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

An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Metrolina Nephrology Associates, PA
mi
from
Charlotte, NC
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Metrolina Nephrology Associates, PA
mi
from
Charlotte, NC
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
ECU Department of Nephrology and Hypertension
mi
from
Greenville, NC
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
ECU Department of Nephrology and Hypertension
mi
from
Greenville, NC
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Sanford Research/USD-Fargo
mi
from
Fargo, ND
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Sanford Research/USD-Fargo
mi
from
Fargo, ND
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
University of Cincinnati Physicians Company, LLC
mi
from
Cincinnati, OH
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
University of Cincinnati Physicians Company, LLC
mi
from
Cincinnati, OH
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Cleveland Clinic Foundation
mi
from
Cleveland, OH
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Cleveland Clinic Foundation
mi
from
Cleveland, OH
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Ohio State University
mi
from
Columbus, OH
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Ohio State University
mi
from
Columbus, OH
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Toledo Hospital
mi
from
Toledo, OH
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Toledo Hospital
mi
from
Toledo, OH
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Kaiser Permanente Northwest
mi
from
Milwaukie, OR
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Kaiser Permanente Northwest
mi
from
Milwaukie, OR
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Northwest Renal Clinic, Inc.
mi
from
Portland, OR
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Northwest Renal Clinic, Inc.
mi
from
Portland, OR
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Temple University School of Medicine
mi
from
Philadelphia, PA
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Temple University School of Medicine
mi
from
Philadelphia, PA
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Delaware Valley Nephrology and Hypertension Associates, PC
mi
from
Philadelphia, PA
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Delaware Valley Nephrology and Hypertension Associates, PC
mi
from
Philadelphia, PA
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Penn Medicine, Perelman Center for Advanced Medicine
mi
from
Philadelphia, PA
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Penn Medicine, Perelman Center for Advanced Medicine
mi
from
Philadelphia, PA
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
SC Nephrology & Hypertension Center, Inc.
mi
from
Orangeberg, SC
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
SC Nephrology & Hypertension Center, Inc.
mi
from
Orangeberg, SC
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Erlanger Hospital Pharmacy
mi
from
Chattanooga, TN
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Erlanger Hospital Pharmacy
mi
from
Chattanooga, TN
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Nephrology Associates, PC
mi
from
Nashville, TN
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Nephrology Associates, PC
mi
from
Nashville, TN
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Baylor College of Medicine ICTR
mi
from
Houston, TX
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Baylor College of Medicine ICTR
mi
from
Houston, TX
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Fletcher Allen Health Care Renal Service
mi
from
Burlington, VT
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Fletcher Allen Health Care Renal Service
mi
from
Burlington, VT
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Sentara Vascular Specialists
mi
from
Norfolk, VA
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Sentara Vascular Specialists
mi
from
Norfolk, VA
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Wenatchee Valley Medical Center
mi
from
Wenatchee, WA
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Wenatchee Valley Medical Center
mi
from
Wenatchee, WA
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
University of Wisconsin
mi
from
Madison, WI
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
University of Wisconsin
mi
from
Madison, WI
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
University of California at San Francisco
mi
from
San Francisco, CA
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
University of California at San Francisco
mi
from
San Francisco, CA
Click here to add this to my saved trials
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated:  11/20/2015
Washington University School of Medicine
mi
from
St. Louis, MO
An Efficacy and Safety Study of SRM003 in the Treatment of Subjects Undergoing Creation of an Arteriovenous Fistula to Facilitate Hemodialysis Access
A Phase 2, Single-blind, Randomized, Controlled, Multi-center Study to Evaluate the Efficacy and Safety of SRM003 (Vascugel®) in Improving the Rate of Arteriovenous Fistula Maturation and Use in Subjects Undergoing Surgery for Creation of an Arteriovenous Fistula for Hemodialysis Access
Status: Enrolling
Updated: 11/20/2015
Washington University School of Medicine
mi
from
St. Louis, MO
Click here to add this to my saved trials
Quetiapine for Delirium Prophylaxis in High-risk Critically Ill Patients
Quetiapine for Delirium Prophylaxis in High-risk Critically Ill Patients
Status: Enrolling
Updated:  11/21/2015
University of Tennessee Medical Center
mi
from
Knoxville, TN
Quetiapine for Delirium Prophylaxis in High-risk Critically Ill Patients
Quetiapine for Delirium Prophylaxis in High-risk Critically Ill Patients
Status: Enrolling
Updated: 11/21/2015
University of Tennessee Medical Center
mi
from
Knoxville, TN
Click here to add this to my saved trials
Multidisciplinary Approach to Reduce Injury and Substance Abuse
Multidisciplinary Approach to Reduce Injury and Substance Abuse
Status: Enrolling
Updated:  11/23/2015
University Medical Center Brackenridge
mi
from
Austin, TX
Multidisciplinary Approach to Reduce Injury and Substance Abuse
Multidisciplinary Approach to Reduce Injury and Substance Abuse
Status: Enrolling
Updated: 11/23/2015
University Medical Center Brackenridge
mi
from
Austin, TX
Click here to add this to my saved trials
A Randomized, Double-Blind Study of Placebo vs. Ketamine For Use During Dressing Changes in Critically Ill Burn Patients
A Randomized, Double-Blind Study of Placebo vs. Ketamine For Use During Dressing Changes in Critically Ill Burn Patients
Status: Enrolling
Updated:  11/24/2015
University of Colorado
mi
from
Aurora, CO
A Randomized, Double-Blind Study of Placebo vs. Ketamine For Use During Dressing Changes in Critically Ill Burn Patients
A Randomized, Double-Blind Study of Placebo vs. Ketamine For Use During Dressing Changes in Critically Ill Burn Patients
Status: Enrolling
Updated: 11/24/2015
University of Colorado
mi
from
Aurora, CO
Click here to add this to my saved trials
Comparison of Techniques for Assessing Cardiac Output and Preload in Critically Ill Pediatric Patients
Comparison of Techniques for Assessing Cardiac Output and Preload in Critically Ill Patients
Status: Enrolling
Updated:  11/25/2015
University of Rochester
mi
from
Rochester, NY
Comparison of Techniques for Assessing Cardiac Output and Preload in Critically Ill Pediatric Patients
Comparison of Techniques for Assessing Cardiac Output and Preload in Critically Ill Patients
Status: Enrolling
Updated: 11/25/2015
University of Rochester
mi
from
Rochester, NY
Click here to add this to my saved trials
A Relative Bioavailability Study of Valcyte (Valganciclovir) in Lung Transplant Recipients With or Without Cystic Fibrosis.
Relative Bioavailability Study of Ganciclovir From the Pro-drug, Valganciclovir, in Lung Transplant Recipients With or Without Cystic Fibrosis
Status: Enrolling
Updated:  11/26/2015
Clinical Research Facility
mi
from
Los Angeles, CA
A Relative Bioavailability Study of Valcyte (Valganciclovir) in Lung Transplant Recipients With or Without Cystic Fibrosis.
Relative Bioavailability Study of Ganciclovir From the Pro-drug, Valganciclovir, in Lung Transplant Recipients With or Without Cystic Fibrosis
Status: Enrolling
Updated: 11/26/2015
Clinical Research Facility
mi
from
Los Angeles, CA
Click here to add this to my saved trials
A Relative Bioavailability Study of Valcyte (Valganciclovir) in Lung Transplant Recipients With or Without Cystic Fibrosis.
Relative Bioavailability Study of Ganciclovir From the Pro-drug, Valganciclovir, in Lung Transplant Recipients With or Without Cystic Fibrosis
Status: Enrolling
Updated:  11/26/2015
Clinical Research Facility
mi
from
Denver, CO
A Relative Bioavailability Study of Valcyte (Valganciclovir) in Lung Transplant Recipients With or Without Cystic Fibrosis.
Relative Bioavailability Study of Ganciclovir From the Pro-drug, Valganciclovir, in Lung Transplant Recipients With or Without Cystic Fibrosis
Status: Enrolling
Updated: 11/26/2015
Clinical Research Facility
mi
from
Denver, CO
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A Relative Bioavailability Study of Valcyte (Valganciclovir) in Lung Transplant Recipients With or Without Cystic Fibrosis.
Relative Bioavailability Study of Ganciclovir From the Pro-drug, Valganciclovir, in Lung Transplant Recipients With or Without Cystic Fibrosis
Status: Enrolling
Updated:  11/26/2015
Clinical Research Facility
mi
from
Durham, NC
A Relative Bioavailability Study of Valcyte (Valganciclovir) in Lung Transplant Recipients With or Without Cystic Fibrosis.
Relative Bioavailability Study of Ganciclovir From the Pro-drug, Valganciclovir, in Lung Transplant Recipients With or Without Cystic Fibrosis
Status: Enrolling
Updated: 11/26/2015
Clinical Research Facility
mi
from
Durham, NC
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A Relative Bioavailability Study of Valcyte (Valganciclovir) in Lung Transplant Recipients With or Without Cystic Fibrosis.
Relative Bioavailability Study of Ganciclovir From the Pro-drug, Valganciclovir, in Lung Transplant Recipients With or Without Cystic Fibrosis
Status: Enrolling
Updated:  11/26/2015
Clinical Research Facility
mi
from
Cleveland, OH
A Relative Bioavailability Study of Valcyte (Valganciclovir) in Lung Transplant Recipients With or Without Cystic Fibrosis.
Relative Bioavailability Study of Ganciclovir From the Pro-drug, Valganciclovir, in Lung Transplant Recipients With or Without Cystic Fibrosis
Status: Enrolling
Updated: 11/26/2015
Clinical Research Facility
mi
from
Cleveland, OH
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A Relative Bioavailability Study of Valcyte (Valganciclovir) in Lung Transplant Recipients With or Without Cystic Fibrosis.
Relative Bioavailability Study of Ganciclovir From the Pro-drug, Valganciclovir, in Lung Transplant Recipients With or Without Cystic Fibrosis
Status: Enrolling
Updated:  11/26/2015
Clinical Research Facility
mi
from
Pittsburgh, PA
A Relative Bioavailability Study of Valcyte (Valganciclovir) in Lung Transplant Recipients With or Without Cystic Fibrosis.
Relative Bioavailability Study of Ganciclovir From the Pro-drug, Valganciclovir, in Lung Transplant Recipients With or Without Cystic Fibrosis
Status: Enrolling
Updated: 11/26/2015
Clinical Research Facility
mi
from
Pittsburgh, PA
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Hypothermia in Acute Stroke With Thrombolysis Imaging Evaluation of Revascularization
An Ancillary Imaging Study to the Intravascular Cooling in the Treatment of Stroke 2 (ICTuS 2) Trial, an NIH-funded Project on the Safety and Efficacy of Hypothermia Combined With Thrombolysis
Status: Enrolling
Updated:  11/30/2015
Cedars-Sinai Medical Center
mi
from
Los Angeles, CA
Hypothermia in Acute Stroke With Thrombolysis Imaging Evaluation of Revascularization
An Ancillary Imaging Study to the Intravascular Cooling in the Treatment of Stroke 2 (ICTuS 2) Trial, an NIH-funded Project on the Safety and Efficacy of Hypothermia Combined With Thrombolysis
Status: Enrolling
Updated: 11/30/2015
Cedars-Sinai Medical Center
mi
from
Los Angeles, CA
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Hypothermia in Acute Stroke With Thrombolysis Imaging Evaluation of Revascularization
An Ancillary Imaging Study to the Intravascular Cooling in the Treatment of Stroke 2 (ICTuS 2) Trial, an NIH-funded Project on the Safety and Efficacy of Hypothermia Combined With Thrombolysis
Status: Enrolling
Updated:  11/30/2015
Intercoastal Medical Group
mi
from
Sarasota, FL
Hypothermia in Acute Stroke With Thrombolysis Imaging Evaluation of Revascularization
An Ancillary Imaging Study to the Intravascular Cooling in the Treatment of Stroke 2 (ICTuS 2) Trial, an NIH-funded Project on the Safety and Efficacy of Hypothermia Combined With Thrombolysis
Status: Enrolling
Updated: 11/30/2015
Intercoastal Medical Group
mi
from
Sarasota, FL
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Hypothermia in Acute Stroke With Thrombolysis Imaging Evaluation of Revascularization
An Ancillary Imaging Study to the Intravascular Cooling in the Treatment of Stroke 2 (ICTuS 2) Trial, an NIH-funded Project on the Safety and Efficacy of Hypothermia Combined With Thrombolysis
Status: Enrolling
Updated:  11/30/2015
University of California, San Diego
mi
from
San Diego, CA
Hypothermia in Acute Stroke With Thrombolysis Imaging Evaluation of Revascularization
An Ancillary Imaging Study to the Intravascular Cooling in the Treatment of Stroke 2 (ICTuS 2) Trial, an NIH-funded Project on the Safety and Efficacy of Hypothermia Combined With Thrombolysis
Status: Enrolling
Updated: 11/30/2015
University of California, San Diego
mi
from
San Diego, CA
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Advanced MRI Applications for Mild Traumatic Brain Injury
Advanced MRI Applications for Mild Traumatic Brain Injury
Status: Enrolling
Updated:  11/30/2015
Hospital for Special Surgery
mi
from
New York, NY
Advanced MRI Applications for Mild Traumatic Brain Injury
Advanced MRI Applications for Mild Traumatic Brain Injury
Status: Enrolling
Updated: 11/30/2015
Hospital for Special Surgery
mi
from
New York, NY
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Advanced MRI Applications for Mild Traumatic Brain Injury - UCSF
Advanced MRI Applications for Mild Traumatic Brain Injury - UCSF
Status: Enrolling
Updated:  11/30/2015
University of California at San Francisco (UCSF)
mi
from
San Francisco, CA
Advanced MRI Applications for Mild Traumatic Brain Injury - UCSF
Advanced MRI Applications for Mild Traumatic Brain Injury - UCSF
Status: Enrolling
Updated: 11/30/2015
University of California at San Francisco (UCSF)
mi
from
San Francisco, CA
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TBI MR Study 3 Houston Methodist
Advanced MRI Applications for Mild Traumatic Brain Injury - Study 3
Status: Enrolling
Updated:  11/30/2015
Houston Methodist Neurological Institute
mi
from
Houston, TX
TBI MR Study 3 Houston Methodist
Advanced MRI Applications for Mild Traumatic Brain Injury - Study 3
Status: Enrolling
Updated: 11/30/2015
Houston Methodist Neurological Institute
mi
from
Houston, TX
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Health Interventions for Survivors and Primary Support Persons of Spinal Cord Injury
Caregiver Intervention for Caregivers of SCI Patients
Status: Enrolling
Updated:  11/30/2015
University of Miami
mi
from
Miami, FL
Health Interventions for Survivors and Primary Support Persons of Spinal Cord Injury
Caregiver Intervention for Caregivers of SCI Patients
Status: Enrolling
Updated: 11/30/2015
University of Miami
mi
from
Miami, FL
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Health Interventions for Survivors and Primary Support Persons of Spinal Cord Injury
Caregiver Intervention for Caregivers of SCI Patients
Status: Enrolling
Updated:  11/30/2015
University of Pittsburgh (UCSUR)
mi
from
Pittsburgh, PA
Health Interventions for Survivors and Primary Support Persons of Spinal Cord Injury
Caregiver Intervention for Caregivers of SCI Patients
Status: Enrolling
Updated: 11/30/2015
University of Pittsburgh (UCSUR)
mi
from
Pittsburgh, PA
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A Randomized Trial of GM-CSF in Patients With ALI/ARDS
A Randomized Trial of GM-CSF in Patients With ALI/ARDS
Status: Enrolling
Updated:  11/30/2015
University of Colorado Health Sciences Center
mi
from
Denver, CO
A Randomized Trial of GM-CSF in Patients With ALI/ARDS
A Randomized Trial of GM-CSF in Patients With ALI/ARDS
Status: Enrolling
Updated: 11/30/2015
University of Colorado Health Sciences Center
mi
from
Denver, CO
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A Randomized Trial of GM-CSF in Patients With ALI/ARDS
A Randomized Trial of GM-CSF in Patients With ALI/ARDS
Status: Enrolling
Updated:  11/30/2015
Emory University
mi
from
Atlanta, GA
A Randomized Trial of GM-CSF in Patients With ALI/ARDS
A Randomized Trial of GM-CSF in Patients With ALI/ARDS
Status: Enrolling
Updated: 11/30/2015
Emory University
mi
from
Atlanta, GA
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A Randomized Trial of GM-CSF in Patients With ALI/ARDS
A Randomized Trial of GM-CSF in Patients With ALI/ARDS
Status: Enrolling
Updated:  11/30/2015
University of Michigan
mi
from
Ann Arbor, MI
A Randomized Trial of GM-CSF in Patients With ALI/ARDS
A Randomized Trial of GM-CSF in Patients With ALI/ARDS
Status: Enrolling
Updated: 11/30/2015
University of Michigan
mi
from
Ann Arbor, MI
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Pharmacokinetics of Daptomycin in Critically Ill Patients Receiving Continuous Venovenous Hemodialysis (CVVHD)
Pharmacokinetics of Daptomycin in Critically Ill Patients Receiving Continuous Venovenous Hemodialysis (CVVHD)
Status: Enrolling
Updated:  12/1/2015
University of Michigan University Hospital
mi
from
Ann Arbor, MI
Pharmacokinetics of Daptomycin in Critically Ill Patients Receiving Continuous Venovenous Hemodialysis (CVVHD)
Pharmacokinetics of Daptomycin in Critically Ill Patients Receiving Continuous Venovenous Hemodialysis (CVVHD)
Status: Enrolling
Updated: 12/1/2015
University of Michigan University Hospital
mi
from
Ann Arbor, MI
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Treatment Study for Non-Suicidal Self-Injury
Exploring Two Emotion-Focused Treatment Modules in Non-Suicidal Self-Injury
Status: Enrolling
Updated:  12/2/2015
Center for Anxiety and Related Disorders, Boston University
mi
from
Boston, MA
Treatment Study for Non-Suicidal Self-Injury
Exploring Two Emotion-Focused Treatment Modules in Non-Suicidal Self-Injury
Status: Enrolling
Updated: 12/2/2015
Center for Anxiety and Related Disorders, Boston University
mi
from
Boston, MA
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Continuous Noninvasive Method for Estimating and Predicting Maternal and Fetal Hemodynamic Changes During Regional Anesthesia
A Continuous, Noninvasive Method for Estimating and Predicting Maternal and Fetal Hemodynamic Changes During Regional Anesthesia
Status: Enrolling
Updated:  12/3/2015
Children's Hospital Colorado
mi
from
Aurora, CO
Continuous Noninvasive Method for Estimating and Predicting Maternal and Fetal Hemodynamic Changes During Regional Anesthesia
A Continuous, Noninvasive Method for Estimating and Predicting Maternal and Fetal Hemodynamic Changes During Regional Anesthesia
Status: Enrolling
Updated: 12/3/2015
Children's Hospital Colorado
mi
from
Aurora, CO
Click here to add this to my saved trials
Continuous Noninvasive Method for Estimating and Predicting Maternal and Fetal Hemodynamic Changes During Regional Anesthesia
A Continuous, Noninvasive Method for Estimating and Predicting Maternal and Fetal Hemodynamic Changes During Regional Anesthesia
Status: Enrolling
Updated:  12/3/2015
University of Colorado Hospital
mi
from
Aurora, CO
Continuous Noninvasive Method for Estimating and Predicting Maternal and Fetal Hemodynamic Changes During Regional Anesthesia
A Continuous, Noninvasive Method for Estimating and Predicting Maternal and Fetal Hemodynamic Changes During Regional Anesthesia
Status: Enrolling
Updated: 12/3/2015
University of Colorado Hospital
mi
from
Aurora, CO
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Strategies To Prevent Pneumonia 2 (SToPP2)
Oral Care Intervention in Mechanically Ventilated Adults
Status: Enrolling
Updated:  12/4/2015
Virginia Commonwealth University
mi
from
Richmond, VA
Strategies To Prevent Pneumonia 2 (SToPP2)
Oral Care Intervention in Mechanically Ventilated Adults
Status: Enrolling
Updated: 12/4/2015
Virginia Commonwealth University
mi
from
Richmond, VA
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Acetaminophen to Prevent Ischemic Oxidative Reperfusion Injury During Percutaneous Coronary Intervention for Acute Myocardial Infarction
Acetaminophen to Prevent Ischemic Oxidative Reperfusion Injury During Percutaneous Coronary Intervention for Acute Myocardial Infarction
Status: Enrolling
Updated:  12/4/2015
Vanderbilt University Medical Center
mi
from
Nashville, TN
Acetaminophen to Prevent Ischemic Oxidative Reperfusion Injury During Percutaneous Coronary Intervention for Acute Myocardial Infarction
Acetaminophen to Prevent Ischemic Oxidative Reperfusion Injury During Percutaneous Coronary Intervention for Acute Myocardial Infarction
Status: Enrolling
Updated: 12/4/2015
Vanderbilt University Medical Center
mi
from
Nashville, TN
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Clinical Evaluation of the Ultrasound-Guided Retroclavicular Brachial Plexus Block
Clinical Evaluation of the Ultrasound-Guided Retroclavicular Brachial Plexus Block
Status: Enrolling
Updated:  12/4/2015
Brigham and Women's Hosp
mi
from
Boston, MA
Clinical Evaluation of the Ultrasound-Guided Retroclavicular Brachial Plexus Block
Clinical Evaluation of the Ultrasound-Guided Retroclavicular Brachial Plexus Block
Status: Enrolling
Updated: 12/4/2015
Brigham and Women's Hosp
mi
from
Boston, MA
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Topiramate Treatment of Hazardous and Harmful Alcohol Use in Veterans With TBI
Status: Enrolling
Updated:  12/4/2015
San Francisco VA Medical Center
mi
from
San Francisco, CA
Topiramate Treatment of Hazardous and Harmful Alcohol Use in Veterans With TBI
Status: Enrolling
Updated: 12/4/2015
San Francisco VA Medical Center
mi
from
San Francisco, CA
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