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.

Zip code

Condition


Search Radius:25 Miles
  • 5
  • 10
  • 15
  • 20
  • 25
  • 30
  • 40
  • 50
  • 100
  • 500
  • All

We've found
6,666
archived clinical trials in
Hospital

Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated:  12/31/1969
Arlington Family Research Center
mi
from
Arlington, TX
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated: 12/31/1969
Arlington Family Research Center
mi
from
Arlington, TX
Click here to add this to my saved trials
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated:  12/31/1969
Utah Valley Pediatrics
mi
from
Orem, UT
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated: 12/31/1969
Utah Valley Pediatrics
mi
from
Orem, UT
Click here to add this to my saved trials
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated:  12/31/1969
J. Lewis Research Inc./Foothill Family Clininc
mi
from
Salt Lake City, UT
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated: 12/31/1969
J. Lewis Research Inc./Foothill Family Clininc
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated:  12/31/1969
J. Lewis Research - FirstMed East
mi
from
Salt Lake City, UT
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated: 12/31/1969
J. Lewis Research - FirstMed East
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated:  12/31/1969
J. Lewis Research, Inc. / Foothill Family Clinic South
mi
from
Salt Lake City, UT
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated: 12/31/1969
J. Lewis Research, Inc. / Foothill Family Clinic South
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated:  12/31/1969
Legacy Point Family Medicine
mi
from
West Point, UT
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated: 12/31/1969
Legacy Point Family Medicine
mi
from
West Point, UT
Click here to add this to my saved trials
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated:  12/31/1969
Pediatric Research of Charlottesville, LLC
mi
from
Charlottesville, VA
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated: 12/31/1969
Pediatric Research of Charlottesville, LLC
mi
from
Charlottesville, VA
Click here to add this to my saved trials
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated:  12/31/1969
Score Physician Alliance, LLC
mi
from
Saint Petersburg, FL
Safety Study of Flector Patch in Children With Minor Soft Tissue Injuries
An Open-label, Prospective, Uncontrolled Study of the Safety and Local Tolerability of the Diclofenac Epolamine Patch (Flector Patch) in Pediatric Patients With Minor Soft Tissue Injuries
Status: Enrolling
Updated: 12/31/1969
Score Physician Alliance, LLC
mi
from
Saint Petersburg, FL
Click here to add this to my saved trials
C1INH Inhibitor Preoperative and Post Kidney Transplant to Prevent DGF & IRI
Assessing Safety and Efficacy of Preoperative and Post-Transplant C1 Inhibitor (Berinert®) vs. Placebo in Recipients of a Renal Allograft From Deceased High Risk Donors and Its Impact on DGF and IRI
Status: Enrolling
Updated:  12/31/1969
Cedars-Sinai Medical Center
mi
from
Los Angeles, CA
C1INH Inhibitor Preoperative and Post Kidney Transplant to Prevent DGF & IRI
Assessing Safety and Efficacy of Preoperative and Post-Transplant C1 Inhibitor (Berinert®) vs. Placebo in Recipients of a Renal Allograft From Deceased High Risk Donors and Its Impact on DGF and IRI
Status: Enrolling
Updated: 12/31/1969
Cedars-Sinai Medical Center
mi
from
Los Angeles, CA
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
Barrow Neurological Institute - St. Joseph's Hospital and Medical Center
mi
from
Phoenix, AZ
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Barrow Neurological Institute - St. Joseph's Hospital and Medical Center
mi
from
Phoenix, AZ
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
USC, Keck School of Medicine
mi
from
Los Angeles, CA
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
USC, Keck School of Medicine
mi
from
Los Angeles, CA
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
University of California, Davis Medical Center
mi
from
Sacramento, CA
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
University of California, Davis Medical Center
mi
from
Sacramento, CA
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
Cooper Neurological Institute
mi
from
Camden, NJ
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Cooper Neurological Institute
mi
from
Camden, NJ
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
Carolina NeuroSurgery and Spine Associates/Carolinas Rehabilitation
mi
from
Charlotte, NC
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Carolina NeuroSurgery and Spine Associates/Carolinas Rehabilitation
mi
from
Charlotte, NC
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
Oregon Health and Science University
mi
from
Portland, OR
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Oregon Health and Science University
mi
from
Portland, OR
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
Vidant Medical Center
mi
from
Greenville, NC
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Vidant Medical Center
mi
from
Greenville, NC
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
Allegheny General Hospital
mi
from
Pittsburgh, PA
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Allegheny General Hospital
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
Barnes-Jewish Hospital at Washington University Medical Center
mi
from
Saint Louis, MO
The INSPIRE Study: Probable Benefit of the Neuro-spinal Scaffold for Treatment of AIS A Thoracic Acute Spinal Cord Injury
The INSPIRE Study: InVivo Study of Probable Benefit of the Neuro-Spinal Scaffold(TM) for Safety and Neurologic Recovery in Subjects With Complete Thoracic AIS A Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Barnes-Jewish Hospital at Washington University Medical Center
mi
from
Saint Louis, MO
Click here to add this to my saved trials
Prevention of Retained-Blood Outcomes With Active Clearance Technology
Prevention of Retained-Blood Outcomes With Active Clearance Technology. ACT Registry
Status: Enrolling
Updated:  12/31/1969
Catholic Medical Center
mi
from
Manchester, NH
Prevention of Retained-Blood Outcomes With Active Clearance Technology
Prevention of Retained-Blood Outcomes With Active Clearance Technology. ACT Registry
Status: Enrolling
Updated: 12/31/1969
Catholic Medical Center
mi
from
Manchester, NH
Click here to add this to my saved trials
Prevention of Retained-Blood Outcomes With Active Clearance Technology
Prevention of Retained-Blood Outcomes With Active Clearance Technology. ACT Registry
Status: Enrolling
Updated:  12/31/1969
Vanderbilt University Medical Center
mi
from
Nashville, TN
Prevention of Retained-Blood Outcomes With Active Clearance Technology
Prevention of Retained-Blood Outcomes With Active Clearance Technology. ACT Registry
Status: Enrolling
Updated: 12/31/1969
Vanderbilt University Medical Center
mi
from
Nashville, TN
Click here to add this to my saved trials
Effect of Recombinant Erythropoietin on Numbers of Circulating Endothelial Progenitor Cells in Subacute TBI
Effect of Administration of Recombinant Erythropoietin on Numbers of Circulating Endothelial Progenitor Cells in Patients With Persistent Symptoms During the Subacute Period After TBI
Status: Enrolling
Updated:  12/31/1969
National Institutes of Health Clinical Center
mi
from
Bethesda, MD
Effect of Recombinant Erythropoietin on Numbers of Circulating Endothelial Progenitor Cells in Subacute TBI
Effect of Administration of Recombinant Erythropoietin on Numbers of Circulating Endothelial Progenitor Cells in Patients With Persistent Symptoms During the Subacute Period After TBI
Status: Enrolling
Updated: 12/31/1969
National Institutes of Health Clinical Center
mi
from
Bethesda, MD
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Maricopa Medical Center
mi
from
Phoenix, AZ
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Maricopa Medical Center
mi
from
Phoenix, AZ
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
University of Colorado at Denver, Teaching
mi
from
Aurora, CO
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
University of Colorado at Denver, Teaching
mi
from
Aurora, CO
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
University of Iowa Hospitals and Clinics
mi
from
Iowa City, IA
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
University of Iowa Hospitals and Clinics
mi
from
Iowa City, IA
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Burnett Burn Center at The University of Kansas Hospital
mi
from
Kansas City, KA
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Burnett Burn Center at The University of Kansas Hospital
mi
from
Kansas City, KA
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
The General Hospital Corporation d/b/a Massachusetts General Hospital
mi
from
Boston, MA
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
The General Hospital Corporation d/b/a Massachusetts General Hospital
mi
from
Boston, MA
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Emergency Medicine Stony Brook University Hospital
mi
from
Stony Brook, NY
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Emergency Medicine Stony Brook University Hospital
mi
from
Stony Brook, NY
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Lehigh Valley Hospital and Health Network
mi
from
Allentown, PA
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Lehigh Valley Hospital and Health Network
mi
from
Allentown, PA
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
University Hospital, Department of Plastic Surgery
mi
from
Gent,
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
University Hospital, Department of Plastic Surgery
mi
from
Gent,
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
University of South Alabama Department of Surgery
mi
from
Mobile, AL
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
University of South Alabama Department of Surgery
mi
from
Mobile, AL
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
MedStar Washington Hospital Center
mi
from
Washington,
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
MedStar Washington Hospital Center
mi
from
Washington,
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
University of Florida- Dept. of Surgery
mi
from
Gainesville, FL
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
University of Florida- Dept. of Surgery
mi
from
Gainesville, FL
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Joseph M. Still Research Foundation, Inc.
mi
from
Augusta, GA
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Joseph M. Still Research Foundation, Inc.
mi
from
Augusta, GA
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Johns Hopkins Bayview Medical Center
mi
from
Baltimore, MD
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Johns Hopkins Bayview Medical Center
mi
from
Baltimore, MD
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
New York-Presbyterian Hospital
mi
from
New York, NY
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
New York-Presbyterian Hospital
mi
from
New York, NY
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Regional Medical Center ,Regional One Health
mi
from
Memphis, TN
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Regional Medical Center ,Regional One Health
mi
from
Memphis, TN
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
University of Texas Medical Branch
mi
from
Galveston, TX
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
University of Texas Medical Branch
mi
from
Galveston, TX
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
University Of Utah Hospital
mi
from
Salt Lake City, UT
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
University Of Utah Hospital
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Harborview Medical Center
mi
from
Seattle, WA
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Harborview Medical Center
mi
from
Seattle, WA
Click here to add this to my saved trials
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated:  12/31/1969
Columbia - St. Mary's
mi
from
Milwaukee, WI
A Study to Evaluate the Efficacy and Safety of NexoBrid in Subjects With Thermal Burns
A Multicenter, Multinational, Randomized, Controlled, Assessor Blinded Study, Performed in Subjects With Thermal Burns, to Evaluate the Efficacy and Safety of NexoBrid Compared to Gel Vehicle and Compared to Standard of Care
Status: Enrolling
Updated: 12/31/1969
Columbia - St. Mary's
mi
from
Milwaukee, WI
Click here to add this to my saved trials
Dopamine Receptor Imaging to Predict Response to Stimulant Therapy in Chronic TBI
Dopamine Receptor Imaging to Predict Response to Stimulant Therapy in Chronic TBI
Status: Enrolling
Updated:  12/31/1969
National Institutes of Health Clinical Center
mi
from
Bethesda, MD
Dopamine Receptor Imaging to Predict Response to Stimulant Therapy in Chronic TBI
Dopamine Receptor Imaging to Predict Response to Stimulant Therapy in Chronic TBI
Status: Enrolling
Updated: 12/31/1969
National Institutes of Health Clinical Center
mi
from
Bethesda, MD
Click here to add this to my saved trials
Efficacy of Nitric Oxide Administration in Attenuating Ischemia/Reperfusion Injury During Neonatal Cardiopulmonary Bypass
Efficacy of Nitric Oxide Administration in Attenuating Ischemia/Reperfusion Injury During Neonatal Cardiopulmonary Bypass.
Status: Enrolling
Updated:  12/31/1969
Advocate Children's Hospital
mi
from
Oak Lawn, IL
Efficacy of Nitric Oxide Administration in Attenuating Ischemia/Reperfusion Injury During Neonatal Cardiopulmonary Bypass
Efficacy of Nitric Oxide Administration in Attenuating Ischemia/Reperfusion Injury During Neonatal Cardiopulmonary Bypass.
Status: Enrolling
Updated: 12/31/1969
Advocate Children's Hospital
mi
from
Oak Lawn, IL
Click here to add this to my saved trials
rTMS to Improve Cognitive Function in TBI
Repetitive Transcranial Magnetic Stimulation to Improve Cognitive Function in TBI
Status: Enrolling
Updated:  12/31/1969
VA Palo Alto Health Care System, Palo Alto, CA
mi
from
Palo Alto, CA
rTMS to Improve Cognitive Function in TBI
Repetitive Transcranial Magnetic Stimulation to Improve Cognitive Function in TBI
Status: Enrolling
Updated: 12/31/1969
VA Palo Alto Health Care System, Palo Alto, CA
mi
from
Palo Alto, CA
Click here to add this to my saved trials
Neuromuscular Mechanisms Underlying Poor Recovery From Whiplash Injuries
Neuromuscular Mechanisms Underlying Poor Recovery From Whiplash Injuries
Status: Enrolling
Updated:  12/31/1969
Northwestern University
mi
from
Chicago, IL
Neuromuscular Mechanisms Underlying Poor Recovery From Whiplash Injuries
Neuromuscular Mechanisms Underlying Poor Recovery From Whiplash Injuries
Status: Enrolling
Updated: 12/31/1969
Northwestern University
mi
from
Chicago, IL
Click here to add this to my saved trials
PRIORITI-MTF Study- Testing Patient Response to the IDEO
Patient Response to an Integrated Orthotic and Rehabilitation Initiative for Traumatic Injuries for the Military Treatment Facilities (PRIORITI-MTF)
Status: Enrolling
Updated:  12/31/1969
Naval Medical Center - San Diego
mi
from
San Diego, CA
PRIORITI-MTF Study- Testing Patient Response to the IDEO
Patient Response to an Integrated Orthotic and Rehabilitation Initiative for Traumatic Injuries for the Military Treatment Facilities (PRIORITI-MTF)
Status: Enrolling
Updated: 12/31/1969
Naval Medical Center - San Diego
mi
from
San Diego, CA
Click here to add this to my saved trials
PRIORITI-MTF Study- Testing Patient Response to the IDEO
Patient Response to an Integrated Orthotic and Rehabilitation Initiative for Traumatic Injuries for the Military Treatment Facilities (PRIORITI-MTF)
Status: Enrolling
Updated:  12/31/1969
Walter Reed National Military Medical Center
mi
from
Bethesda, MD
PRIORITI-MTF Study- Testing Patient Response to the IDEO
Patient Response to an Integrated Orthotic and Rehabilitation Initiative for Traumatic Injuries for the Military Treatment Facilities (PRIORITI-MTF)
Status: Enrolling
Updated: 12/31/1969
Walter Reed National Military Medical Center
mi
from
Bethesda, MD
Click here to add this to my saved trials
PRIORITI-MTF Study- Testing Patient Response to the IDEO
Patient Response to an Integrated Orthotic and Rehabilitation Initiative for Traumatic Injuries for the Military Treatment Facilities (PRIORITI-MTF)
Status: Enrolling
Updated:  12/31/1969
San Antonio Center for the Intrepid
mi
from
San Antonio, TX
PRIORITI-MTF Study- Testing Patient Response to the IDEO
Patient Response to an Integrated Orthotic and Rehabilitation Initiative for Traumatic Injuries for the Military Treatment Facilities (PRIORITI-MTF)
Status: Enrolling
Updated: 12/31/1969
San Antonio Center for the Intrepid
mi
from
San Antonio, TX
Click here to add this to my saved trials
Feasibility of Upright Bed Position in ARDS Patients
Feasibility of Upright Bed Position in ARDS Patients
Status: Enrolling
Updated:  12/31/1969
Wake Forest Baptist Health, Medical Intensive Care Unit
mi
from
Winston-Salem, NC
Feasibility of Upright Bed Position in ARDS Patients
Feasibility of Upright Bed Position in ARDS Patients
Status: Enrolling
Updated: 12/31/1969
Wake Forest Baptist Health, Medical Intensive Care Unit
mi
from
Winston-Salem, NC
Click here to add this to my saved trials
Comparison of Two Psycho-educational Family Group Interventions for Persons With SCI and Their Caregivers
Comparison of Two Psycho-educational Family Group Interventions for Persons With SCI and Their Caregivers
Status: Enrolling
Updated:  12/31/1969
St. Luke's Rehabilitation Institute
mi
from
Spokane, WA
Comparison of Two Psycho-educational Family Group Interventions for Persons With SCI and Their Caregivers
Comparison of Two Psycho-educational Family Group Interventions for Persons With SCI and Their Caregivers
Status: Enrolling
Updated: 12/31/1969
St. Luke's Rehabilitation Institute
mi
from
Spokane, WA
Click here to add this to my saved trials
Non-Invasive Shock: Differentiating Shock in the Emergency Department
Non-Invasive Shock: Differentiating Shock in the Emergency Department
Status: Enrolling
Updated:  12/31/1969
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Non-Invasive Shock: Differentiating Shock in the Emergency Department
Non-Invasive Shock: Differentiating Shock in the Emergency Department
Status: Enrolling
Updated: 12/31/1969
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Click here to add this to my saved trials