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

Effect of Fentanyl on Coughing and Recovery After Anesthesia With an LMA Laryngeal Mask Airway)for Airway Management
Randomized, Double-Blinded, Placebo-Controlled Study to Evaluate the Effect of Fentanyl on the Incidence of Coughing and Recovery After Propofol-Desflurane Anesthesia With an LMA for Airway Management
Status: Enrolling
Updated:  3/9/2016
Cedars-Sinai Medical Center
mi
from
Los Angeles, CA
Effect of Fentanyl on Coughing and Recovery After Anesthesia With an LMA Laryngeal Mask Airway)for Airway Management
Randomized, Double-Blinded, Placebo-Controlled Study to Evaluate the Effect of Fentanyl on the Incidence of Coughing and Recovery After Propofol-Desflurane Anesthesia With an LMA for Airway Management
Status: Enrolling
Updated: 3/9/2016
Cedars-Sinai Medical Center
mi
from
Los Angeles, CA
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Therapeutic Hypothermia for Severe Acute Pancreatitis
Therapeutic Hypothermia for Severe Acute Pancreatitis: A Clinical Model for "Suspended Inflammation"
Status: Enrolling
Updated:  3/10/2016
NYU Medical Center
mi
from
New York, NY
Therapeutic Hypothermia for Severe Acute Pancreatitis
Therapeutic Hypothermia for Severe Acute Pancreatitis: A Clinical Model for "Suspended Inflammation"
Status: Enrolling
Updated: 3/10/2016
NYU Medical Center
mi
from
New York, NY
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Electrical Activity of Diaphragm as a Means to Predict Extubation Success in Preterm Infants
A Prospective Study of Diaphragmatic Electrical Activity in Preterm Infants as a Means to Predict Extubation Success
Status: Enrolling
Updated:  3/10/2016
Dartmouth Hitchcock Medcial Center
mi
from
Lebanon, NH
Electrical Activity of Diaphragm as a Means to Predict Extubation Success in Preterm Infants
A Prospective Study of Diaphragmatic Electrical Activity in Preterm Infants as a Means to Predict Extubation Success
Status: Enrolling
Updated: 3/10/2016
Dartmouth Hitchcock Medcial Center
mi
from
Lebanon, NH
Click here to add this to my saved trials
FES-Rowing Versus Zoledronic Acid to Improve Bone Health in Spinal Cord Injury (SCI)
FES-Rowing Versus Zoledronic Acid to Improve Bone Health in SCI: A Comparative Clinical Trial
Status: Enrolling
Updated:  3/11/2016
Boston VAMC
mi
from
Boston, MA
FES-Rowing Versus Zoledronic Acid to Improve Bone Health in Spinal Cord Injury (SCI)
FES-Rowing Versus Zoledronic Acid to Improve Bone Health in SCI: A Comparative Clinical Trial
Status: Enrolling
Updated: 3/11/2016
Boston VAMC
mi
from
Boston, MA
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FES-Rowing Versus Zoledronic Acid to Improve Bone Health in Spinal Cord Injury (SCI)
FES-Rowing Versus Zoledronic Acid to Improve Bone Health in SCI: A Comparative Clinical Trial
Status: Enrolling
Updated:  3/11/2016
Spaulding Rehab. Hospital
mi
from
Charlestown, MA
FES-Rowing Versus Zoledronic Acid to Improve Bone Health in Spinal Cord Injury (SCI)
FES-Rowing Versus Zoledronic Acid to Improve Bone Health in SCI: A Comparative Clinical Trial
Status: Enrolling
Updated: 3/11/2016
Spaulding Rehab. Hospital
mi
from
Charlestown, MA
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Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes in Newborn Brain Injury (NEATO)
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes Study
Status: Enrolling
Updated:  3/14/2016
Arkansas Children's Hospital Research Institute
mi
from
Little Rock, AR
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes in Newborn Brain Injury (NEATO)
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes Study
Status: Enrolling
Updated: 3/14/2016
Arkansas Children's Hospital Research Institute
mi
from
Little Rock, AR
Click here to add this to my saved trials
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes in Newborn Brain Injury (NEATO)
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes Study
Status: Enrolling
Updated:  3/14/2016
Kaiser Permanente Santa Clara
mi
from
Santa Clara, CA
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes in Newborn Brain Injury (NEATO)
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes Study
Status: Enrolling
Updated: 3/14/2016
Kaiser Permanente Santa Clara
mi
from
Santa Clara, CA
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Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes in Newborn Brain Injury (NEATO)
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes Study
Status: Enrolling
Updated:  3/14/2016
Children's National Medical Center
mi
from
Washington DC,
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes in Newborn Brain Injury (NEATO)
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes Study
Status: Enrolling
Updated: 3/14/2016
Children's National Medical Center
mi
from
Washington DC,
Click here to add this to my saved trials
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes in Newborn Brain Injury (NEATO)
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes Study
Status: Enrolling
Updated:  3/14/2016
Washington University
mi
from
St. Louis, MO
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes in Newborn Brain Injury (NEATO)
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes Study
Status: Enrolling
Updated: 3/14/2016
Washington University
mi
from
St. Louis, MO
Click here to add this to my saved trials
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes in Newborn Brain Injury (NEATO)
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes Study
Status: Enrolling
Updated:  3/14/2016
Seattle Children's Hospital
mi
from
Seattle, WA
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes in Newborn Brain Injury (NEATO)
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes Study
Status: Enrolling
Updated: 3/14/2016
Seattle Children's Hospital
mi
from
Seattle, WA
Click here to add this to my saved trials
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes in Newborn Brain Injury (NEATO)
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes Study
Status: Enrolling
Updated:  3/14/2016
Stanford University
mi
from
Palo Alto, CA
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes in Newborn Brain Injury (NEATO)
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes Study
Status: Enrolling
Updated: 3/14/2016
Stanford University
mi
from
Palo Alto, CA
Click here to add this to my saved trials
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes in Newborn Brain Injury (NEATO)
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes Study
Status: Enrolling
Updated:  3/14/2016
UCSF
mi
from
San Francisco, CA
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes in Newborn Brain Injury (NEATO)
Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes Study
Status: Enrolling
Updated: 3/14/2016
UCSF
mi
from
San Francisco, CA
Click here to add this to my saved trials
Phase I Rising-dose Study to Assess Tolerability, Safety, Pharmacokinetics, Pharmacodynamics of AR09
A Phase I, Randomized, Double-blind, Placebo-controlled, Rising-dose Study to Assess the Tolerability, Safety, Pharmacokinetics, and Pharmacodynamics of Single IV Doses of AR09 in Healthy Subjects
Status: Enrolling
Updated:  3/14/2016
Duke Clinical Research Unit
mi
from
Durham, NC
Phase I Rising-dose Study to Assess Tolerability, Safety, Pharmacokinetics, Pharmacodynamics of AR09
A Phase I, Randomized, Double-blind, Placebo-controlled, Rising-dose Study to Assess the Tolerability, Safety, Pharmacokinetics, and Pharmacodynamics of Single IV Doses of AR09 in Healthy Subjects
Status: Enrolling
Updated: 3/14/2016
Duke Clinical Research Unit
mi
from
Durham, NC
Click here to add this to my saved trials
Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Status: Enrolling
Updated:  3/14/2016
Palo Alto Medical Foundation
mi
from
Palo Alto, CA
Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Status: Enrolling
Updated: 3/14/2016
Palo Alto Medical Foundation
mi
from
Palo Alto, CA
Click here to add this to my saved trials
Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Status: Enrolling
Updated:  3/14/2016
Alvarado Orthopedic Clinic
mi
from
San Diego, CA
Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Status: Enrolling
Updated: 3/14/2016
Alvarado Orthopedic Clinic
mi
from
San Diego, CA
Click here to add this to my saved trials
Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Status: Enrolling
Updated:  3/14/2016
American Health Network
mi
from
Avon, IN
Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Status: Enrolling
Updated: 3/14/2016
American Health Network
mi
from
Avon, IN
Click here to add this to my saved trials
Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Status: Enrolling
Updated:  3/14/2016
Raliegh Orthopedic Research Foundation
mi
from
Raleigh, NC
Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Status: Enrolling
Updated: 3/14/2016
Raliegh Orthopedic Research Foundation
mi
from
Raleigh, NC
Click here to add this to my saved trials
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
University of South Alabama Medical Center
mi
from
Mobile, AL
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
University of South Alabama Medical Center
mi
from
Mobile, AL
Click here to add this to my saved trials
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
Arrowhead Regional Medical Center
mi
from
Redlands, CA
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
Arrowhead Regional Medical Center
mi
from
Redlands, CA
Click here to add this to my saved trials
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
Shands Burn Center at University of Florida
mi
from
Gainesville, FL
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
Shands Burn Center at University of Florida
mi
from
Gainesville, FL
Click here to add this to my saved trials
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
Loyola University Medical Center
mi
from
Maywood, IL
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
Loyola University Medical Center
mi
from
Maywood, IL
Click here to add this to my saved trials
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
The Plastic Surgery Institute - Southern Illinois Univ. School of Medicine
mi
from
Springfield, IL
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
The Plastic Surgery Institute - Southern Illinois Univ. School of Medicine
mi
from
Springfield, IL
Click here to add this to my saved trials
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
University of Kansas Medical Center
mi
from
Kansas City, KA
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
University of Kansas Medical Center
mi
from
Kansas City, KA
Click here to add this to my saved trials
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
Johns Hopkins Burn Center
mi
from
Baltimore, MD
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
Johns Hopkins Burn Center
mi
from
Baltimore, MD
Click here to add this to my saved trials
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
University of Missouri Healthcare - Dept. of Surgery
mi
from
Columbia, MO
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
University of Missouri Healthcare - Dept. of Surgery
mi
from
Columbia, MO
Click here to add this to my saved trials
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
Wake Forest University - Department of General Surgery
mi
from
Winston-Salem, NC
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
Wake Forest University - Department of General Surgery
mi
from
Winston-Salem, NC
Click here to add this to my saved trials
Postoperative Cognitive Decline, Inflammation, and Plasma Levels of Beta-amyloids
Postoperative Cognitive Decline, Inflammation, and Plasma Levels of Beta-amyloids.
Status: Enrolling
Updated:  3/15/2016
NYU School of Medicine
mi
from
New York City, NY
Postoperative Cognitive Decline, Inflammation, and Plasma Levels of Beta-amyloids
Postoperative Cognitive Decline, Inflammation, and Plasma Levels of Beta-amyloids.
Status: Enrolling
Updated: 3/15/2016
NYU School of Medicine
mi
from
New York City, NY
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Code Status Video in the Intensive Care Unit: Video Assisted Patient Education
Pilot Study to Determine Effectiveness and Acceptance of a Code Status Video in the ICU
Status: Enrolling
Updated:  3/15/2016
The Mayo Clinic
mi
from
Rochester, MN
Code Status Video in the Intensive Care Unit: Video Assisted Patient Education
Pilot Study to Determine Effectiveness and Acceptance of a Code Status Video in the ICU
Status: Enrolling
Updated: 3/15/2016
The Mayo Clinic
mi
from
Rochester, MN
Click here to add this to my saved trials
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated:  3/15/2016
St. Joseph's Hospital and Medical Center
mi
from
Phoenix, AZ
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated: 3/15/2016
St. Joseph's Hospital and Medical Center
mi
from
Phoenix, AZ
Click here to add this to my saved trials
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated:  3/15/2016
University of Cincinnati Mayfield Clinic and Spine Institute
mi
from
Cincinnati, OH
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated: 3/15/2016
University of Cincinnati Mayfield Clinic and Spine Institute
mi
from
Cincinnati, OH
Click here to add this to my saved trials
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated:  3/15/2016
Thomas Jefferson University Hospital
mi
from
Philadelphia, PA
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated: 3/15/2016
Thomas Jefferson University Hospital
mi
from
Philadelphia, PA
Click here to add this to my saved trials
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated:  3/15/2016
Univ.of Virginia Health System
mi
from
Charlottesville, VA
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated: 3/15/2016
Univ.of Virginia Health System
mi
from
Charlottesville, VA
Click here to add this to my saved trials
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated:  3/15/2016
University of Washington; Harborview Medical Center
mi
from
Seattle, WA
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated: 3/15/2016
University of Washington; Harborview Medical Center
mi
from
Seattle, WA
Click here to add this to my saved trials
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated:  3/15/2016
Sunnybrooke Health Sciences Centre
mi
from
Toronto,
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated: 3/15/2016
Sunnybrooke Health Sciences Centre
mi
from
Toronto,
Click here to add this to my saved trials
Cognitive Protection - Dexmedetomidine and Cognitive Reserve
Cognitive Protection - Dexmedetomidine and Cognitive Reserve
Status: Enrolling
Updated:  3/16/2016
Icahn School of Medicine at Mount Sinai
mi
from
New York, NY
Cognitive Protection - Dexmedetomidine and Cognitive Reserve
Cognitive Protection - Dexmedetomidine and Cognitive Reserve
Status: Enrolling
Updated: 3/16/2016
Icahn School of Medicine at Mount Sinai
mi
from
New York, NY
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Systematic Team Approach to Guide Early Mobilization in Surgical Intensive Care Unit Patients
Effects of a Systematic Team Approach to Guide Early Mobilization in Surgical ICU Patients
Status: Enrolling
Updated:  3/16/2016
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Systematic Team Approach to Guide Early Mobilization in Surgical Intensive Care Unit Patients
Effects of a Systematic Team Approach to Guide Early Mobilization in Surgical ICU Patients
Status: Enrolling
Updated: 3/16/2016
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
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Systematic Team Approach to Guide Early Mobilization in Surgical Intensive Care Unit Patients
Effects of a Systematic Team Approach to Guide Early Mobilization in Surgical ICU Patients
Status: Enrolling
Updated:  3/16/2016
Massachusetts General Hospital
mi
from
Boston, MA
Systematic Team Approach to Guide Early Mobilization in Surgical Intensive Care Unit Patients
Effects of a Systematic Team Approach to Guide Early Mobilization in Surgical ICU Patients
Status: Enrolling
Updated: 3/16/2016
Massachusetts General Hospital
mi
from
Boston, MA
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Systematic Team Approach to Guide Early Mobilization in Surgical Intensive Care Unit Patients
Effects of a Systematic Team Approach to Guide Early Mobilization in Surgical ICU Patients
Status: Enrolling
Updated:  3/16/2016
University of Massachusetts
mi
from
Worcester, MA
Systematic Team Approach to Guide Early Mobilization in Surgical Intensive Care Unit Patients
Effects of a Systematic Team Approach to Guide Early Mobilization in Surgical ICU Patients
Status: Enrolling
Updated: 3/16/2016
University of Massachusetts
mi
from
Worcester, MA
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Systematic Team Approach to Guide Early Mobilization in Surgical Intensive Care Unit Patients
Effects of a Systematic Team Approach to Guide Early Mobilization in Surgical ICU Patients
Status: Enrolling
Updated:  3/16/2016
University of Salzburg
mi
from
Salzburg,
Systematic Team Approach to Guide Early Mobilization in Surgical Intensive Care Unit Patients
Effects of a Systematic Team Approach to Guide Early Mobilization in Surgical ICU Patients
Status: Enrolling
Updated: 3/16/2016
University of Salzburg
mi
from
Salzburg,
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Effects of Frailty, Sarcopenia and Muscle Wasting on Outcomes of Patients in the Surgical Intensive Care Unit
Ultrasound Assessment of Muscle to Quantify Frailty.
Status: Enrolling
Updated:  3/16/2016
Massachusetts General Hospital
mi
from
Boston, MA
Effects of Frailty, Sarcopenia and Muscle Wasting on Outcomes of Patients in the Surgical Intensive Care Unit
Ultrasound Assessment of Muscle to Quantify Frailty.
Status: Enrolling
Updated: 3/16/2016
Massachusetts General Hospital
mi
from
Boston, MA
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Wound Dressings For Split-Thickness Skin Graft Donor Sites in Patients Undergoing Surgery
A Comparative Study of Dressings for Split-Thickness Skin Graft Donor Sites.
Status: Enrolling
Updated:  3/16/2016
Ohio State University Medical Center
mi
from
Columbus, OH
Wound Dressings For Split-Thickness Skin Graft Donor Sites in Patients Undergoing Surgery
A Comparative Study of Dressings for Split-Thickness Skin Graft Donor Sites.
Status: Enrolling
Updated: 3/16/2016
Ohio State University Medical Center
mi
from
Columbus, OH
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Comparison of ProSeal Laryngeal Mask Airway to Laryngeal Mask Airway Supreme
A Randomized Controlled Trial Comparing the ProSeal Laryngeal Mask Airway With the Laryngeal Mask Airway Supreme in Mechanically Ventilated Patients
Status: Enrolling
Updated:  3/17/2016
PennState Hershey Milton S. Hershey Medical Center
mi
from
Hershey, PA
Comparison of ProSeal Laryngeal Mask Airway to Laryngeal Mask Airway Supreme
A Randomized Controlled Trial Comparing the ProSeal Laryngeal Mask Airway With the Laryngeal Mask Airway Supreme in Mechanically Ventilated Patients
Status: Enrolling
Updated: 3/17/2016
PennState Hershey Milton S. Hershey Medical Center
mi
from
Hershey, PA
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Comparing Hemodynamic Changes for Intubation With Shikani Intubating Stylet and Macintosh Laryngoscope
Status: Enrolling
Updated:  3/17/2016
PennState Hershey Medical Center
mi
from
Hershey, PA
Comparing Hemodynamic Changes for Intubation With Shikani Intubating Stylet and Macintosh Laryngoscope
Status: Enrolling
Updated: 3/17/2016
PennState Hershey Medical Center
mi
from
Hershey, PA
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Effectiveness of Controlled-Release Morphine for Chronic Neuropathic Pain After Spinal Cord Injury
Effectiveness of Controlled-Release Morphine for Chronic Neuropathic Pain After Spinal Cord Injury
Status: Enrolling
Updated:  3/18/2016
Mount Sinai School of Medicine
mi
from
New York, NY
Effectiveness of Controlled-Release Morphine for Chronic Neuropathic Pain After Spinal Cord Injury
Effectiveness of Controlled-Release Morphine for Chronic Neuropathic Pain After Spinal Cord Injury
Status: Enrolling
Updated: 3/18/2016
Mount Sinai School of Medicine
mi
from
New York, NY
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Efficacy and Safety of Zoledronic Acid in Acute Spinal Cord Injury: Prevention of Bone Loss
Efficacy and Safety of Zoledronic Acid in Acute Spinal Cord Injury: Prevention of Bone Loss
Status: Enrolling
Updated:  3/21/2016
Rehabilitation Institute of Chicago
mi
from
Chicago, IL
Efficacy and Safety of Zoledronic Acid in Acute Spinal Cord Injury: Prevention of Bone Loss
Efficacy and Safety of Zoledronic Acid in Acute Spinal Cord Injury: Prevention of Bone Loss
Status: Enrolling
Updated: 3/21/2016
Rehabilitation Institute of Chicago
mi
from
Chicago, IL
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Study of A Long Lasting Local Anesthestic for Hand, Wrist or Finger Surgery
Exparel (Bupivacaine Liposome Injectable Suspension) for Distal Upper Extremity Blocks in Orthopedic Surgery
Status: Enrolling
Updated:  3/21/2016
Ochsner Clinic Foundation
mi
from
New Orleans, LA
Study of A Long Lasting Local Anesthestic for Hand, Wrist or Finger Surgery
Exparel (Bupivacaine Liposome Injectable Suspension) for Distal Upper Extremity Blocks in Orthopedic Surgery
Status: Enrolling
Updated: 3/21/2016
Ochsner Clinic Foundation
mi
from
New Orleans, LA
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Comparing Two Injection Sites of Local Anesthetic for Hand Surgery
A Comparison Of Distal Peripheral Nerve Blockade Versus Traditional Proximal Approaches For Hand Surgery
Status: Enrolling
Updated:  3/21/2016
Ochsner Clinic Foundation
mi
from
New Orleans, LA
Comparing Two Injection Sites of Local Anesthetic for Hand Surgery
A Comparison Of Distal Peripheral Nerve Blockade Versus Traditional Proximal Approaches For Hand Surgery
Status: Enrolling
Updated: 3/21/2016
Ochsner Clinic Foundation
mi
from
New Orleans, LA
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Non-inferiority Trial of Oral Tranexamic Acid vs. Intravenous Tranexamic Acid in Joint Replacement Surgery
Non-inferiority Trial of Oral Tranexamic Acid (OTA) vs. Intravenous Tranexamic Acid (IVTA) to Prevent Blood Loss in Joint Replacement Surgery
Status: Enrolling
Updated:  3/21/2016
New England Baptist Hospital
mi
from
Boston, MA
Non-inferiority Trial of Oral Tranexamic Acid vs. Intravenous Tranexamic Acid in Joint Replacement Surgery
Non-inferiority Trial of Oral Tranexamic Acid (OTA) vs. Intravenous Tranexamic Acid (IVTA) to Prevent Blood Loss in Joint Replacement Surgery
Status: Enrolling
Updated: 3/21/2016
New England Baptist Hospital
mi
from
Boston, MA
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Clinical Study of Gene-Eden-VIR/Novirin
Retrospective Chart Review of Gene-Eden-VIR/Novirin
Status: Enrolling
Updated:  3/21/2016
The Center for the Biology of Chronic Disease
mi
from
Valley Cottage, NY
Clinical Study of Gene-Eden-VIR/Novirin
Retrospective Chart Review of Gene-Eden-VIR/Novirin
Status: Enrolling
Updated: 3/21/2016
The Center for the Biology of Chronic Disease
mi
from
Valley Cottage, NY
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Acute Respiratory Distress Syndrome Clinical Network (ARDSNet)
Acute Respiratory Distress Syndrome Clinical Network (ARDSNet)
Status: Enrolling
Updated:  3/22/2016
University of California
mi
from
San Francisco, CA
Acute Respiratory Distress Syndrome Clinical Network (ARDSNet)
Acute Respiratory Distress Syndrome Clinical Network (ARDSNet)
Status: Enrolling
Updated: 3/22/2016
University of California
mi
from
San Francisco, CA
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