidal Oxygen Can Reliably Predict the Arterial Partial Pressure of Oxygen Among Emergency Department Patients Undergoing Rapid Sequence Intubation
Status: Enrolling
Updated: 12/31/1969
NYC H+H/Lincoln
mi
from
Bronx, NY
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Comparison of a Novel Wound Dressing Stratamed Versus Current Clinical Practice After Follicular Unit Extraction Hair Transplantation
Comparison of a Novel Wound Dressing Stratamed Versus Current Clinical Practice After Follicular Unit Extraction Hair Transplantation
Status: Enrolling
Updated:  12/31/1969
New Jersey Plastic Surgery, Montclair, NJ USA
mi
from
Montclair, NJ
Comparison of a Novel Wound Dressing Stratamed Versus Current Clinical Practice After Follicular Unit Extraction Hair Transplantation
Comparison of a Novel Wound Dressing Stratamed Versus Current Clinical Practice After Follicular Unit Extraction Hair Transplantation
Status: Enrolling
Updated: 12/31/1969
New Jersey Plastic Surgery, Montclair, NJ USA
mi
from
Montclair, NJ
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Neurodegeneration in Newborns After Anesthetics
Measurement of Biomarkers of Neurodegeneration in Newborns After Exposure to Anesthetics
Status: Enrolling
Updated:  12/31/1969
Univ of Pennsylvania
mi
from
Philadelphia, PA
Neurodegeneration in Newborns After Anesthetics
Measurement of Biomarkers of Neurodegeneration in Newborns After Exposure to Anesthetics
Status: Enrolling
Updated: 12/31/1969
Univ of Pennsylvania
mi
from
Philadelphia, PA
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Acute Effect of Ventilatory Support During Exercise in Spinal Cord Injury
Acute Effect of Ventilatory Support During Exercise in Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
Spaulding Hospital Cambridge
mi
from
Cambridge, MA
Acute Effect of Ventilatory Support During Exercise in Spinal Cord Injury
Acute Effect of Ventilatory Support During Exercise in Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Spaulding Hospital Cambridge
mi
from
Cambridge, MA
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Deployment Related Mild Traumatic Brain Injury (mTBI)
Deployment Related Mild Traumatic Brain Injury (mTBI): Incidence, Natural History, and Predictors of Recovery in Soldiers Returning From OIF/OEF
Status: Enrolling
Updated:  12/31/1969
Fort Carson
mi
from
Fort Carson, CO
Deployment Related Mild Traumatic Brain Injury (mTBI)
Deployment Related Mild Traumatic Brain Injury (mTBI): Incidence, Natural History, and Predictors of Recovery in Soldiers Returning From OIF/OEF
Status: Enrolling
Updated: 12/31/1969
Fort Carson
mi
from
Fort Carson, CO
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Deployment Related Mild Traumatic Brain Injury (mTBI)
Deployment Related Mild Traumatic Brain Injury (mTBI): Incidence, Natural History, and Predictors of Recovery in Soldiers Returning From OIF/OEF
Status: Enrolling
Updated:  12/31/1969
Fort Bragg
mi
from
Fort Bragg, NC
Deployment Related Mild Traumatic Brain Injury (mTBI)
Deployment Related Mild Traumatic Brain Injury (mTBI): Incidence, Natural History, and Predictors of Recovery in Soldiers Returning From OIF/OEF
Status: Enrolling
Updated: 12/31/1969
Fort Bragg
mi
from
Fort Bragg, NC
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Phase II Dose-ranging Study of APD421 in PONV
Randomised, Double-blind, Placebo-controlled, Dose-ranging Phase II Study of APD421 for the Prevention of Post-operative Nausea and Vomiting
Status: Enrolling
Updated:  12/31/1969
Duke Univ Med Ctr
mi
from
Durham, NC
Phase II Dose-ranging Study of APD421 in PONV
Randomised, Double-blind, Placebo-controlled, Dose-ranging Phase II Study of APD421 for the Prevention of Post-operative Nausea and Vomiting
Status: Enrolling
Updated: 12/31/1969
Duke Univ Med Ctr
mi
from
Durham, NC
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Phase II Dose-ranging Study of APD421 in PONV
Randomised, Double-blind, Placebo-controlled, Dose-ranging Phase II Study of APD421 for the Prevention of Post-operative Nausea and Vomiting
Status: Enrolling
Updated:  12/31/1969
University Hospital
mi
from
Besançon,
Phase II Dose-ranging Study of APD421 in PONV
Randomised, Double-blind, Placebo-controlled, Dose-ranging Phase II Study of APD421 for the Prevention of Post-operative Nausea and Vomiting
Status: Enrolling
Updated: 12/31/1969
University Hospital
mi
from
Besançon,
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Aspirin and Enoxaparin for VTE in Trauma
The Role Of Combined Therapy With Aspirin and Enoxaparin In Prevention Of Venous Thromboembolism In Trauma Patients: A Randomized-Controlled Trial
Status: Enrolling
Updated:  12/31/1969
Ryder Trauma Center
mi
from
Miami, FL
Aspirin and Enoxaparin for VTE in Trauma
The Role Of Combined Therapy With Aspirin and Enoxaparin In Prevention Of Venous Thromboembolism In Trauma Patients: A Randomized-Controlled Trial
Status: Enrolling
Updated: 12/31/1969
Ryder Trauma Center
mi
from
Miami, FL
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Evaluate the Analgesic Efficacy and Safety of VVZ-149 Injections for Post-Operative Pain Following Laparoscopic Colorectomy
A Randomized, Double-Blind, Parallel Group, Placebo-Controlled Dose Finding Study to Evaluate the Analgesic Efficacy and Safety of VVZ-149 Injections for Post-Operative Pain Following Laparoscopic Colorectal Surgery
Status: Enrolling
Updated:  12/31/1969
Massachusetts General Hospital
mi
from
Boston, MA
Evaluate the Analgesic Efficacy and Safety of VVZ-149 Injections for Post-Operative Pain Following Laparoscopic Colorectomy
A Randomized, Double-Blind, Parallel Group, Placebo-Controlled Dose Finding Study to Evaluate the Analgesic Efficacy and Safety of VVZ-149 Injections for Post-Operative Pain Following Laparoscopic Colorectal Surgery
Status: Enrolling
Updated: 12/31/1969
Massachusetts General Hospital
mi
from
Boston, MA
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Evaluate the Analgesic Efficacy and Safety of VVZ-149 Injections for Post-Operative Pain Following Laparoscopic Colorectomy
A Randomized, Double-Blind, Parallel Group, Placebo-Controlled Dose Finding Study to Evaluate the Analgesic Efficacy and Safety of VVZ-149 Injections for Post-Operative Pain Following Laparoscopic Colorectal Surgery
Status: Enrolling
Updated:  12/31/1969
Brigham and Women's Hosp
mi
from
Boston, MA
Evaluate the Analgesic Efficacy and Safety of VVZ-149 Injections for Post-Operative Pain Following Laparoscopic Colorectomy
A Randomized, Double-Blind, Parallel Group, Placebo-Controlled Dose Finding Study to Evaluate the Analgesic Efficacy and Safety of VVZ-149 Injections for Post-Operative Pain Following Laparoscopic Colorectal Surgery
Status: Enrolling
Updated: 12/31/1969
Brigham and Women's Hosp
mi
from
Boston, MA
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Thiamine Supplementation in Patients With Septic Shock
Thiamine Supplementation in Patients With Septic Shock: A Randomized, Double Blind, Placebo Controlled Trial
Status: Enrolling
Updated:  12/31/1969
Cleveland Clinic Florida
mi
from
Weston, FL
Thiamine Supplementation in Patients With Septic Shock
Thiamine Supplementation in Patients With Septic Shock: A Randomized, Double Blind, Placebo Controlled Trial
Status: Enrolling
Updated: 12/31/1969
Cleveland Clinic Florida
mi
from
Weston, FL
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Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection
Randomized Clinical Trial of Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection in Very-Low-Birth-Weight Infants
Status: Enrolling
Updated:  12/31/1969
University of Alabama at Birmingham
mi
from
Birmingham, AL
Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection
Randomized Clinical Trial of Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection in Very-Low-Birth-Weight Infants
Status: Enrolling
Updated: 12/31/1969
University of Alabama at Birmingham
mi
from
Birmingham, AL
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Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection
Randomized Clinical Trial of Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection in Very-Low-Birth-Weight Infants
Status: Enrolling
Updated:  12/31/1969
George Washington University
mi
from
Washington,
Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection
Randomized Clinical Trial of Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection in Very-Low-Birth-Weight Infants
Status: Enrolling
Updated: 12/31/1969
George Washington University
mi
from
Washington,
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Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection
Randomized Clinical Trial of Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection in Very-Low-Birth-Weight Infants
Status: Enrolling
Updated:  12/31/1969
University of Miami
mi
from
Miami, FL
Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection
Randomized Clinical Trial of Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection in Very-Low-Birth-Weight Infants
Status: Enrolling
Updated: 12/31/1969
University of Miami
mi
from
Miami, FL
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Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection
Randomized Clinical Trial of Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection in Very-Low-Birth-Weight Infants
Status: Enrolling
Updated:  12/31/1969
Wayne State University
mi
from
Detroit, MI
Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection
Randomized Clinical Trial of Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection in Very-Low-Birth-Weight Infants
Status: Enrolling
Updated: 12/31/1969
Wayne State University
mi
from
Detroit, MI
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Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection
Randomized Clinical Trial of Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection in Very-Low-Birth-Weight Infants
Status: Enrolling
Updated:  12/31/1969
Case Western Reserve University, Rainbow Babies and Children's Hospital
mi
from
Cleveland, OH
Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection
Randomized Clinical Trial of Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection in Very-Low-Birth-Weight Infants
Status: Enrolling
Updated: 12/31/1969
Case Western Reserve University, Rainbow Babies and Children's Hospital
mi
from
Cleveland, OH
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Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection
Randomized Clinical Trial of Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection in Very-Low-Birth-Weight Infants
Status: Enrolling
Updated:  12/31/1969
University of Tennessee
mi
from
Memphis, TN
Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection
Randomized Clinical Trial of Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection in Very-Low-Birth-Weight Infants
Status: Enrolling
Updated: 12/31/1969
University of Tennessee
mi
from
Memphis, TN
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Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection
Randomized Clinical Trial of Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection in Very-Low-Birth-Weight Infants
Status: Enrolling
Updated:  12/31/1969
UT Southwestern Medical Center
mi
from
Dallas, TX
Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection
Randomized Clinical Trial of Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection in Very-Low-Birth-Weight Infants
Status: Enrolling
Updated: 12/31/1969
UT Southwestern Medical Center
mi
from
Dallas, TX
Click here to add this to my saved trials
Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection
Randomized Clinical Trial of Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection in Very-Low-Birth-Weight Infants
Status: Enrolling
Updated:  12/31/1969
University of Vermont
mi
from
Burlington, VT
Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection
Randomized Clinical Trial of Intravenous Immune Globulin (IVIG) to Prevent Neonatal Infection in Very-Low-Birth-Weight Infants
Status: Enrolling
Updated: 12/31/1969
University of Vermont
mi
from
Burlington, VT
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Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated:  12/31/1969
Stanford University
mi
from
Palo Alto, CA
Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated: 12/31/1969
Stanford University
mi
from
Palo Alto, CA
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Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated:  12/31/1969
Yale University
mi
from
New Haven, CT
Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated: 12/31/1969
Yale University
mi
from
New Haven, CT
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Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated:  12/31/1969
George Washington University
mi
from
Washington,
Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated: 12/31/1969
George Washington University
mi
from
Washington,
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Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated:  12/31/1969
University of Miami
mi
from
Miami, FL
Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated: 12/31/1969
University of Miami
mi
from
Miami, FL
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Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated:  12/31/1969
Emory University
mi
from
Atlanta, GA
Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated: 12/31/1969
Emory University
mi
from
Atlanta, GA
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Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated:  12/31/1969
Indiana University
mi
from
Indianapolis, IN
Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated: 12/31/1969
Indiana University
mi
from
Indianapolis, IN
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Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated:  12/31/1969
Wayne State University
mi
from
Detroit, MI
Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated: 12/31/1969
Wayne State University
mi
from
Detroit, MI
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Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated:  12/31/1969
University of New Mexico
mi
from
Albuquerque, NM
Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated: 12/31/1969
University of New Mexico
mi
from
Albuquerque, NM
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Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated:  12/31/1969
Cincinnati Children's Medical Center
mi
from
Cincinnati, OH
Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated: 12/31/1969
Cincinnati Children's Medical Center
mi
from
Cincinnati, OH
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Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated:  12/31/1969
Case Western Reserve University, Rainbow Babies and Children's Hospital
mi
from
Cleveland, OH
Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated: 12/31/1969
Case Western Reserve University, Rainbow Babies and Children's Hospital
mi
from
Cleveland, OH
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Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated:  12/31/1969
University of Tennessee
mi
from
Memphis, TN
Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated: 12/31/1969
University of Tennessee
mi
from
Memphis, TN
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Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated:  12/31/1969
UT Southwestern Medical Center
mi
from
Dallas, TX
Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated: 12/31/1969
UT Southwestern Medical Center
mi
from
Dallas, TX
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Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated:  12/31/1969
University of Vermont
mi
from
Burlington, VT
Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome
Efficacy and Safety of Exosurf Neonatal and Survanta for the Treatment of Respiratory Distress Syndrome
Status: Enrolling
Updated: 12/31/1969
University of Vermont
mi
from
Burlington, VT
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A Systematic Oral Care Program in Post-Mechanically Ventilated, Post-Intensive Care Patients
A Systematic Oral Care Program in Post-Mechanically Ventilated, Post-Intensive Care Patients
Status: Enrolling
Updated:  12/31/1969
Ohio State University
mi
from
Columbus, OH
A Systematic Oral Care Program in Post-Mechanically Ventilated, Post-Intensive Care Patients
A Systematic Oral Care Program in Post-Mechanically Ventilated, Post-Intensive Care Patients
Status: Enrolling
Updated: 12/31/1969
Ohio State University
mi
from
Columbus, OH
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Safe and Effective Shoulder Exercise Training in Manual Wheelchair Users With SCI
Safe and Effective Shoulder Exercise Training in Manual Wheelchair Users With SCI
Status: Enrolling
Updated:  12/31/1969
Univ of Minnesota
mi
from
Minneapolis, MN
Safe and Effective Shoulder Exercise Training in Manual Wheelchair Users With SCI
Safe and Effective Shoulder Exercise Training in Manual Wheelchair Users With SCI
Status: Enrolling
Updated: 12/31/1969
Univ of Minnesota
mi
from
Minneapolis, MN
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Lactic Acid Levels In Hypotensive Patients Without(Standard) and With Tourniquet
Lactic Acid Levels In Hypotensive Patients Without(Standard) and With Tourniquet
Status: Enrolling
Updated:  12/31/1969
Upstate Hospital Emergency Department
mi
from
Syracuse, NY
Lactic Acid Levels In Hypotensive Patients Without(Standard) and With Tourniquet
Lactic Acid Levels In Hypotensive Patients Without(Standard) and With Tourniquet
Status: Enrolling
Updated: 12/31/1969
Upstate Hospital Emergency Department
mi
from
Syracuse, NY
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Treadmill Training With Body Weight Support in Patients With Spinal Cord Injury
Body Weight Supported Ambulation Training After Spinal Cord Injury
Status: Enrolling
Updated:  6/23/2005
Upstate Medical University
mi
from
Miami, FL
Treadmill Training With Body Weight Support in Patients With Spinal Cord Injury
Body Weight Supported Ambulation Training After Spinal Cord Injury
Status: Enrolling
Updated: 6/23/2005
Upstate Medical University
mi
from
Miami, FL
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