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

Control of Major Bleeding After Trauma Study
A Prospective, Randomized Comparison of Fresh Frozen Plasma Versus Standard Crystalloid Intravenous Fluid as Initial Resuscitation Fluid
Status: Enrolling
Updated:  12/31/1969
Denver Health Medical Center
mi
from
Denver, CO
Control of Major Bleeding After Trauma Study
A Prospective, Randomized Comparison of Fresh Frozen Plasma Versus Standard Crystalloid Intravenous Fluid as Initial Resuscitation Fluid
Status: Enrolling
Updated: 12/31/1969
Denver Health Medical Center
mi
from
Denver, CO
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Cromolyn Detection of Silent Aspiration
Development and Validation of Test for Gastro-esophageal Reflux and Aspiration
Status: Enrolling
Updated:  12/31/1969
UCSF Airway Clinical Research Center
mi
from
San Francisco, CA
Cromolyn Detection of Silent Aspiration
Development and Validation of Test for Gastro-esophageal Reflux and Aspiration
Status: Enrolling
Updated: 12/31/1969
UCSF Airway Clinical Research Center
mi
from
San Francisco, CA
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Hyperbaric Treatment of Traumatic Brain Injury (TBI)
Phase 1-2 Study of Hyperbaric Treatment of Traumatic Brain Injury
Status: Enrolling
Updated:  12/31/1969
Jupiter Medical Center
mi
from
Jupiter, FL
Hyperbaric Treatment of Traumatic Brain Injury (TBI)
Phase 1-2 Study of Hyperbaric Treatment of Traumatic Brain Injury
Status: Enrolling
Updated: 12/31/1969
Jupiter Medical Center
mi
from
Jupiter, FL
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Evaluation of the Effectiveness of tDCS in the Management of Perioperative Pain
Evaluation of the Effectiveness of tDCS in the Management of Perioperative Pain
Status: Enrolling
Updated:  12/31/1969
Brain Stimulation Laboratory, Institute of Psychiatry
mi
from
Charleston, SC
Evaluation of the Effectiveness of tDCS in the Management of Perioperative Pain
Evaluation of the Effectiveness of tDCS in the Management of Perioperative Pain
Status: Enrolling
Updated: 12/31/1969
Brain Stimulation Laboratory, Institute of Psychiatry
mi
from
Charleston, SC
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Marcaine Use in Laparoscopic Gynecological Surgery
A Comparative Trial of Marcaine Administration in Laparoscopic Gynecologic Surgery Using Either a Pre- or Post-operative Injection.
Status: Enrolling
Updated:  12/31/1969
Weill-Cornell Medical College
mi
from
New York, NY
Marcaine Use in Laparoscopic Gynecological Surgery
A Comparative Trial of Marcaine Administration in Laparoscopic Gynecologic Surgery Using Either a Pre- or Post-operative Injection.
Status: Enrolling
Updated: 12/31/1969
Weill-Cornell Medical College
mi
from
New York, NY
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Pilot Study of the Safety of a Daily Ethanol Lock for Urinary Catheters in Critically Ill Children
Pilot Study of the Safety of a Daily Ethanol Lock for Urinary Catheters in Critically Ill Children
Status: Enrolling
Updated:  12/31/1969
Children's Helathcare of Atlanta at Egleston
mi
from
Atlanta, GA
Pilot Study of the Safety of a Daily Ethanol Lock for Urinary Catheters in Critically Ill Children
Pilot Study of the Safety of a Daily Ethanol Lock for Urinary Catheters in Critically Ill Children
Status: Enrolling
Updated: 12/31/1969
Children's Helathcare of Atlanta at Egleston
mi
from
Atlanta, GA
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Early Mobility for the Critically Injured Burn Patient
Early ICU Standardized Rehabilitation Therapy for the Critically Injured Burn Patient
Status: Enrolling
Updated:  12/31/1969
University of North Carolina at Chapel Hill
mi
from
Chapel Hill, NC
Early Mobility for the Critically Injured Burn Patient
Early ICU Standardized Rehabilitation Therapy for the Critically Injured Burn Patient
Status: Enrolling
Updated: 12/31/1969
University of North Carolina at Chapel Hill
mi
from
Chapel Hill, NC
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Early Mobility for the Critically Injured Burn Patient
Early ICU Standardized Rehabilitation Therapy for the Critically Injured Burn Patient
Status: Enrolling
Updated:  12/31/1969
Wake Forest University Baptist Medical Center
mi
from
Winston-Salem, NC
Early Mobility for the Critically Injured Burn Patient
Early ICU Standardized Rehabilitation Therapy for the Critically Injured Burn Patient
Status: Enrolling
Updated: 12/31/1969
Wake Forest University Baptist Medical Center
mi
from
Winston-Salem, NC
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Early Mobility for the Critically Injured Burn Patient
Early ICU Standardized Rehabilitation Therapy for the Critically Injured Burn Patient
Status: Enrolling
Updated:  12/31/1969
Washington University
mi
from
Saint Louis, MO
Early Mobility for the Critically Injured Burn Patient
Early ICU Standardized Rehabilitation Therapy for the Critically Injured Burn Patient
Status: Enrolling
Updated: 12/31/1969
Washington University
mi
from
Saint Louis, MO
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Remote Device Interrogation In The Emergency Department
Remote Device Interrogation In The Emergency Department
Status: Enrolling
Updated:  12/31/1969
Genesis Healthcare System
mi
from
Zanesville, OH
Remote Device Interrogation In The Emergency Department
Remote Device Interrogation In The Emergency Department
Status: Enrolling
Updated: 12/31/1969
Genesis Healthcare System
mi
from
Zanesville, OH
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Validation of Lower Body Negative Pressure (LBNP) Model of Human Hemorrhage in Trauma Patients
Validation of LBNP Model of Human Hemorrhage in Trauma Patients
Status: Enrolling
Updated:  12/31/1969
Children's Hospital Colorado
mi
from
Aurora, CO
Validation of Lower Body Negative Pressure (LBNP) Model of Human Hemorrhage in Trauma Patients
Validation of LBNP Model of Human Hemorrhage in Trauma Patients
Status: Enrolling
Updated: 12/31/1969
Children's Hospital Colorado
mi
from
Aurora, CO
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Validation of Lower Body Negative Pressure (LBNP) Model of Human Hemorrhage in Trauma Patients
Validation of LBNP Model of Human Hemorrhage in Trauma Patients
Status: Enrolling
Updated:  12/31/1969
Denver Health Medical Center
mi
from
Denver, CO
Validation of Lower Body Negative Pressure (LBNP) Model of Human Hemorrhage in Trauma Patients
Validation of LBNP Model of Human Hemorrhage in Trauma Patients
Status: Enrolling
Updated: 12/31/1969
Denver Health Medical Center
mi
from
Denver, CO
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Validation of Lower Body Negative Pressure (LBNP) Model of Human Hemorrhage in Trauma Patients
Validation of LBNP Model of Human Hemorrhage in Trauma Patients
Status: Enrolling
Updated:  12/31/1969
San Antonio Military Medical Center
mi
from
San Antonio, TX
Validation of Lower Body Negative Pressure (LBNP) Model of Human Hemorrhage in Trauma Patients
Validation of LBNP Model of Human Hemorrhage in Trauma Patients
Status: Enrolling
Updated: 12/31/1969
San Antonio Military Medical Center
mi
from
San Antonio, TX
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Remotely Deployed TBI Study
Remotely Deployed Training for Cognitive Impairment Associated With TBI
Status: Enrolling
Updated:  12/31/1969
VA Northern California Health Care System
mi
from
Martinez, CA
Remotely Deployed TBI Study
Remotely Deployed Training for Cognitive Impairment Associated With TBI
Status: Enrolling
Updated: 12/31/1969
VA Northern California Health Care System
mi
from
Martinez, CA
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Remotely Deployed TBI Study
Remotely Deployed Training for Cognitive Impairment Associated With TBI
Status: Enrolling
Updated:  12/31/1969
San Francisco VA Medical Center
mi
from
San Francisco, CA
Remotely Deployed TBI Study
Remotely Deployed Training for Cognitive Impairment Associated With TBI
Status: Enrolling
Updated: 12/31/1969
San Francisco VA Medical Center
mi
from
San Francisco, CA
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Targeting Platelet-Leukocyte Aggregates in Pneumonia With Ticagrelor
XANTHIPPE: Examining the Effect of Ticagrelor on Platelet Activation, Platelet-Leukocyte Aggregates, and Acute Lung Injury in Pneumonia
Status: Enrolling
Updated:  12/31/1969
University of Kentucky Hospitals
mi
from
Lexington, KY
Targeting Platelet-Leukocyte Aggregates in Pneumonia With Ticagrelor
XANTHIPPE: Examining the Effect of Ticagrelor on Platelet Activation, Platelet-Leukocyte Aggregates, and Acute Lung Injury in Pneumonia
Status: Enrolling
Updated: 12/31/1969
University of Kentucky Hospitals
mi
from
Lexington, KY
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Targeting Platelet-Leukocyte Aggregates in Pneumonia With Ticagrelor
XANTHIPPE: Examining the Effect of Ticagrelor on Platelet Activation, Platelet-Leukocyte Aggregates, and Acute Lung Injury in Pneumonia
Status: Enrolling
Updated:  12/31/1969
University of Kentucky Hospital
mi
from
Lexington, KY
Targeting Platelet-Leukocyte Aggregates in Pneumonia With Ticagrelor
XANTHIPPE: Examining the Effect of Ticagrelor on Platelet Activation, Platelet-Leukocyte Aggregates, and Acute Lung Injury in Pneumonia
Status: Enrolling
Updated: 12/31/1969
University of Kentucky Hospital
mi
from
Lexington, KY
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Virtual Walking for Neuropathic Pain in Spinal Cord Injury
Virtual Walking for Reducing Spinal Cord Injury-Related Neuropathic Pain
Status: Enrolling
Updated:  12/31/1969
Spain REhabilitation Center
mi
from
Birmingham, AL
Virtual Walking for Neuropathic Pain in Spinal Cord Injury
Virtual Walking for Reducing Spinal Cord Injury-Related Neuropathic Pain
Status: Enrolling
Updated: 12/31/1969
Spain REhabilitation Center
mi
from
Birmingham, AL
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Clinical Characteristics of Dementias That Occur Remotely After Traumatic Brain Injury in Retired Military Personnel
Endophenotypes of Dementia Associated With Traumatic Brain Injury in Retired Military Personnel
Status: Enrolling
Updated:  12/31/1969
California Veterans Home-Yountville
mi
from
Yountville, CA
Clinical Characteristics of Dementias That Occur Remotely After Traumatic Brain Injury in Retired Military Personnel
Endophenotypes of Dementia Associated With Traumatic Brain Injury in Retired Military Personnel
Status: Enrolling
Updated: 12/31/1969
California Veterans Home-Yountville
mi
from
Yountville, CA
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Clinical Characteristics of Dementias That Occur Remotely After Traumatic Brain Injury in Retired Military Personnel
Endophenotypes of Dementia Associated With Traumatic Brain Injury in Retired Military Personnel
Status: Enrolling
Updated:  12/31/1969
Armed Forces Retirement Home
mi
from
Washington,
Clinical Characteristics of Dementias That Occur Remotely After Traumatic Brain Injury in Retired Military Personnel
Endophenotypes of Dementia Associated With Traumatic Brain Injury in Retired Military Personnel
Status: Enrolling
Updated: 12/31/1969
Armed Forces Retirement Home
mi
from
Washington,
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Children With Hemiparesis Arm and Hand Movement Project (CHAMP Study)
A Multisite Trial of Pediatric Constraint-Induced Movement Therapy
Status: Enrolling
Updated:  12/31/1969
Virginia Tech Carilion Research Institute
mi
from
Roanoke, VA
Children With Hemiparesis Arm and Hand Movement Project (CHAMP Study)
A Multisite Trial of Pediatric Constraint-Induced Movement Therapy
Status: Enrolling
Updated: 12/31/1969
Virginia Tech Carilion Research Institute
mi
from
Roanoke, VA
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Upper Extremity Surgery in Spinal Cord Injury
Study of the Surgical Treatment of Cervical Spinal Cord Injuries With Nerve Transfers to Restore Upper Extremity and Hand Function
Status: Enrolling
Updated:  12/31/1969
Washington University Division of Plastic Surgery
mi
from
Saint Louis, MO
Upper Extremity Surgery in Spinal Cord Injury
Study of the Surgical Treatment of Cervical Spinal Cord Injuries With Nerve Transfers to Restore Upper Extremity and Hand Function
Status: Enrolling
Updated: 12/31/1969
Washington University Division of Plastic Surgery
mi
from
Saint Louis, MO
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Tamsulosin for Urolithiasis in the Emergency Dept
Study of Tamsulosin for Urolithiasis in the Emergency Department
Status: Enrolling
Updated:  12/31/1969
The George Washington University Medical Center
mi
from
Washington,
Tamsulosin for Urolithiasis in the Emergency Dept
Study of Tamsulosin for Urolithiasis in the Emergency Department
Status: Enrolling
Updated: 12/31/1969
The George Washington University Medical Center
mi
from
Washington,
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Tamsulosin for Urolithiasis in the Emergency Dept
Study of Tamsulosin for Urolithiasis in the Emergency Department
Status: Enrolling
Updated:  12/31/1969
University of Pittsburgh
mi
from
Pittsburgh, PA
Tamsulosin for Urolithiasis in the Emergency Dept
Study of Tamsulosin for Urolithiasis in the Emergency Department
Status: Enrolling
Updated: 12/31/1969
University of Pittsburgh
mi
from
Pittsburgh, PA
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Tamsulosin for Urolithiasis in the Emergency Dept
Study of Tamsulosin for Urolithiasis in the Emergency Department
Status: Enrolling
Updated:  12/31/1969
University of Alabama at Birmingham
mi
from
Birmingham, AL
Tamsulosin for Urolithiasis in the Emergency Dept
Study of Tamsulosin for Urolithiasis in the Emergency Department
Status: Enrolling
Updated: 12/31/1969
University of Alabama at Birmingham
mi
from
Birmingham, AL
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Tamsulosin for Urolithiasis in the Emergency Dept
Study of Tamsulosin for Urolithiasis in the Emergency Department
Status: Enrolling
Updated:  12/31/1969
Thomas Jefferson University
mi
from
Philadelphia, PA
Tamsulosin for Urolithiasis in the Emergency Dept
Study of Tamsulosin for Urolithiasis in the Emergency Department
Status: Enrolling
Updated: 12/31/1969
Thomas Jefferson University
mi
from
Philadelphia, PA
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DHA For The Treatment of Pediatric Concussion Related to Sports Injury
Docosahexaenoic Acid (DHA) For The Treatment of Pediatric Concussion Related to Sports Injury
Status: Enrolling
Updated:  12/31/1969
Sports Medicine at Texas Scottish Rite Hospital for Children
mi
from
Plano, TX
DHA For The Treatment of Pediatric Concussion Related to Sports Injury
Docosahexaenoic Acid (DHA) For The Treatment of Pediatric Concussion Related to Sports Injury
Status: Enrolling
Updated: 12/31/1969
Sports Medicine at Texas Scottish Rite Hospital for Children
mi
from
Plano, TX
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Stem Cell Fistula Plug in Perianal Crohn's Disease
A Phase 1 Study of Autologous Mesenchymal Stromal Cell Coated Fistula Plug in Patients With Fistulizing Crohn's Disease.
Status: Enrolling
Updated:  12/31/1969
The Mayo Clinic
mi
from
Rochester, MN
Stem Cell Fistula Plug in Perianal Crohn's Disease
A Phase 1 Study of Autologous Mesenchymal Stromal Cell Coated Fistula Plug in Patients With Fistulizing Crohn's Disease.
Status: Enrolling
Updated: 12/31/1969
The Mayo Clinic
mi
from
Rochester, MN
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Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Mobile, AL
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Mobile, AL
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Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Phoenix, AZ
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Idaho Falls, ID
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Idaho Falls, ID
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Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Indianapolis, IN
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Indianapolis, IN
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Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Hazard, KY
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Hazard, KY
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Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Jackson, MS
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Jackson, MS
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Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Butte, MT
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Butte, MT
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Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Englewood, NJ
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Englewood, NJ
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Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Durham, NC
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Durham, NC
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Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Oklahoma City, OK
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Oklahoma City, OK
Click here to add this to my saved trials
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Rapid City, SD
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Rapid City, SD
Click here to add this to my saved trials
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
2 of 2
mi
from
Houston, TX
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
2 of 2
mi
from
Houston, TX
Click here to add this to my saved trials
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Murray, UT
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Murray, UT
Click here to add this to my saved trials
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Harper Hospital - Wayne State University School of Medicine
mi
from
Detroit, MI
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Harper Hospital - Wayne State University School of Medicine
mi
from
Detroit, MI
Click here to add this to my saved trials
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Washington University in St. Louis
mi
from
Saint Louis, MO
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Washington University in St. Louis
mi
from
Saint Louis, MO
Click here to add this to my saved trials
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Memorial Sloan Kettering Cancer Center
mi
from
New York, NY
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Memorial Sloan Kettering Cancer Center
mi
from
New York, NY
Click here to add this to my saved trials
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Columbus, OH
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Columbus, OH
Click here to add this to my saved trials
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Atlanta, GA
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Atlanta, GA
Click here to add this to my saved trials
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Louisville, KY
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Louisville, KY
Click here to add this to my saved trials
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Detroit Receiving Hospital
mi
from
Detroit, MI
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Detroit Receiving Hospital
mi
from
Detroit, MI
Click here to add this to my saved trials
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Sinai-Grace Hospital
mi
from
Detroit, MI
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Sinai-Grace Hospital
mi
from
Detroit, MI
Click here to add this to my saved trials
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Philadelphia, PA
Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Philadelphia, PA
Click here to add this to my saved trials