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

ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated:  12/5/2016
University of South Alabama Dept. of Surgery
mi
from
Mobile, AL
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated: 12/5/2016
University of South Alabama Dept. of Surgery
mi
from
Mobile, AL
Click here to add this to my saved trials
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated:  12/5/2016
Lac & Usc Medical Center
mi
from
Los Angeles, CA
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated: 12/5/2016
Lac & Usc Medical Center
mi
from
Los Angeles, CA
Click here to add this to my saved trials
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated:  12/5/2016
Shands Burn Center at the University of Florida
mi
from
Gainsville, FL
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated: 12/5/2016
Shands Burn Center at the University of Florida
mi
from
Gainsville, FL
Click here to add this to my saved trials
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated:  12/5/2016
University of South Florida, Tampa General Hospital
mi
from
Tampa, FL
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated: 12/5/2016
University of South Florida, Tampa General Hospital
mi
from
Tampa, FL
Click here to add this to my saved trials
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated:  12/5/2016
Loyola University Medical Center
mi
from
Maywood, IL
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated: 12/5/2016
Loyola University Medical Center
mi
from
Maywood, IL
Click here to add this to my saved trials
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated:  12/5/2016
University of Kentucky Chandler Medical Center
mi
from
Lexington, KY
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated: 12/5/2016
University of Kentucky Chandler Medical Center
mi
from
Lexington, KY
Click here to add this to my saved trials
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated:  12/5/2016
Johns Hopkins Burn Center
mi
from
Baltimore, MD
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated: 12/5/2016
Johns Hopkins Burn Center
mi
from
Baltimore, MD
Click here to add this to my saved trials
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated:  12/5/2016
Brigham and Women's Hosp
mi
from
Boston, MA
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated: 12/5/2016
Brigham and Women's Hosp
mi
from
Boston, MA
Click here to add this to my saved trials
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated:  12/5/2016
University of Missouri Health Care
mi
from
Columbia, MO
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated: 12/5/2016
University of Missouri Health Care
mi
from
Columbia, MO
Click here to add this to my saved trials
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated:  12/5/2016
Acute & Critical Care Surgery Barnes Jewish Hospital, Washington University Medical Center
mi
from
St. Louis, MO
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated: 12/5/2016
Acute & Critical Care Surgery Barnes Jewish Hospital, Washington University Medical Center
mi
from
St. Louis, MO
Click here to add this to my saved trials
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated:  12/5/2016
University of Rochester
mi
from
Rochester, NY
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated: 12/5/2016
University of Rochester
mi
from
Rochester, NY
Click here to add this to my saved trials
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated:  12/5/2016
MetroHealth Med Ctr
mi
from
Cleveland, OH
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated: 12/5/2016
MetroHealth Med Ctr
mi
from
Cleveland, OH
Click here to add this to my saved trials
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated:  12/5/2016
Western Pennsylvania Hospital
mi
from
Pittsburgh, PA
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated: 12/5/2016
Western Pennsylvania Hospital
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated:  12/5/2016
John S. Dunn Sr. Burn Center
mi
from
Houston, TX
ACCS (Amnion-derived Cellular Cytokine Solution) Versus Standard Care In Treating Partial Thickness Burns
Phase I/II Randomized Blinded Safety, Dose-determining Efficacy Trial Comparing Amnion-derived Cellular Cytokine Solution in 3 Different Regimens With Standard Care 0.9% Sodium Chloride in the Topical Treatment of Partial-thickness Burns
Status: Enrolling
Updated: 12/5/2016
John S. Dunn Sr. Burn Center
mi
from
Houston, TX
Click here to add this to my saved trials
Effect of IV Acetaminophen on Patients in the Neurocritical Care Unit
Status: Enrolling
Updated:  12/8/2016
University of Utah
mi
from
Salt Lake City, UT
Effect of IV Acetaminophen on Patients in the Neurocritical Care Unit
Status: Enrolling
Updated: 12/8/2016
University of Utah
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
MRI Temperature Mapping of the Prostate and Urogenital Pelvis Cooled by an Endorectal Balloon
MRI (Magnetic Resonance Imaging) Temperature Mapping of the Prostate and Urogenital Pelvis Cooled by an Endorectal Balloon
Status: Enrolling
Updated:  12/12/2016
University of California, Irvine Medical Center
mi
from
Orange, CA
MRI Temperature Mapping of the Prostate and Urogenital Pelvis Cooled by an Endorectal Balloon
MRI (Magnetic Resonance Imaging) Temperature Mapping of the Prostate and Urogenital Pelvis Cooled by an Endorectal Balloon
Status: Enrolling
Updated: 12/12/2016
University of California, Irvine Medical Center
mi
from
Orange, CA
Click here to add this to my saved trials
Laryngectomy Education
Effect of Total Laryngectomy Preoperative Education on Postoperative Complications and Unplanned Hospital Readmission
Status: Enrolling
Updated:  12/12/2016
Washington University School of Medicine
mi
from
St. Louis, MO
Laryngectomy Education
Effect of Total Laryngectomy Preoperative Education on Postoperative Complications and Unplanned Hospital Readmission
Status: Enrolling
Updated: 12/12/2016
Washington University School of Medicine
mi
from
St. Louis, MO
Click here to add this to my saved trials
Evaluating Erythropoietin as an Indicator for Possible Kidney Injury After Cardiac Surgery
EPO: A Renal Biomarker After Cardiac Surgery
Status: Enrolling
Updated:  12/14/2016
University of Michigan Hospital
mi
from
Ann Arbor, MI
Evaluating Erythropoietin as an Indicator for Possible Kidney Injury After Cardiac Surgery
EPO: A Renal Biomarker After Cardiac Surgery
Status: Enrolling
Updated: 12/14/2016
University of Michigan Hospital
mi
from
Ann Arbor, MI
Click here to add this to my saved trials
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated:  12/22/2016
Denver Health and Hospital Authority
mi
from
Denver, CO
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated: 12/22/2016
Denver Health and Hospital Authority
mi
from
Denver, CO
Click here to add this to my saved trials
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated:  12/22/2016
St. Joseph's Hospital
mi
from
Tampa, FL
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated: 12/22/2016
St. Joseph's Hospital
mi
from
Tampa, FL
Click here to add this to my saved trials
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated:  12/22/2016
Tampa General Hospital
mi
from
Tampa, FL
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated: 12/22/2016
Tampa General Hospital
mi
from
Tampa, FL
Click here to add this to my saved trials
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated:  12/22/2016
Methodist Hospital
mi
from
Indianapolis, IN
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated: 12/22/2016
Methodist Hospital
mi
from
Indianapolis, IN
Click here to add this to my saved trials
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated:  12/22/2016
University of Maryland/ R Cowley Adams Shock Trauma Center
mi
from
Baltimore, MD
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated: 12/22/2016
University of Maryland/ R Cowley Adams Shock Trauma Center
mi
from
Baltimore, MD
Click here to add this to my saved trials
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated:  12/22/2016
Spectrum Health/Orthopaedic Institutes of Michigan
mi
from
Grand Rapids, MI
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated: 12/22/2016
Spectrum Health/Orthopaedic Institutes of Michigan
mi
from
Grand Rapids, MI
Click here to add this to my saved trials
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated:  12/22/2016
Carolinas Medical Center
mi
from
Charlotte, NC
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated: 12/22/2016
Carolinas Medical Center
mi
from
Charlotte, NC
Click here to add this to my saved trials
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated:  12/22/2016
Wake Forest Baprtist Medicla Center
mi
from
Winston-Salem, NC
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated: 12/22/2016
Wake Forest Baprtist Medicla Center
mi
from
Winston-Salem, NC
Click here to add this to my saved trials
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated:  12/22/2016
Metro Health
mi
from
Cleveland, OH
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated: 12/22/2016
Metro Health
mi
from
Cleveland, OH
Click here to add this to my saved trials
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated:  12/22/2016
Vanderbilt Medical Center
mi
from
Nashville, TN
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated: 12/22/2016
Vanderbilt Medical Center
mi
from
Nashville, TN
Click here to add this to my saved trials
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated:  12/22/2016
University of Texas Health Science Center at Houston
mi
from
Houston, TX
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated: 12/22/2016
University of Texas Health Science Center at Houston
mi
from
Houston, TX
Click here to add this to my saved trials
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated:  12/22/2016
Inova Fairfax Hospital
mi
from
Falls Church, VA
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated: 12/22/2016
Inova Fairfax Hospital
mi
from
Falls Church, VA
Click here to add this to my saved trials
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated:  12/22/2016
Hennepin County Medical Center
mi
from
Minneapolis, MN
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Improving Activity and Quality of Life Following Orthopaedic Trauma: The Trauma Collaborative Care Study (TCCS)
Status: Enrolling
Updated: 12/22/2016
Hennepin County Medical Center
mi
from
Minneapolis, MN
Click here to add this to my saved trials
Effect of Intrathoracic Pressure Regulation on Decreased Cerebral Perfusion (4hour)
Physiological Effects of Intrathoracic Pressure Regulation in Patients With Decreased Cerebral Perfusion Due to Brain Injury or Intracranial Pathology (4 Hour Use)
Status: Enrolling
Updated:  12/29/2016
University of Texas Health Science Center at San Antonio
mi
from
San Antonio, TX
Effect of Intrathoracic Pressure Regulation on Decreased Cerebral Perfusion (4hour)
Physiological Effects of Intrathoracic Pressure Regulation in Patients With Decreased Cerebral Perfusion Due to Brain Injury or Intracranial Pathology (4 Hour Use)
Status: Enrolling
Updated: 12/29/2016
University of Texas Health Science Center at San Antonio
mi
from
San Antonio, TX
Click here to add this to my saved trials
Assess the Ability of Electrical Cardiometry to Trend Hemodynamic Variables During Dexmedetomidine Sedation
A Pilot Study to Assess the Ability of Non-invasive Bio-impedance Cardiac Monitoring to Detect and Trend Hemodynamic Variables During Dexmedetomidine (DEX) Sedation in Children for Radiology Procedures
Status: Enrolling
Updated:  1/4/2017
Children' Hospital Boston
mi
from
Boston, MA
Assess the Ability of Electrical Cardiometry to Trend Hemodynamic Variables During Dexmedetomidine Sedation
A Pilot Study to Assess the Ability of Non-invasive Bio-impedance Cardiac Monitoring to Detect and Trend Hemodynamic Variables During Dexmedetomidine (DEX) Sedation in Children for Radiology Procedures
Status: Enrolling
Updated: 1/4/2017
Children' Hospital Boston
mi
from
Boston, MA
Click here to add this to my saved trials
Emergency Department Initiated Tobacco Treatment (EDITT)
Emergency Department Initiated Tobacco Treatment (EDITT)
Status: Enrolling
Updated:  1/10/2017
Cooper University Hospital
mi
from
Camden, NJ
Emergency Department Initiated Tobacco Treatment (EDITT)
Emergency Department Initiated Tobacco Treatment (EDITT)
Status: Enrolling
Updated: 1/10/2017
Cooper University Hospital
mi
from
Camden, NJ
Click here to add this to my saved trials
Home-Based Diagnosis and Management of Sleep-Related Breathing Disorders in Spinal Cord Injury
Home-Based Diagnosis and Management of Sleep-Related Breathing Disorders in Spinal Cord Injury
Status: Enrolling
Updated:  1/10/2017
University of Michigan Health System
mi
from
Ann Arbor, MI
Home-Based Diagnosis and Management of Sleep-Related Breathing Disorders in Spinal Cord Injury
Home-Based Diagnosis and Management of Sleep-Related Breathing Disorders in Spinal Cord Injury
Status: Enrolling
Updated: 1/10/2017
University of Michigan Health System
mi
from
Ann Arbor, MI
Click here to add this to my saved trials
DIVAs Perception: Difficult IV Access - Assessment of Patient Understanding
Assessment of Patient Understanding and Preference of Rescue Venous Access When Shown a Narrated Video Vignette Versus Traditional Paper Information Sheet
Status: Enrolling
Updated:  1/10/2017
Hospital of the University of Pennsylvania
mi
from
Philadelphia, PA
DIVAs Perception: Difficult IV Access - Assessment of Patient Understanding
Assessment of Patient Understanding and Preference of Rescue Venous Access When Shown a Narrated Video Vignette Versus Traditional Paper Information Sheet
Status: Enrolling
Updated: 1/10/2017
Hospital of the University of Pennsylvania
mi
from
Philadelphia, PA
Click here to add this to my saved trials
Study of Glutamate and Glutamine Metabolism in Burn Patients Receiving Enteral or Parenteral Nutrition
Study of Glutamate and Glutamine Metabolism in Burn Patients Receiving Enteral or Parenteral Nutrition
Status: Enrolling
Updated:  1/12/2017
Massachusetts General Hospital Burn Unit
mi
from
Boston, MA
Study of Glutamate and Glutamine Metabolism in Burn Patients Receiving Enteral or Parenteral Nutrition
Study of Glutamate and Glutamine Metabolism in Burn Patients Receiving Enteral or Parenteral Nutrition
Status: Enrolling
Updated: 1/12/2017
Massachusetts General Hospital Burn Unit
mi
from
Boston, MA
Click here to add this to my saved trials
Randomized Clinical Trial of Skin Closure With Staples Versus Suture
Randomized Controlled Phase IIB Trial Evaluating Wound Complication Rate After Skin Closure With Staples Versus Subcuticular Suture in Patients With BMI >=30
Status: Enrolling
Updated:  1/12/2017
Washington University School of Medicine and Barnes Jewish Hospital
mi
from
St Louis, MO
Randomized Clinical Trial of Skin Closure With Staples Versus Suture
Randomized Controlled Phase IIB Trial Evaluating Wound Complication Rate After Skin Closure With Staples Versus Subcuticular Suture in Patients With BMI >=30
Status: Enrolling
Updated: 1/12/2017
Washington University School of Medicine and Barnes Jewish Hospital
mi
from
St Louis, MO
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Animal Assisted Activity Program on Patients and Staff on an Inpatient Surgical Oncology Unit
Caring Canines: Outcomes From an Animal Assisted Activity Program on Patients and Staff on an Inpatient Surgical Oncology Unit
Status: Enrolling
Updated:  1/12/2017
Memorial Sloan Kettering Cancer Center
mi
from
New York, NY
Animal Assisted Activity Program on Patients and Staff on an Inpatient Surgical Oncology Unit
Caring Canines: Outcomes From an Animal Assisted Activity Program on Patients and Staff on an Inpatient Surgical Oncology Unit
Status: Enrolling
Updated: 1/12/2017
Memorial Sloan Kettering Cancer Center
mi
from
New York, NY
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Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated:  1/19/2017
GSK Investigational Site
mi
from
Little Rock, AR
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated: 1/19/2017
GSK Investigational Site
mi
from
Little Rock, AR
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Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated:  1/19/2017
GSK Investigational Site
mi
from
Glendale, CA
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated: 1/19/2017
GSK Investigational Site
mi
from
Glendale, CA
Click here to add this to my saved trials
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated:  1/19/2017
GSK Investigational Site
mi
from
Laguna Hills, CA
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated: 1/19/2017
GSK Investigational Site
mi
from
Laguna Hills, CA
Click here to add this to my saved trials
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated:  1/19/2017
GSK Investigational Site
mi
from
Los Angeles, CA
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated: 1/19/2017
GSK Investigational Site
mi
from
Los Angeles, CA
Click here to add this to my saved trials
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated:  1/19/2017
GSK Investigational Site
mi
from
Pasadena, CA
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated: 1/19/2017
GSK Investigational Site
mi
from
Pasadena, CA
Click here to add this to my saved trials
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated:  1/19/2017
GSK Investigational Site
mi
from
Boca Raton, FL
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated: 1/19/2017
GSK Investigational Site
mi
from
Boca Raton, FL
Click here to add this to my saved trials
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated:  1/19/2017
GSK Investigational Site
mi
from
Chicago, IL
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated: 1/19/2017
GSK Investigational Site
mi
from
Chicago, IL
Click here to add this to my saved trials
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated:  1/19/2017
GSK Investigational Site
mi
from
Omaha, NE
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated: 1/19/2017
GSK Investigational Site
mi
from
Omaha, NE
Click here to add this to my saved trials
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated:  1/19/2017
GSK Investigational Site
mi
from
Albany, NY
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated: 1/19/2017
GSK Investigational Site
mi
from
Albany, NY
Click here to add this to my saved trials
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated:  1/19/2017
GSK Investigational Site
mi
from
New York, NY
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated: 1/19/2017
GSK Investigational Site
mi
from
New York, NY
Click here to add this to my saved trials
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated:  1/19/2017
GSK Investigational Site
mi
from
Durham, NC
Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients
Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk
Status: Enrolling
Updated: 1/19/2017
GSK Investigational Site
mi
from
Durham, NC
Click here to add this to my saved trials