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

Early Treatment With Dexamethasone in Mild Acute Pancreatitis
Intravenous Dexamethasone for the Early Treatment of Mild Acute Pancreatitis: A Double-Blind, Randomized, Placebo Controlled Trial
Status: Enrolling
Updated:  11/30/2010
Brigham and Women's Hosp
mi
from
Boston, MA
Early Treatment With Dexamethasone in Mild Acute Pancreatitis
Intravenous Dexamethasone for the Early Treatment of Mild Acute Pancreatitis: A Double-Blind, Randomized, Placebo Controlled Trial
Status: Enrolling
Updated: 11/30/2010
Brigham and Women's Hosp
mi
from
Boston, MA
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Developing a Diabetic Foot Ulcer Protocol
Developing a Diabetic Foot Ulcer Protocol in a Multi-ethnic, Underserved Population
Status: Enrolling
Updated:  12/3/2010
Harris County Hospital District Community Health
mi
from
Houston, TX
Developing a Diabetic Foot Ulcer Protocol
Developing a Diabetic Foot Ulcer Protocol in a Multi-ethnic, Underserved Population
Status: Enrolling
Updated: 12/3/2010
Harris County Hospital District Community Health
mi
from
Houston, TX
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Validation of Esophageal Variceal Grading: A Comparative Study of Upper Gastrointestinal (GI) Endoscopy and Capsule Endoscopy
Validation of Esophageal Variceal Grading: A Comparative Study of Upper Gastrointestinal (GI) Endoscopy and Capsule Endoscopy
Status: Enrolling
Updated:  12/15/2010
Johns Hopkins Hospital
mi
from
Baltimore, MD
Validation of Esophageal Variceal Grading: A Comparative Study of Upper Gastrointestinal (GI) Endoscopy and Capsule Endoscopy
Validation of Esophageal Variceal Grading: A Comparative Study of Upper Gastrointestinal (GI) Endoscopy and Capsule Endoscopy
Status: Enrolling
Updated: 12/15/2010
Johns Hopkins Hospital
mi
from
Baltimore, MD
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Trial of 70% Ethanol Versus Heparin to Reduce the Rate of Central Line Infections in Children With Short Bowel Syndrome
Status: Enrolling
Updated:  12/28/2010
Children's Hospital Boston
mi
from
Boston, MA
Trial of 70% Ethanol Versus Heparin to Reduce the Rate of Central Line Infections in Children With Short Bowel Syndrome
Status: Enrolling
Updated: 12/28/2010
Children's Hospital Boston
mi
from
Boston, MA
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Rifaximin Versus Lactulose in Renal Failure
A Randomized Comparison of Rifaximin Versus Lactulose in Hospitalized Cirrhotic Patients With Progressive Renal Failure
Status: Enrolling
Updated:  1/3/2011
Weill Cornell Medical Center
mi
from
New York, NY
Rifaximin Versus Lactulose in Renal Failure
A Randomized Comparison of Rifaximin Versus Lactulose in Hospitalized Cirrhotic Patients With Progressive Renal Failure
Status: Enrolling
Updated: 1/3/2011
Weill Cornell Medical Center
mi
from
New York, NY
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Randomized Comparison of Two Albumin Administration Schedules for Spontaneous Bacterial Peritonitis (SBP)
A Randomized Comparison of Two Albumin Administration Schedules for Spontaneous Bacterial Peritonitis
Status: Enrolling
Updated:  1/3/2011
New York Presbyterian Hospital-Weill Cornell Medical Center
mi
from
New York, NY
Randomized Comparison of Two Albumin Administration Schedules for Spontaneous Bacterial Peritonitis (SBP)
A Randomized Comparison of Two Albumin Administration Schedules for Spontaneous Bacterial Peritonitis
Status: Enrolling
Updated: 1/3/2011
New York Presbyterian Hospital-Weill Cornell Medical Center
mi
from
New York, NY
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Randomized Comparison of Two Albumin Administration Schedules for Spontaneous Bacterial Peritonitis (SBP)
A Randomized Comparison of Two Albumin Administration Schedules for Spontaneous Bacterial Peritonitis
Status: Enrolling
Updated:  1/3/2011
New York Presbyterian Hospital - Columbia University Medical Center
mi
from
New York, NY
Randomized Comparison of Two Albumin Administration Schedules for Spontaneous Bacterial Peritonitis (SBP)
A Randomized Comparison of Two Albumin Administration Schedules for Spontaneous Bacterial Peritonitis
Status: Enrolling
Updated: 1/3/2011
New York Presbyterian Hospital - Columbia University Medical Center
mi
from
New York, NY
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Rectal Sensory Training - A Study of Two Techniques
Rectal Sensory Training - A Randomized Controlled Study of Two Techniques
Status: Enrolling
Updated:  2/18/2011
University of Iowa Hospitals and Clinics
mi
from
Iowa City, IA
Rectal Sensory Training - A Study of Two Techniques
Rectal Sensory Training - A Randomized Controlled Study of Two Techniques
Status: Enrolling
Updated: 2/18/2011
University of Iowa Hospitals and Clinics
mi
from
Iowa City, IA
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End Stage Liver Disease and Body Composition Assessment: Utilizing Bioelectric Impedance Analysis (BIA)
End Stage Liver Disease and Body Composition Assessment: Utilizing Bioelectric Impedance Analysis (BIA)
Status: Enrolling
Updated:  3/3/2011
University of Cincinnati
mi
from
Cincinnati, OH
End Stage Liver Disease and Body Composition Assessment: Utilizing Bioelectric Impedance Analysis (BIA)
End Stage Liver Disease and Body Composition Assessment: Utilizing Bioelectric Impedance Analysis (BIA)
Status: Enrolling
Updated: 3/3/2011
University of Cincinnati
mi
from
Cincinnati, OH
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Pravastatin Therapy in Patients With Active Crohn's Disease: A Pilot Study
Pravastatin Therapy in Patients With Active Crohn's Disease: A Pilot Study
Status: Enrolling
Updated:  3/4/2011
University of Virginia
mi
from
Charlottesville, VA
Pravastatin Therapy in Patients With Active Crohn's Disease: A Pilot Study
Pravastatin Therapy in Patients With Active Crohn's Disease: A Pilot Study
Status: Enrolling
Updated: 3/4/2011
University of Virginia
mi
from
Charlottesville, VA
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EnSeal Efficacy and Bursting Pressure in Human Vessels
EnSeal Efficacy and Bursting Pressure in Human Vessels
Status: Enrolling
Updated:  3/9/2011
University of Illinois Medical Center, Chicago
mi
from
Chicago, IL
EnSeal Efficacy and Bursting Pressure in Human Vessels
EnSeal Efficacy and Bursting Pressure in Human Vessels
Status: Enrolling
Updated: 3/9/2011
University of Illinois Medical Center, Chicago
mi
from
Chicago, IL
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Erlotinib Hydrochloride in Treating Patients With Previously Treated Non-Small Cell Lung Cancer, Head and Neck Cancer, or Esophageal Cancer and Precancerous Lesions of the Lung
A Phase I Study of Erlotinib in Patients With Premalignant Lesions of the Lung
Status: Enrolling
Updated:  3/9/2011
Northwestern University
mi
from
Chicago, IL
Erlotinib Hydrochloride in Treating Patients With Previously Treated Non-Small Cell Lung Cancer, Head and Neck Cancer, or Esophageal Cancer and Precancerous Lesions of the Lung
A Phase I Study of Erlotinib in Patients With Premalignant Lesions of the Lung
Status: Enrolling
Updated: 3/9/2011
Northwestern University
mi
from
Chicago, IL
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Erlotinib Hydrochloride in Treating Patients With Previously Treated Non-Small Cell Lung Cancer, Head and Neck Cancer, or Esophageal Cancer and Precancerous Lesions of the Lung
A Phase I Study of Erlotinib in Patients With Premalignant Lesions of the Lung
Status: Enrolling
Updated:  3/9/2011
Roswell Park Cancer Institute
mi
from
Buffalo, NY
Erlotinib Hydrochloride in Treating Patients With Previously Treated Non-Small Cell Lung Cancer, Head and Neck Cancer, or Esophageal Cancer and Precancerous Lesions of the Lung
A Phase I Study of Erlotinib in Patients With Premalignant Lesions of the Lung
Status: Enrolling
Updated: 3/9/2011
Roswell Park Cancer Institute
mi
from
Buffalo, NY
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CCRC: A Project of the Treatment of HIV Enteropathy With ImmunoLin® Supplements
CCRC: A Pilot Project of the Treatment of HIV Enteropathy With ImmunoLin® Supplements
Status: Enrolling
Updated:  3/11/2011
UCD CTSC Clinical Research Center (CCRC)
mi
from
Mather, CA
CCRC: A Project of the Treatment of HIV Enteropathy With ImmunoLin® Supplements
CCRC: A Pilot Project of the Treatment of HIV Enteropathy With ImmunoLin® Supplements
Status: Enrolling
Updated: 3/11/2011
UCD CTSC Clinical Research Center (CCRC)
mi
from
Mather, CA
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Study of Computer-Based Treatment for Drug Dependence
Pilot Trial of a Therapeutic Interactive Voice Response System for Buprenorphine Maintenance: The Recovery Line Support System
Status: Enrolling
Updated:  3/14/2011
APT Foundation
mi
from
New Haven, CT
Study of Computer-Based Treatment for Drug Dependence
Pilot Trial of a Therapeutic Interactive Voice Response System for Buprenorphine Maintenance: The Recovery Line Support System
Status: Enrolling
Updated: 3/14/2011
APT Foundation
mi
from
New Haven, CT
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Trial of Compassionate Use of hp802-247 to Treat Venous Leg Ulcers in Subjects Who Have Failed Multiple Other Healing Technologies
TRIAL OF COMPASSIONATE USE OF HP802-247 TO TREAT VENOUS LEG ULCERS IN SUBJECTS WHO HAVE FAILED MULTIPLE OTHER HEALING TECHNOLOGIES
Status: Enrolling
Updated:  3/21/2011
Overlook Hospital Wound Healing Program
mi
from
Summit, NJ
Trial of Compassionate Use of hp802-247 to Treat Venous Leg Ulcers in Subjects Who Have Failed Multiple Other Healing Technologies
TRIAL OF COMPASSIONATE USE OF HP802-247 TO TREAT VENOUS LEG ULCERS IN SUBJECTS WHO HAVE FAILED MULTIPLE OTHER HEALING TECHNOLOGIES
Status: Enrolling
Updated: 3/21/2011
Overlook Hospital Wound Healing Program
mi
from
Summit, NJ
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Comparison of Acid Reflux at Two Levels in the Esophagus Using the BRAVO Capsule
Evaluation of Esophageal and Gastric Acid Levels in Patients Presenting With Upper Gastrointestinal Symptoms Using a Novel PH System
Status: Enrolling
Updated:  3/21/2011
Department of Veterans Affairs Medical Center
mi
from
Kansas City, MO
Comparison of Acid Reflux at Two Levels in the Esophagus Using the BRAVO Capsule
Evaluation of Esophageal and Gastric Acid Levels in Patients Presenting With Upper Gastrointestinal Symptoms Using a Novel PH System
Status: Enrolling
Updated: 3/21/2011
Department of Veterans Affairs Medical Center
mi
from
Kansas City, MO
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Exercise Versus Diet in the Treatment of Nonalcoholic Fatty Liver Disease
Exercise Versus Diet in the Treatment of Nonalcoholic Fatty Liver Disease
Status: Enrolling
Updated:  3/31/2011
University Hospital
mi
from
Columbia, MO
Exercise Versus Diet in the Treatment of Nonalcoholic Fatty Liver Disease
Exercise Versus Diet in the Treatment of Nonalcoholic Fatty Liver Disease
Status: Enrolling
Updated: 3/31/2011
University Hospital
mi
from
Columbia, MO
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Transcranial Direct Current Stimulation (TDCS) for Facilitating Swallowing Improvement After an Acute Unilateral Hemispheric Stroke
Pilot Study of Transcranial Direct Current Stimulation for Facilitating Swallowing Improvement After an Acute Unilateral Hemispheric Infarction
Status: Enrolling
Updated:  4/7/2011
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Transcranial Direct Current Stimulation (TDCS) for Facilitating Swallowing Improvement After an Acute Unilateral Hemispheric Stroke
Pilot Study of Transcranial Direct Current Stimulation for Facilitating Swallowing Improvement After an Acute Unilateral Hemispheric Infarction
Status: Enrolling
Updated: 4/7/2011
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
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Non-invasive Imaging of GI Inflammation Using Microbubble Contrast Enhanced Ultrasonography
Non-invasive Imaging of GI Inflammation Using Microbubble Contrast Enhanced Ultrasonography
Status: Enrolling
Updated:  4/25/2011
University of Virginia
mi
from
Charlottesville, VA
Non-invasive Imaging of GI Inflammation Using Microbubble Contrast Enhanced Ultrasonography
Non-invasive Imaging of GI Inflammation Using Microbubble Contrast Enhanced Ultrasonography
Status: Enrolling
Updated: 4/25/2011
University of Virginia
mi
from
Charlottesville, VA
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Topical Bethanechol for Improvement of Esophageal Dysmotility
Topical Bethanechol for Improvement of Esophageal Dysmotility: A Pilot Study
Status: Enrolling
Updated:  5/12/2011
Med College of Georgia
mi
from
Augusta, GA
Topical Bethanechol for Improvement of Esophageal Dysmotility
Topical Bethanechol for Improvement of Esophageal Dysmotility: A Pilot Study
Status: Enrolling
Updated: 5/12/2011
Med College of Georgia
mi
from
Augusta, GA
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Effect of Vitamin D Supplementation on Hemoglobin A1c
Does Vitamin D Supplement Alter Serum Level of Glycosylated Hemoglobin in Adult Patients Between 34-74 Years With Type 2 Diabetes Mellitus and Vitamin D Deficiency?
Status: Enrolling
Updated:  5/13/2011
Genesys East Flint Campus Clinic
mi
from
Flint, MI
Effect of Vitamin D Supplementation on Hemoglobin A1c
Does Vitamin D Supplement Alter Serum Level of Glycosylated Hemoglobin in Adult Patients Between 34-74 Years With Type 2 Diabetes Mellitus and Vitamin D Deficiency?
Status: Enrolling
Updated: 5/13/2011
Genesys East Flint Campus Clinic
mi
from
Flint, MI
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Impact of Emergency Department Probiotic Treatment of Pediatric Gastroenteritis
Impact of Emergency Department Probiotic Treatment of Pediatric Gastroenteritis: Randomized Controlled Trial
Status: Enrolling
Updated:  5/17/2011
Childrens National Medical Center
mi
from
Washington,
Impact of Emergency Department Probiotic Treatment of Pediatric Gastroenteritis
Impact of Emergency Department Probiotic Treatment of Pediatric Gastroenteritis: Randomized Controlled Trial
Status: Enrolling
Updated: 5/17/2011
Childrens National Medical Center
mi
from
Washington,
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Impact of Emergency Department Probiotic Treatment of Pediatric Gastroenteritis
Impact of Emergency Department Probiotic Treatment of Pediatric Gastroenteritis: Randomized Controlled Trial
Status: Enrolling
Updated:  5/17/2011
Ann & Robert H. Lurie Children's Hospital of Chicago
mi
from
Chicago, IL
Impact of Emergency Department Probiotic Treatment of Pediatric Gastroenteritis
Impact of Emergency Department Probiotic Treatment of Pediatric Gastroenteritis: Randomized Controlled Trial
Status: Enrolling
Updated: 5/17/2011
Ann & Robert H. Lurie Children's Hospital of Chicago
mi
from
Chicago, IL
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Impact of Emergency Department Probiotic Treatment of Pediatric Gastroenteritis
Impact of Emergency Department Probiotic Treatment of Pediatric Gastroenteritis: Randomized Controlled Trial
Status: Enrolling
Updated:  5/17/2011
Morgan Stanley Children's Hospital of New York
mi
from
New York, NY
Impact of Emergency Department Probiotic Treatment of Pediatric Gastroenteritis
Impact of Emergency Department Probiotic Treatment of Pediatric Gastroenteritis: Randomized Controlled Trial
Status: Enrolling
Updated: 5/17/2011
Morgan Stanley Children's Hospital of New York
mi
from
New York, NY
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Impact of Emergency Department Probiotic Treatment of Pediatric Gastroenteritis
Impact of Emergency Department Probiotic Treatment of Pediatric Gastroenteritis: Randomized Controlled Trial
Status: Enrolling
Updated:  5/17/2011
Children's Hospital of Wisconsin
mi
from
Milwaukee, WI
Impact of Emergency Department Probiotic Treatment of Pediatric Gastroenteritis
Impact of Emergency Department Probiotic Treatment of Pediatric Gastroenteritis: Randomized Controlled Trial
Status: Enrolling
Updated: 5/17/2011
Children's Hospital of Wisconsin
mi
from
Milwaukee, WI
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Silk-Like Fabric for the Prevention of Pressure Sores in a Long Term Care Setting
Evaluate the Efficacy of a Silk-Like Fabric for the Prevention of Pressure Sores in a Long Term Care Setting
Status: Enrolling
Updated:  5/17/2011
Durham VA Medical Center
mi
from
Durham, NC
Silk-Like Fabric for the Prevention of Pressure Sores in a Long Term Care Setting
Evaluate the Efficacy of a Silk-Like Fabric for the Prevention of Pressure Sores in a Long Term Care Setting
Status: Enrolling
Updated: 5/17/2011
Durham VA Medical Center
mi
from
Durham, NC
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Regression of Myocardial Steatosis by Nebivolol
Status: Enrolling
Updated:  5/20/2011
Cedars-Sinai Medical Center
mi
from
Los Angeles, CA
Regression of Myocardial Steatosis by Nebivolol
Status: Enrolling
Updated: 5/20/2011
Cedars-Sinai Medical Center
mi
from
Los Angeles, CA
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Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Foot Ulcers
A Prospective, Randomized Comparative Parallel Study of Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Foot Ulcers
Status: Enrolling
Updated:  6/6/2011
Advanced Foot Care and Clinincal Research Center
mi
from
Fresno, CA
Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Foot Ulcers
A Prospective, Randomized Comparative Parallel Study of Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Foot Ulcers
Status: Enrolling
Updated: 6/6/2011
Advanced Foot Care and Clinincal Research Center
mi
from
Fresno, CA
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Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Foot Ulcers
A Prospective, Randomized Comparative Parallel Study of Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Foot Ulcers
Status: Enrolling
Updated:  6/6/2011
Professional Education and Research Institute
mi
from
Roanoke, VA
Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Foot Ulcers
A Prospective, Randomized Comparative Parallel Study of Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Foot Ulcers
Status: Enrolling
Updated: 6/6/2011
Professional Education and Research Institute
mi
from
Roanoke, VA
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A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
Arrowhead Regional Medical Center
mi
from
Colton, CA
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
Arrowhead Regional Medical Center
mi
from
Colton, CA
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A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
UCSD Medical Center
mi
from
San Diego, CA
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
UCSD Medical Center
mi
from
San Diego, CA
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A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
Georgetown University Hospital
mi
from
Washington,
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
Georgetown University Hospital
mi
from
Washington,
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A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
Kapiolani Medical Center for Women and Children
mi
from
Honolulu, HI
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
Kapiolani Medical Center for Women and Children
mi
from
Honolulu, HI
Click here to add this to my saved trials
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
University of Louisville
mi
from
Louisville, KY
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
University of Louisville
mi
from
Louisville, KY
Click here to add this to my saved trials
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
William Beaumont Hospital-Royal Oak
mi
from
Royal Oak, MI
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
William Beaumont Hospital-Royal Oak
mi
from
Royal Oak, MI
Click here to add this to my saved trials
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
St. John's Mercy Medical Center
mi
from
St. Louis, MO
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
St. John's Mercy Medical Center
mi
from
St. Louis, MO
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A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
Brooklyn Hospital Center
mi
from
Brooklyn, NY
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
Brooklyn Hospital Center
mi
from
Brooklyn, NY
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A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
Stony Brook University Medical Center
mi
from
Stony Brook, NY
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
Stony Brook University Medical Center
mi
from
Stony Brook, NY
Click here to add this to my saved trials
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
Westchester Medical Center
mi
from
Valhalla, NY
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
Westchester Medical Center
mi
from
Valhalla, NY
Click here to add this to my saved trials
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
ECU Brody School of Medicine
mi
from
Greenville, NC
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
ECU Brody School of Medicine
mi
from
Greenville, NC
Click here to add this to my saved trials
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
Cincinnati Children's Hospital Medical Center
mi
from
Cincinnati, OH
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
Cincinnati Children's Hospital Medical Center
mi
from
Cincinnati, OH
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A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
University Hospitals of Cleveland
mi
from
Cleveland, OH
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
University Hospitals of Cleveland
mi
from
Cleveland, OH
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A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
St. Vincent Mercy Children's Hospital
mi
from
Toledo, OH
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
St. Vincent Mercy Children's Hospital
mi
from
Toledo, OH
Click here to add this to my saved trials
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
Jefferson duPont Children's Health Program
mi
from
Philadelphia, PA
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
Jefferson duPont Children's Health Program
mi
from
Philadelphia, PA
Click here to add this to my saved trials
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
Drexel University College of Medicine, Clinical Research Group
mi
from
Philadelphia, PA
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
Drexel University College of Medicine, Clinical Research Group
mi
from
Philadelphia, PA
Click here to add this to my saved trials
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
Albert Einstein Medical Center
mi
from
Philadelphia, PA
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
Albert Einstein Medical Center
mi
from
Philadelphia, PA
Click here to add this to my saved trials
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
Virginia Commonwealth University
mi
from
Richmond, VA
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
Virginia Commonwealth University
mi
from
Richmond, VA
Click here to add this to my saved trials
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated:  6/10/2011
West Virginia University
mi
from
Morgantown, WV
A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia
Status: Enrolling
Updated: 6/10/2011
West Virginia University
mi
from
Morgantown, WV
Click here to add this to my saved trials
Safety and Pharmacokinetics Study of HE3286 in Patients With Active, Mild-to-Moderate Ulcerative Colitis
A Phase I/II, Double-Blind, Randomized, Placebo-Controlled, Dose Ranging Study of the Safety, Tolerance, Pharmacokinetics and Activity of HE3286 When Administered Orally to Patients With Active, Mild-to-Moderate Ulcerative Colitis
Status: Enrolling
Updated:  6/11/2011
Clinical Research Facility
mi
from
Tucson, AZ
Safety and Pharmacokinetics Study of HE3286 in Patients With Active, Mild-to-Moderate Ulcerative Colitis
A Phase I/II, Double-Blind, Randomized, Placebo-Controlled, Dose Ranging Study of the Safety, Tolerance, Pharmacokinetics and Activity of HE3286 When Administered Orally to Patients With Active, Mild-to-Moderate Ulcerative Colitis
Status: Enrolling
Updated: 6/11/2011
Clinical Research Facility
mi
from
Tucson, AZ
Click here to add this to my saved trials