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

Neurobehavioral Measurement of Substance Users in Outpatient Treatment Setting
Neurobehavioral Measurement of Substance Users in an Outpatient Treatment Setting
Status: Enrolling
Updated:  12/31/1969
Hunter Holmes McGuire VA Medical Center
mi
from
Richmond, VA
Neurobehavioral Measurement of Substance Users in Outpatient Treatment Setting
Neurobehavioral Measurement of Substance Users in an Outpatient Treatment Setting
Status: Enrolling
Updated: 12/31/1969
Hunter Holmes McGuire VA Medical Center
mi
from
Richmond, VA
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Videoendoscopic Drainage of Infected Pancreatic Collections
Status: Enrolling
Updated:  12/31/1969
Oregon Health and Sciences University
mi
from
Portland, OR
Videoendoscopic Drainage of Infected Pancreatic Collections
Status: Enrolling
Updated: 12/31/1969
Oregon Health and Sciences University
mi
from
Portland, OR
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Videoendoscopic Drainage of Infected Pancreatic Collections
Status: Enrolling
Updated:  12/31/1969
Veteran's Administration-Portland
mi
from
Portland, OR
Videoendoscopic Drainage of Infected Pancreatic Collections
Status: Enrolling
Updated: 12/31/1969
Veteran's Administration-Portland
mi
from
Portland, OR
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Videoendoscopic Drainage of Infected Pancreatic Collections
Status: Enrolling
Updated:  12/31/1969
Harborview Medical Center
mi
from
Seattle, WA
Videoendoscopic Drainage of Infected Pancreatic Collections
Status: Enrolling
Updated: 12/31/1969
Harborview Medical Center
mi
from
Seattle, WA
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Videoendoscopic Drainage of Infected Pancreatic Collections
Status: Enrolling
Updated:  12/31/1969
Veterans Administration Puget Sound
mi
from
Seattle, WA
Videoendoscopic Drainage of Infected Pancreatic Collections
Status: Enrolling
Updated: 12/31/1969
Veterans Administration Puget Sound
mi
from
Seattle, WA
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Videoendoscopic Drainage of Infected Pancreatic Collections
Status: Enrolling
Updated:  12/31/1969
Univ of Washington
mi
from
Seattle, WA
Videoendoscopic Drainage of Infected Pancreatic Collections
Status: Enrolling
Updated: 12/31/1969
Univ of Washington
mi
from
Seattle, WA
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Videoendoscopic Drainage of Infected Pancreatic Collections
Status: Enrolling
Updated:  12/31/1969
University of Toronto
mi
from
Toronto,
Videoendoscopic Drainage of Infected Pancreatic Collections
Status: Enrolling
Updated: 12/31/1969
University of Toronto
mi
from
Toronto,
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Prospective Evaluation of the Ability of Spyglass Cholangioscopy to Facilitate Radiation Free ERCP
Prospective Evaluation of the Ability of Spyglass Cholangioscopy to Facilitate Radiation Free ERCP
Status: Enrolling
Updated:  12/31/1969
Stanford University School of Medicine
mi
from
Stanford, CA
Prospective Evaluation of the Ability of Spyglass Cholangioscopy to Facilitate Radiation Free ERCP
Prospective Evaluation of the Ability of Spyglass Cholangioscopy to Facilitate Radiation Free ERCP
Status: Enrolling
Updated: 12/31/1969
Stanford University School of Medicine
mi
from
Stanford, CA
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Telescopic Dissection vs. Balloon Dissection During Laparoscopic TEP Inguinal Hernia Repair
Randomized Controlled Trial Comparing Telescopic Dissection vs. Balloon Dissection During Laparoscopic TEP Inguinal Hernia Repair
Status: Enrolling
Updated:  12/31/1969
Cleveland Clinic Comprehensive Hernia Center
mi
from
Cleveland, OH
Telescopic Dissection vs. Balloon Dissection During Laparoscopic TEP Inguinal Hernia Repair
Randomized Controlled Trial Comparing Telescopic Dissection vs. Balloon Dissection During Laparoscopic TEP Inguinal Hernia Repair
Status: Enrolling
Updated: 12/31/1969
Cleveland Clinic Comprehensive Hernia Center
mi
from
Cleveland, OH
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Investigation of Cannabinoid Receptor Agonist Dronabinol in Patients With Functional Chest Pain
Investigation of Cannabinoid Receptor Agonist Dronabinol in Patients With Functional Chest Pain
Status: Enrolling
Updated:  12/31/1969
Temple University Hospital
mi
from
Philadelphia, PA
Investigation of Cannabinoid Receptor Agonist Dronabinol in Patients With Functional Chest Pain
Investigation of Cannabinoid Receptor Agonist Dronabinol in Patients With Functional Chest Pain
Status: Enrolling
Updated: 12/31/1969
Temple University Hospital
mi
from
Philadelphia, PA
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The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated:  12/31/1969
Advanced Wound Care Center at Yavapai Regional Medical Center
mi
from
Prescott Valley, AZ
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated: 12/31/1969
Advanced Wound Care Center at Yavapai Regional Medical Center
mi
from
Prescott Valley, AZ
Click here to add this to my saved trials
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated:  12/31/1969
Jupiter Medical Center
mi
from
Jupiter, FL
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated: 12/31/1969
Jupiter Medical Center
mi
from
Jupiter, FL
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The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated:  12/31/1969
West Gables Rehab Hospital
mi
from
Miami, FL
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated: 12/31/1969
West Gables Rehab Hospital
mi
from
Miami, FL
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The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated:  12/31/1969
Institute for Advanced Wound Healing; Northshore Specialty Hospital
mi
from
Covington, LA
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated: 12/31/1969
Institute for Advanced Wound Healing; Northshore Specialty Hospital
mi
from
Covington, LA
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The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated:  12/31/1969
Wound Care Associates, LLC.
mi
from
Hammond, LA
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated: 12/31/1969
Wound Care Associates, LLC.
mi
from
Hammond, LA
Click here to add this to my saved trials
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated:  12/31/1969
Opelousas General Hospital Wound Center
mi
from
Opelousas, LA
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated: 12/31/1969
Opelousas General Hospital Wound Center
mi
from
Opelousas, LA
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The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated:  12/31/1969
Saint Louis Foot and Ankle
mi
from
Saint Louis, MO
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated: 12/31/1969
Saint Louis Foot and Ankle
mi
from
Saint Louis, MO
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The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated:  12/31/1969
CentraState Medical Center
mi
from
Freehold, NJ
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated: 12/31/1969
CentraState Medical Center
mi
from
Freehold, NJ
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The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated:  12/31/1969
Robert Wood Johnson Hamilton
mi
from
Hamilton, NJ
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated: 12/31/1969
Robert Wood Johnson Hamilton
mi
from
Hamilton, NJ
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The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated:  12/31/1969
Southampton Hospital
mi
from
Southampton, NY
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated: 12/31/1969
Southampton Hospital
mi
from
Southampton, NY
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The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated:  12/31/1969
Wayne Memorial Hospital
mi
from
Goldsboro, NC
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated: 12/31/1969
Wayne Memorial Hospital
mi
from
Goldsboro, NC
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The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated:  12/31/1969
Sacred Heart Hospital
mi
from
Allentown, PA
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated: 12/31/1969
Sacred Heart Hospital
mi
from
Allentown, PA
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The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated:  12/31/1969
Harrisburg Foot and Ankle Center
mi
from
Harrisburg, PA
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated: 12/31/1969
Harrisburg Foot and Ankle Center
mi
from
Harrisburg, PA
Click here to add this to my saved trials
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated:  12/31/1969
Greensville Health System
mi
from
Greenville, SC
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated: 12/31/1969
Greensville Health System
mi
from
Greenville, SC
Click here to add this to my saved trials
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated:  12/31/1969
Meriter Hospital Inc., DBA: UnityPoint Health Heart and Vascular Institute
mi
from
Madison, WI
The RESPOND Registry
Real-World Effectiveness Study of PuraPly™ AM on Wounds
Status: Enrolling
Updated: 12/31/1969
Meriter Hospital Inc., DBA: UnityPoint Health Heart and Vascular Institute
mi
from
Madison, WI
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CAR-T Intraperitoneal Infusions for CEA-Expressing Adenocarcinoma Peritoneal Metastases or Malignant Ascites (IPC)
Immunotherapy for Peritoneal Carcinomatosis (IPC) - A Phase I Study of the Safety and Efficacy of Anti-CEA CAR-T Cell Intraperitoneal Infusions for Treatment of CEA-Expressing Adenocarcinoma Peritoneal Metastases or Malignant Ascites
Status: Enrolling
Updated:  12/31/1969
Rutgers Cancer Institute of New Jersey
mi
from
New Brunswick, NJ
CAR-T Intraperitoneal Infusions for CEA-Expressing Adenocarcinoma Peritoneal Metastases or Malignant Ascites (IPC)
Immunotherapy for Peritoneal Carcinomatosis (IPC) - A Phase I Study of the Safety and Efficacy of Anti-CEA CAR-T Cell Intraperitoneal Infusions for Treatment of CEA-Expressing Adenocarcinoma Peritoneal Metastases or Malignant Ascites
Status: Enrolling
Updated: 12/31/1969
Rutgers Cancer Institute of New Jersey
mi
from
New Brunswick, NJ
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CAR-T Intraperitoneal Infusions for CEA-Expressing Adenocarcinoma Peritoneal Metastases or Malignant Ascites (IPC)
Immunotherapy for Peritoneal Carcinomatosis (IPC) - A Phase I Study of the Safety and Efficacy of Anti-CEA CAR-T Cell Intraperitoneal Infusions for Treatment of CEA-Expressing Adenocarcinoma Peritoneal Metastases or Malignant Ascites
Status: Enrolling
Updated:  12/31/1969
Roger Williams Medical Center
mi
from
Providence, RI
CAR-T Intraperitoneal Infusions for CEA-Expressing Adenocarcinoma Peritoneal Metastases or Malignant Ascites (IPC)
Immunotherapy for Peritoneal Carcinomatosis (IPC) - A Phase I Study of the Safety and Efficacy of Anti-CEA CAR-T Cell Intraperitoneal Infusions for Treatment of CEA-Expressing Adenocarcinoma Peritoneal Metastases or Malignant Ascites
Status: Enrolling
Updated: 12/31/1969
Roger Williams Medical Center
mi
from
Providence, RI
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Evaluating the Combined Effect of Vedolizumab and Semi-Vegetarian Diet on Ulcerative Colitis.
A Pilot Study Evaluating the Synergistic Effect of Vedolizumab in Conjunction With Structured Semi-Vegetarian Diet on the Treatment of Ulcerative Colitis.
Status: Enrolling
Updated:  12/31/1969
Mayo Clinic Florida
mi
from
Jacksonville, FL
Evaluating the Combined Effect of Vedolizumab and Semi-Vegetarian Diet on Ulcerative Colitis.
A Pilot Study Evaluating the Synergistic Effect of Vedolizumab in Conjunction With Structured Semi-Vegetarian Diet on the Treatment of Ulcerative Colitis.
Status: Enrolling
Updated: 12/31/1969
Mayo Clinic Florida
mi
from
Jacksonville, FL
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Safety Evaluation of a Diet and Nutritional Supplementation Program- Purify 2.0
Safety Evaluation of a Diet and Nutritional Supplementation Program for Support of Balanced Bowel Function in Healthy Volunteers
Status: Enrolling
Updated:  12/31/1969
The Hughes Center for Research and Innovation
mi
from
Lehi, UT
Safety Evaluation of a Diet and Nutritional Supplementation Program- Purify 2.0
Safety Evaluation of a Diet and Nutritional Supplementation Program for Support of Balanced Bowel Function in Healthy Volunteers
Status: Enrolling
Updated: 12/31/1969
The Hughes Center for Research and Innovation
mi
from
Lehi, UT
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Transfusions and Nitric Oxide Level in Preterm Infants
Transfusions and Nitric Oxide Level in Preterm Infants
Status: Enrolling
Updated:  12/31/1969
Duke Univ Med Ctr
mi
from
Durham, NC
Transfusions and Nitric Oxide Level in Preterm Infants
Transfusions and Nitric Oxide Level in Preterm Infants
Status: Enrolling
Updated: 12/31/1969
Duke Univ Med Ctr
mi
from
Durham, NC
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BLI4700-202: A Pilot Evaluation of BLI4700 Bowel Preparation in Adult Subjects
A Pilot Evaluation of BLI4700 Bowel Preparation in Adult Subjects
Status: Enrolling
Updated:  12/31/1969
Braintree Research Site 11
mi
from
Anaheim, CA
BLI4700-202: A Pilot Evaluation of BLI4700 Bowel Preparation in Adult Subjects
A Pilot Evaluation of BLI4700 Bowel Preparation in Adult Subjects
Status: Enrolling
Updated: 12/31/1969
Braintree Research Site 11
mi
from
Anaheim, CA
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BLI4700-202: A Pilot Evaluation of BLI4700 Bowel Preparation in Adult Subjects
A Pilot Evaluation of BLI4700 Bowel Preparation in Adult Subjects
Status: Enrolling
Updated:  12/31/1969
Braintree Research Site 7
mi
from
Bastrop, LA
BLI4700-202: A Pilot Evaluation of BLI4700 Bowel Preparation in Adult Subjects
A Pilot Evaluation of BLI4700 Bowel Preparation in Adult Subjects
Status: Enrolling
Updated: 12/31/1969
Braintree Research Site 7
mi
from
Bastrop, LA
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Wearable Vibration Device to Prevent Bone Loss in Postmenopausal Women--Aim 2
Wearable Vibration Device to Prevent Bone Loss in Postmenopausal Women--Aim 2
Status: Enrolling
Updated:  12/31/1969
Univ of Nebraska Med Ctr
mi
from
Omaha, NE
Wearable Vibration Device to Prevent Bone Loss in Postmenopausal Women--Aim 2
Wearable Vibration Device to Prevent Bone Loss in Postmenopausal Women--Aim 2
Status: Enrolling
Updated: 12/31/1969
Univ of Nebraska Med Ctr
mi
from
Omaha, NE
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Effects of Potato Resistant Starch Intake on Insulin Sensitivity, Related Metabolic Markers and Satiety
Effects of Potato Resistant Starch Intake on Insulin Sensitivity, Related Metabolic Markers and Satiety in Men and Women at Risk for Type 2 Diabetes
Status: Enrolling
Updated:  12/31/1969
Cathy Maki
mi
from
Boca Raton, FL
Effects of Potato Resistant Starch Intake on Insulin Sensitivity, Related Metabolic Markers and Satiety
Effects of Potato Resistant Starch Intake on Insulin Sensitivity, Related Metabolic Markers and Satiety in Men and Women at Risk for Type 2 Diabetes
Status: Enrolling
Updated: 12/31/1969
Cathy Maki
mi
from
Boca Raton, FL
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The Effects of Naltrexone on Active Crohn's Disease
The Effects of Naltrexone in Active Crohn's Disease
Status: Enrolling
Updated:  12/31/1969
Penn State Hershey Medical Center
mi
from
Hershey, PA
The Effects of Naltrexone on Active Crohn's Disease
The Effects of Naltrexone in Active Crohn's Disease
Status: Enrolling
Updated: 12/31/1969
Penn State Hershey Medical Center
mi
from
Hershey, PA
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Pilot Study to Improve Therapeutic Outcomes for Dysphagia After Radiation Therapy
Pilot Study to Improve Therapeutic Outcomes for Dysphagia After Radiation Therapy
Status: Enrolling
Updated:  12/31/1969
UPMC
mi
from
Pittsburgh, PA
Pilot Study to Improve Therapeutic Outcomes for Dysphagia After Radiation Therapy
Pilot Study to Improve Therapeutic Outcomes for Dysphagia After Radiation Therapy
Status: Enrolling
Updated: 12/31/1969
UPMC
mi
from
Pittsburgh, PA
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Phase 2 Trial of TD 6424 (Telavancin) Versus Standard Therapy for Complicated Gram Positive Skin and Skin Structure Infections (Gram Positive cSSSI)
A Phase 2, Randomized, Double-Blind, Multinational Trial of Intravenous Telavancin Versus Standard Therapy for Treatment of Complicated Gram Positive Skin and Skin Structure Infections (Gram Positive cSSSI)
Status: Enrolling
Updated:  12/31/1969
eStudy Site, 3450 Bonita Road, Ste 201
mi
from
Chula Vista, CA
Phase 2 Trial of TD 6424 (Telavancin) Versus Standard Therapy for Complicated Gram Positive Skin and Skin Structure Infections (Gram Positive cSSSI)
A Phase 2, Randomized, Double-Blind, Multinational Trial of Intravenous Telavancin Versus Standard Therapy for Treatment of Complicated Gram Positive Skin and Skin Structure Infections (Gram Positive cSSSI)
Status: Enrolling
Updated: 12/31/1969
eStudy Site, 3450 Bonita Road, Ste 201
mi
from
Chula Vista, CA
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Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated:  12/31/1969
GSK Investigational Site
mi
from
Birmingham, AL
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated: 12/31/1969
GSK Investigational Site
mi
from
Birmingham, AL
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Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated:  12/31/1969
GSK Investigational Site
mi
from
Scottsdale, AZ
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated: 12/31/1969
GSK Investigational Site
mi
from
Scottsdale, AZ
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Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated:  12/31/1969
GSK Investigational Site
mi
from
Little Rock, AR
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated: 12/31/1969
GSK Investigational Site
mi
from
Little Rock, AR
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Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated:  12/31/1969
GSK Investigational Site
mi
from
Los Angeles, CA
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated: 12/31/1969
GSK Investigational Site
mi
from
Los Angeles, CA
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Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated:  12/31/1969
GSK Investigational Site
mi
from
San Diego, CA
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated: 12/31/1969
GSK Investigational Site
mi
from
San Diego, CA
Click here to add this to my saved trials
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated:  12/31/1969
GSK Investigational Site
mi
from
San Francisco, CA
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated: 12/31/1969
GSK Investigational Site
mi
from
San Francisco, CA
Click here to add this to my saved trials
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated:  12/31/1969
GSK Investigational Site
mi
from
Denver, CO
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated: 12/31/1969
GSK Investigational Site
mi
from
Denver, CO
Click here to add this to my saved trials
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated:  12/31/1969
GSK Investigational Site
mi
from
Washington,
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated: 12/31/1969
GSK Investigational Site
mi
from
Washington,
Click here to add this to my saved trials
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated:  12/31/1969
GSK Investigational Site
mi
from
Jacksonville, FL
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated: 12/31/1969
GSK Investigational Site
mi
from
Jacksonville, FL
Click here to add this to my saved trials
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated:  12/31/1969
GSK Investigational Site
mi
from
Miami, FL
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated: 12/31/1969
GSK Investigational Site
mi
from
Miami, FL
Click here to add this to my saved trials
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated:  12/31/1969
GSK Investigational Site
mi
from
Chicago, IL
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated: 12/31/1969
GSK Investigational Site
mi
from
Chicago, IL
Click here to add this to my saved trials
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated:  12/31/1969
GSK Investigational Site
mi
from
Indianapolis, IN
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated: 12/31/1969
GSK Investigational Site
mi
from
Indianapolis, IN
Click here to add this to my saved trials
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated:  12/31/1969
GSK Investigational Site
mi
from
New Orleans, LA
Eltrombopag To Reduce The Need For Platelet Transfusion In Subjects With Chronic Liver Disease And Thrombocytopenia Undergoing Elective Invasive Procedures
Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Study to Evaluate the Safety and Efficacy of Eltrombopag to Reduce the Need for Platelet Transfusion in Thrombocytopenic Subjects With Chronic Liver Disease Undergoing Elective Invasive Procedures
Status: Enrolling
Updated: 12/31/1969
GSK Investigational Site
mi
from
New Orleans, LA
Click here to add this to my saved trials