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
20,707
archived clinical trials in
Gastrointestinal

Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated:  11/21/2017
Clinical Research Facility
mi
from
Cincinnati, OH
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated: 11/21/2017
Clinical Research Facility
mi
from
Cincinnati, OH
Click here to add this to my saved trials
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated:  11/21/2017
Clinical Research Facility
mi
from
Cincinnati, OH
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated: 11/21/2017
Clinical Research Facility
mi
from
Cincinnati, OH
Click here to add this to my saved trials
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated:  11/21/2017
Clinical Research Facility
mi
from
Chattanooga, TN
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated: 11/21/2017
Clinical Research Facility
mi
from
Chattanooga, TN
Click here to add this to my saved trials
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated:  11/21/2017
Clinical Research Facility
mi
from
Germantown, TN
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated: 11/21/2017
Clinical Research Facility
mi
from
Germantown, TN
Click here to add this to my saved trials
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated:  11/21/2017
Clinical Research Facility
mi
from
Houston, TX
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated: 11/21/2017
Clinical Research Facility
mi
from
Houston, TX
Click here to add this to my saved trials
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated:  11/21/2017
Clinical Research Facility
mi
from
Live Oak, TX
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated: 11/21/2017
Clinical Research Facility
mi
from
Live Oak, TX
Click here to add this to my saved trials
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated:  11/21/2017
Clinical Research Facility
mi
from
San Antonio, TX
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated: 11/21/2017
Clinical Research Facility
mi
from
San Antonio, TX
Click here to add this to my saved trials
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated:  11/21/2017
Clinical Research Facility
mi
from
San Antonio, TX
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated: 11/21/2017
Clinical Research Facility
mi
from
San Antonio, TX
Click here to add this to my saved trials
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated:  11/21/2017
Clinical Research Facility
mi
from
Salt Lake City, UT
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated: 11/21/2017
Clinical Research Facility
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated:  11/21/2017
Clinical Research Facility
mi
from
Richmond, VA
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated: 11/21/2017
Clinical Research Facility
mi
from
Richmond, VA
Click here to add this to my saved trials
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated:  11/21/2017
Clinical Research Facility
mi
from
Richmond, VA
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated: 11/21/2017
Clinical Research Facility
mi
from
Richmond, VA
Click here to add this to my saved trials
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated:  11/21/2017
Clinical Research Facility
mi
from
Seattle, WA
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated: 11/21/2017
Clinical Research Facility
mi
from
Seattle, WA
Click here to add this to my saved trials
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated:  11/21/2017
Clinical Research Facility
mi
from
Seattle, WA
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated: 11/21/2017
Clinical Research Facility
mi
from
Seattle, WA
Click here to add this to my saved trials
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated:  11/21/2017
Clinical Research Facility
mi
from
Phoenix, AZ
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated: 11/21/2017
Clinical Research Facility
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated:  11/21/2017
Clinical Research Facility
mi
from
Louisville, KY
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated: 11/21/2017
Clinical Research Facility
mi
from
Louisville, KY
Click here to add this to my saved trials
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated:  11/21/2017
Clinical Research Facility
mi
from
Saint Paul, MN
Efficacy and Safety Study of Cenicriviroc for the Treatment of NASH in Adult Subjects With Liver Fibrosis
CENTAUR: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects With Liver Fibrosis
Status: Enrolling
Updated: 11/21/2017
Clinical Research Facility
mi
from
Saint Paul, MN
Click here to add this to my saved trials
Effect of Acupuncture on Symptoms of Diarrhea and Pain in IBS
Effect of Acupuncture on Symptoms of Diarrhea and Pain in Diarrhea Predominant Irritable Bowel Syndrome (IBS) and Effect on Plasma Beta-endorphin and Serotonin Levels.
Status: Enrolling
Updated:  11/21/2017
Hershey Medical Center
mi
from
Hershey, PA
Effect of Acupuncture on Symptoms of Diarrhea and Pain in IBS
Effect of Acupuncture on Symptoms of Diarrhea and Pain in Diarrhea Predominant Irritable Bowel Syndrome (IBS) and Effect on Plasma Beta-endorphin and Serotonin Levels.
Status: Enrolling
Updated: 11/21/2017
Hershey Medical Center
mi
from
Hershey, PA
Click here to add this to my saved trials
Ursodiol in Treating Patients With Barrett Esophagus and Low-Grade Dysplasia
Clinical Study of Ursodeoxycholic Acid in Barrett's Patients
Status: Enrolling
Updated:  11/22/2017
Southern Arizona Veterans Affairs Health Center
mi
from
Tucson, AZ
Ursodiol in Treating Patients With Barrett Esophagus and Low-Grade Dysplasia
Clinical Study of Ursodeoxycholic Acid in Barrett's Patients
Status: Enrolling
Updated: 11/22/2017
Southern Arizona Veterans Affairs Health Center
mi
from
Tucson, AZ
Click here to add this to my saved trials
Ursodiol in Treating Patients With Barrett Esophagus and Low-Grade Dysplasia
Clinical Study of Ursodeoxycholic Acid in Barrett's Patients
Status: Enrolling
Updated:  11/22/2017
University of Arizona Health Sciences Center
mi
from
Tucson, AZ
Ursodiol in Treating Patients With Barrett Esophagus and Low-Grade Dysplasia
Clinical Study of Ursodeoxycholic Acid in Barrett's Patients
Status: Enrolling
Updated: 11/22/2017
University of Arizona Health Sciences Center
mi
from
Tucson, AZ
Click here to add this to my saved trials
Ursodiol in Treating Patients With Barrett Esophagus and Low-Grade Dysplasia
Clinical Study of Ursodeoxycholic Acid in Barrett's Patients
Status: Enrolling
Updated:  11/22/2017
Univ of North Carolina
mi
from
Chapel Hill, NC
Ursodiol in Treating Patients With Barrett Esophagus and Low-Grade Dysplasia
Clinical Study of Ursodeoxycholic Acid in Barrett's Patients
Status: Enrolling
Updated: 11/22/2017
Univ of North Carolina
mi
from
Chapel Hill, NC
Click here to add this to my saved trials
Ursodiol in Treating Patients With Barrett Esophagus and Low-Grade Dysplasia
Clinical Study of Ursodeoxycholic Acid in Barrett's Patients
Status: Enrolling
Updated:  11/22/2017
Arizona Cancer Center-North Campus
mi
from
Tucson, AZ
Ursodiol in Treating Patients With Barrett Esophagus and Low-Grade Dysplasia
Clinical Study of Ursodeoxycholic Acid in Barrett's Patients
Status: Enrolling
Updated: 11/22/2017
Arizona Cancer Center-North Campus
mi
from
Tucson, AZ
Click here to add this to my saved trials
PK Study of T-817 in Subjects With Hepatic Impairment
A Phase 1, Two-Part, Open-Label, Parallel-Cohort, Single-Dose Study to Determine the Pharmacokinetics of T-817MA in Adult Subjects With Hepatic Impairment and in Healthy Adult Subjects
Status: Enrolling
Updated:  11/22/2017
University of Miami
mi
from
Miami, FL
PK Study of T-817 in Subjects With Hepatic Impairment
A Phase 1, Two-Part, Open-Label, Parallel-Cohort, Single-Dose Study to Determine the Pharmacokinetics of T-817MA in Adult Subjects With Hepatic Impairment and in Healthy Adult Subjects
Status: Enrolling
Updated: 11/22/2017
University of Miami
mi
from
Miami, FL
Click here to add this to my saved trials
PK Study of T-817 in Subjects With Hepatic Impairment
A Phase 1, Two-Part, Open-Label, Parallel-Cohort, Single-Dose Study to Determine the Pharmacokinetics of T-817MA in Adult Subjects With Hepatic Impairment and in Healthy Adult Subjects
Status: Enrolling
Updated:  11/22/2017
Orlando Clinical Research Center
mi
from
Orlando, FL
PK Study of T-817 in Subjects With Hepatic Impairment
A Phase 1, Two-Part, Open-Label, Parallel-Cohort, Single-Dose Study to Determine the Pharmacokinetics of T-817MA in Adult Subjects With Hepatic Impairment and in Healthy Adult Subjects
Status: Enrolling
Updated: 11/22/2017
Orlando Clinical Research Center
mi
from
Orlando, FL
Click here to add this to my saved trials
Mitomycin as a Hyperthermic Peritoneal Perfusion in Treating Patients With Malignant Ascites
Phase II Study of Laparoscopic Hyperthermic Peritoneal Chemotherapy for Malignant Ascites
Status: Enrolling
Updated:  11/27/2017
University of Minnesota Cancer Center
mi
from
Minneapolis, MN
Mitomycin as a Hyperthermic Peritoneal Perfusion in Treating Patients With Malignant Ascites
Phase II Study of Laparoscopic Hyperthermic Peritoneal Chemotherapy for Malignant Ascites
Status: Enrolling
Updated: 11/27/2017
University of Minnesota Cancer Center
mi
from
Minneapolis, MN
Click here to add this to my saved trials
Patient-Controlled Sedation Versus Anesthesiologist-Administered Sedation
A Phase IV, Randomized, Double-Blind, Controlled Study of the Effects of Patient-Controlled Sedation vs. Anesthesiologist-Administered Sedation With Propofol and Remifentanil on Rate of Disordered Breathing in Subjects Undergoing Elective Colonoscopy
Status: Enrolling
Updated:  11/28/2017
Univ of Pennsylvania
mi
from
Philadelphia, PA
Patient-Controlled Sedation Versus Anesthesiologist-Administered Sedation
A Phase IV, Randomized, Double-Blind, Controlled Study of the Effects of Patient-Controlled Sedation vs. Anesthesiologist-Administered Sedation With Propofol and Remifentanil on Rate of Disordered Breathing in Subjects Undergoing Elective Colonoscopy
Status: Enrolling
Updated: 11/28/2017
Univ of Pennsylvania
mi
from
Philadelphia, PA
Click here to add this to my saved trials
Employment-Based Depot Naltrexone Clinical Trial
Employment-Based Depot Naltrexone Clinical Trial
Status: Enrolling
Updated:  11/29/2017
The Center for Learning and Health
mi
from
Baltimore, MD
Employment-Based Depot Naltrexone Clinical Trial
Employment-Based Depot Naltrexone Clinical Trial
Status: Enrolling
Updated: 11/29/2017
The Center for Learning and Health
mi
from
Baltimore, MD
Click here to add this to my saved trials
IL-2 Expressing, Attenuated Salmonella Typhimurium in Unresectable Hepatic Spread
A Phase 1 Study of an IL-2 Expressing, Attenuated Salmonella Typhimurium in Patients With Unresectable Hepatic Spread From Any Non-Hematologic Primary
Status: Enrolling
Updated:  11/29/2017
Edward W. Greeno, MD
mi
from
Minneapolis, MN
IL-2 Expressing, Attenuated Salmonella Typhimurium in Unresectable Hepatic Spread
A Phase 1 Study of an IL-2 Expressing, Attenuated Salmonella Typhimurium in Patients With Unresectable Hepatic Spread From Any Non-Hematologic Primary
Status: Enrolling
Updated: 11/29/2017
Edward W. Greeno, MD
mi
from
Minneapolis, MN
Click here to add this to my saved trials
NIR-Guided Sentinel Lymph-Node Mapping for Esophageal Cancer
Intraoperative NIR-Guided Sentinel Lymph Node Mapping in Esophageal Cancer
Status: Enrolling
Updated:  11/29/2017
Brigham and Women's Hosp
mi
from
Boston, MA
NIR-Guided Sentinel Lymph-Node Mapping for Esophageal Cancer
Intraoperative NIR-Guided Sentinel Lymph Node Mapping in Esophageal Cancer
Status: Enrolling
Updated: 11/29/2017
Brigham and Women's Hosp
mi
from
Boston, MA
Click here to add this to my saved trials
NIR-Guided Sentinel Lymph-Node Mapping for Esophageal Cancer
Intraoperative NIR-Guided Sentinel Lymph Node Mapping in Esophageal Cancer
Status: Enrolling
Updated:  11/29/2017
Dana-Farber Cancer Institute
mi
from
Boston, MA
NIR-Guided Sentinel Lymph-Node Mapping for Esophageal Cancer
Intraoperative NIR-Guided Sentinel Lymph Node Mapping in Esophageal Cancer
Status: Enrolling
Updated: 11/29/2017
Dana-Farber Cancer Institute
mi
from
Boston, MA
Click here to add this to my saved trials
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Status: Enrolling
Updated:  11/29/2017
Childrens Hospital Los Angeles
mi
from
Los Angeles, CA
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Status: Enrolling
Updated: 11/29/2017
Childrens Hospital Los Angeles
mi
from
Los Angeles, CA
Click here to add this to my saved trials
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Status: Enrolling
Updated:  11/29/2017
Children's Mercy Hospital
mi
from
Kansas City, MO
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Status: Enrolling
Updated: 11/29/2017
Children's Mercy Hospital
mi
from
Kansas City, MO
Click here to add this to my saved trials
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Status: Enrolling
Updated:  11/29/2017
Nationwide Children's Hospital
mi
from
Columbus, OH
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Status: Enrolling
Updated: 11/29/2017
Nationwide Children's Hospital
mi
from
Columbus, OH
Click here to add this to my saved trials
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Status: Enrolling
Updated:  11/29/2017
Brown University, Lifespan
mi
from
Providence, RI
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Status: Enrolling
Updated: 11/29/2017
Brown University, Lifespan
mi
from
Providence, RI
Click here to add this to my saved trials
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Status: Enrolling
Updated:  11/29/2017
University of Utah / Primary Children's Hospital
mi
from
Salt Lake City, UT
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Implementation of a Molecular Diagnostic for Pediatric Acute Gastroenteritis: The FilmArray GI Panel IMPACT Study
Status: Enrolling
Updated: 11/29/2017
University of Utah / Primary Children's Hospital
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
A Study With Primatrix Dermal Repair Scaffold For The Treatment Of Diabetic Foot Ulcers
A Multi-Center, Prospective, Randomized Study With Primatrix Dermal Repair Scaffold For The Treatment Of Diabetic Foot Ulcers
Status: Enrolling
Updated:  11/30/2017
HyperbaRXs
mi
from
Cumming, GA
A Study With Primatrix Dermal Repair Scaffold For The Treatment Of Diabetic Foot Ulcers
A Multi-Center, Prospective, Randomized Study With Primatrix Dermal Repair Scaffold For The Treatment Of Diabetic Foot Ulcers
Status: Enrolling
Updated: 11/30/2017
HyperbaRXs
mi
from
Cumming, GA
Click here to add this to my saved trials
A Study With Primatrix Dermal Repair Scaffold For The Treatment Of Diabetic Foot Ulcers
A Multi-Center, Prospective, Randomized Study With Primatrix Dermal Repair Scaffold For The Treatment Of Diabetic Foot Ulcers
Status: Enrolling
Updated:  11/30/2017
Covenant Medical Center
mi
from
Saginaw, MI
A Study With Primatrix Dermal Repair Scaffold For The Treatment Of Diabetic Foot Ulcers
A Multi-Center, Prospective, Randomized Study With Primatrix Dermal Repair Scaffold For The Treatment Of Diabetic Foot Ulcers
Status: Enrolling
Updated: 11/30/2017
Covenant Medical Center
mi
from
Saginaw, MI
Click here to add this to my saved trials
A Study With Primatrix Dermal Repair Scaffold For The Treatment Of Diabetic Foot Ulcers
A Multi-Center, Prospective, Randomized Study With Primatrix Dermal Repair Scaffold For The Treatment Of Diabetic Foot Ulcers
Status: Enrolling
Updated:  11/30/2017
Professional Hospital
mi
from
Guaynabo,
A Study With Primatrix Dermal Repair Scaffold For The Treatment Of Diabetic Foot Ulcers
A Multi-Center, Prospective, Randomized Study With Primatrix Dermal Repair Scaffold For The Treatment Of Diabetic Foot Ulcers
Status: Enrolling
Updated: 11/30/2017
Professional Hospital
mi
from
Guaynabo,
Click here to add this to my saved trials
Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
A Multicenter, Prospective, Randomized, Parallel-group, Standard of Care-controlled Clinical Trial to Evaluate the Use of AMNIOEXCEL® in the Management of Chronic Diabetic Foot Ulcers
Status: Enrolling
Updated:  11/30/2017
Associated Foot & Ankle Specialists, LLC
mi
from
Phoenix, AZ
Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
A Multicenter, Prospective, Randomized, Parallel-group, Standard of Care-controlled Clinical Trial to Evaluate the Use of AMNIOEXCEL® in the Management of Chronic Diabetic Foot Ulcers
Status: Enrolling
Updated: 11/30/2017
Associated Foot & Ankle Specialists, LLC
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
A Multicenter, Prospective, Randomized, Parallel-group, Standard of Care-controlled Clinical Trial to Evaluate the Use of AMNIOEXCEL® in the Management of Chronic Diabetic Foot Ulcers
Status: Enrolling
Updated:  11/30/2017
Center for Clinical Research
mi
from
Castro Valley, CA
Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
A Multicenter, Prospective, Randomized, Parallel-group, Standard of Care-controlled Clinical Trial to Evaluate the Use of AMNIOEXCEL® in the Management of Chronic Diabetic Foot Ulcers
Status: Enrolling
Updated: 11/30/2017
Center for Clinical Research
mi
from
Castro Valley, CA
Click here to add this to my saved trials
Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
A Multicenter, Prospective, Randomized, Parallel-group, Standard of Care-controlled Clinical Trial to Evaluate the Use of AMNIOEXCEL® in the Management of Chronic Diabetic Foot Ulcers
Status: Enrolling
Updated:  11/30/2017
Pacific Wound Center
mi
from
Stockton, CA
Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
A Multicenter, Prospective, Randomized, Parallel-group, Standard of Care-controlled Clinical Trial to Evaluate the Use of AMNIOEXCEL® in the Management of Chronic Diabetic Foot Ulcers
Status: Enrolling
Updated: 11/30/2017
Pacific Wound Center
mi
from
Stockton, CA
Click here to add this to my saved trials
Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
A Multicenter, Prospective, Randomized, Parallel-group, Standard of Care-controlled Clinical Trial to Evaluate the Use of AMNIOEXCEL® in the Management of Chronic Diabetic Foot Ulcers
Status: Enrolling
Updated:  11/30/2017
First Coast Cardiovascular Institute
mi
from
Jacksonville, FL
Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
A Multicenter, Prospective, Randomized, Parallel-group, Standard of Care-controlled Clinical Trial to Evaluate the Use of AMNIOEXCEL® in the Management of Chronic Diabetic Foot Ulcers
Status: Enrolling
Updated: 11/30/2017
First Coast Cardiovascular Institute
mi
from
Jacksonville, FL
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Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
A Multicenter, Prospective, Randomized, Parallel-group, Standard of Care-controlled Clinical Trial to Evaluate the Use of AMNIOEXCEL® in the Management of Chronic Diabetic Foot Ulcers
Status: Enrolling
Updated:  11/30/2017
Beth Israel Deaconess Hospital-Plymouth
mi
from
Plymouth, MA
Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
A Multicenter, Prospective, Randomized, Parallel-group, Standard of Care-controlled Clinical Trial to Evaluate the Use of AMNIOEXCEL® in the Management of Chronic Diabetic Foot Ulcers
Status: Enrolling
Updated: 11/30/2017
Beth Israel Deaconess Hospital-Plymouth
mi
from
Plymouth, MA
Click here to add this to my saved trials
Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
A Multicenter, Prospective, Randomized, Parallel-group, Standard of Care-controlled Clinical Trial to Evaluate the Use of AMNIOEXCEL® in the Management of Chronic Diabetic Foot Ulcers
Status: Enrolling
Updated:  11/30/2017
Duke University
mi
from
Durham, NC
Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
A Multicenter, Prospective, Randomized, Parallel-group, Standard of Care-controlled Clinical Trial to Evaluate the Use of AMNIOEXCEL® in the Management of Chronic Diabetic Foot Ulcers
Status: Enrolling
Updated: 11/30/2017
Duke University
mi
from
Durham, NC
Click here to add this to my saved trials
Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
A Multicenter, Prospective, Randomized, Parallel-group, Standard of Care-controlled Clinical Trial to Evaluate the Use of AMNIOEXCEL® in the Management of Chronic Diabetic Foot Ulcers
Status: Enrolling
Updated:  11/30/2017
Wayne Memorial Hospital
mi
from
Goldsboro, NC
Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
A Multicenter, Prospective, Randomized, Parallel-group, Standard of Care-controlled Clinical Trial to Evaluate the Use of AMNIOEXCEL® in the Management of Chronic Diabetic Foot Ulcers
Status: Enrolling
Updated: 11/30/2017
Wayne Memorial Hospital
mi
from
Goldsboro, NC
Click here to add this to my saved trials
Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
A Multicenter, Prospective, Randomized, Parallel-group, Standard of Care-controlled Clinical Trial to Evaluate the Use of AMNIOEXCEL® in the Management of Chronic Diabetic Foot Ulcers
Status: Enrolling
Updated:  11/30/2017
Barry University Clinical Research
mi
from
North Miami Beach, FL
Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
A Multicenter, Prospective, Randomized, Parallel-group, Standard of Care-controlled Clinical Trial to Evaluate the Use of AMNIOEXCEL® in the Management of Chronic Diabetic Foot Ulcers
Status: Enrolling
Updated: 11/30/2017
Barry University Clinical Research
mi
from
North Miami Beach, FL
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MEDIHONEY® Gel Versus Collagenase for Wound Debridement
"Prospective, Randomized, Multi-Center, Efficacy Non-inferiority Study of MEDIHONEY® Gel Versus Collagenase for Wound Debridement"
Status: Enrolling
Updated:  11/30/2017
Innovative Healing Systems
mi
from
Tampa, FL
MEDIHONEY® Gel Versus Collagenase for Wound Debridement
"Prospective, Randomized, Multi-Center, Efficacy Non-inferiority Study of MEDIHONEY® Gel Versus Collagenase for Wound Debridement"
Status: Enrolling
Updated: 11/30/2017
Innovative Healing Systems
mi
from
Tampa, FL
Click here to add this to my saved trials
Patient Satisfaction With Propofol for Out Patient Colonoscopy
Patient Satisfaction With Propofol for Out Patient Colonoscopy: A Prospective, Randomized, Double-Blind Study
Status: Enrolling
Updated:  11/30/2017
Mount Carmel Health System
mi
from
Columbus, OH
Patient Satisfaction With Propofol for Out Patient Colonoscopy
Patient Satisfaction With Propofol for Out Patient Colonoscopy: A Prospective, Randomized, Double-Blind Study
Status: Enrolling
Updated: 11/30/2017
Mount Carmel Health System
mi
from
Columbus, OH
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A Bridge to Treatment: The Therapeutic Workplace and Methadone Treatment
A Bridge to Treatment: The Therapeutic Workplace and Methadone Treatment
Status: Enrolling
Updated:  12/1/2017
Center for Learning and Health, Johns Hopkins Bayview Medical Campus, 5200 Eastern Ave., Suite W142
mi
from
Baltimore, MD
A Bridge to Treatment: The Therapeutic Workplace and Methadone Treatment
A Bridge to Treatment: The Therapeutic Workplace and Methadone Treatment
Status: Enrolling
Updated: 12/1/2017
Center for Learning and Health, Johns Hopkins Bayview Medical Campus, 5200 Eastern Ave., Suite W142
mi
from
Baltimore, MD
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The Therapeutic Workplace Initiation Study
The Therapeutic Workplace Initiation Study
Status: Enrolling
Updated:  12/1/2017
The Center for Learning and Health
mi
from
Baltimore, MD
The Therapeutic Workplace Initiation Study
The Therapeutic Workplace Initiation Study
Status: Enrolling
Updated: 12/1/2017
The Center for Learning and Health
mi
from
Baltimore, MD
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TD-3504 SAD in Healthy Subjects and Subjects With Ulcerative Colitis (UC)
Study 0146: A Phase 1a, Double-Blinded, Randomized, Placebo Controlled, Single Ascending Dose (SAD) Study to Evaluate the Safety, Tolerability, and Systemic Exposure of TD−3504 in Healthy Subjects and Subjects With Ulcerative Colitis (UC)
Status: Enrolling
Updated:  12/1/2017
Anaheim Clinical Trials, LLC
mi
from
Anaheim, CA
TD-3504 SAD in Healthy Subjects and Subjects With Ulcerative Colitis (UC)
Study 0146: A Phase 1a, Double-Blinded, Randomized, Placebo Controlled, Single Ascending Dose (SAD) Study to Evaluate the Safety, Tolerability, and Systemic Exposure of TD−3504 in Healthy Subjects and Subjects With Ulcerative Colitis (UC)
Status: Enrolling
Updated: 12/1/2017
Anaheim Clinical Trials, LLC
mi
from
Anaheim, CA
Click here to add this to my saved trials