Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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

A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated:  12/18/2015
Clinical Research Facility
mi
from
Marrero, LA
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated: 12/18/2015
Clinical Research Facility
mi
from
Marrero, LA
Click here to add this to my saved trials
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated:  12/18/2015
Clinical Research Facility
mi
from
Shreveport, LA
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated: 12/18/2015
Clinical Research Facility
mi
from
Shreveport, LA
Click here to add this to my saved trials
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated:  12/18/2015
Clinical Research Facility
mi
from
Shreveport, LA
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated: 12/18/2015
Clinical Research Facility
mi
from
Shreveport, LA
Click here to add this to my saved trials
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated:  12/18/2015
Clinical Research Facility
mi
from
Farmington Hills, MI
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated: 12/18/2015
Clinical Research Facility
mi
from
Farmington Hills, MI
Click here to add this to my saved trials
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated:  12/18/2015
Clinical Research Facility
mi
from
Flat Rock, NC
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated: 12/18/2015
Clinical Research Facility
mi
from
Flat Rock, NC
Click here to add this to my saved trials
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated:  12/18/2015
Clinical Research Facility
mi
from
Cleveland, OH
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated: 12/18/2015
Clinical Research Facility
mi
from
Cleveland, OH
Click here to add this to my saved trials
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated:  12/18/2015
Clinical Research Facility
mi
from
Orem, UT
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated: 12/18/2015
Clinical Research Facility
mi
from
Orem, UT
Click here to add this to my saved trials
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated:  12/18/2015
Clinical Research Facility
mi
from
Falls Church, VA
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated: 12/18/2015
Clinical Research Facility
mi
from
Falls Church, VA
Click here to add this to my saved trials
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated:  12/18/2015
mi
from
Lille,
A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Cancer-Related Pain, Followed by an Open-Label Extension Phase
Status: Enrolling
Updated: 12/18/2015
mi
from
Lille,
Click here to add this to my saved trials
Safety, Tolerability and Effectiveness of Nuedexta in the Treatment of Pseudobulbar Affect (PBA)
A Study to Assess the Safety, Tolerability and Effectiveness of Nuedexta (Dextromethorphan 20 mg/Quinidine 10 mg) in the Treatment of Pseudobulbar Affect (PBA)
Status: Enrolling
Updated:  12/18/2015
Clinical Research Facility
mi
from
Pensacola, FL
Safety, Tolerability and Effectiveness of Nuedexta in the Treatment of Pseudobulbar Affect (PBA)
A Study to Assess the Safety, Tolerability and Effectiveness of Nuedexta (Dextromethorphan 20 mg/Quinidine 10 mg) in the Treatment of Pseudobulbar Affect (PBA)
Status: Enrolling
Updated: 12/18/2015
Clinical Research Facility
mi
from
Pensacola, FL
Click here to add this to my saved trials
Exercise Training in Depressed Traumatic Brain Injury Survivors
Exercise Training in Depressed Traumatic Brain Injury Survivors
Status: Enrolling
Updated:  12/18/2015
Virginia Commonwealth University
mi
from
Richmond, VA
Exercise Training in Depressed Traumatic Brain Injury Survivors
Exercise Training in Depressed Traumatic Brain Injury Survivors
Status: Enrolling
Updated: 12/18/2015
Virginia Commonwealth University
mi
from
Richmond, VA
Click here to add this to my saved trials
Pelvic CT Imaging in Blunt Abdominal Trauma
Pelvic CT Imaging in Blunt Trauma: Limiting Low Yield Radiation Exposure in Carefully Selected Adult and Pediatric Patients
Status: Enrolling
Updated:  12/21/2015
Carolinas Medical Center
mi
from
Charlotte, NC
Pelvic CT Imaging in Blunt Abdominal Trauma
Pelvic CT Imaging in Blunt Trauma: Limiting Low Yield Radiation Exposure in Carefully Selected Adult and Pediatric Patients
Status: Enrolling
Updated: 12/21/2015
Carolinas Medical Center
mi
from
Charlotte, NC
Click here to add this to my saved trials
Propofol Versus Alfentanil Versus Nitrous Oxide for Moderate Procedural Sedation
Propofol Versus Alfentanil Versus Nitrous Oxide for Moderate Procedural Sedation in the Emergency Department
Status: Enrolling
Updated:  12/22/2015
Hennepin County Medical Center
mi
from
Minneapolis, MN
Propofol Versus Alfentanil Versus Nitrous Oxide for Moderate Procedural Sedation
Propofol Versus Alfentanil Versus Nitrous Oxide for Moderate Procedural Sedation in the Emergency Department
Status: Enrolling
Updated: 12/22/2015
Hennepin County Medical Center
mi
from
Minneapolis, MN
Click here to add this to my saved trials
Stress Biomarkers Among Patients Undergoing Treatment for Excited Delirium and Severe Pain in the Emergency Department
Stress Biomarkers Among Patients Undergoing Treatment for Excited Delirium and Severe Pain in the Emergency Department
Status: Enrolling
Updated:  12/22/2015
Hennepin County Medical Center
mi
from
Minneapolis, MN
Stress Biomarkers Among Patients Undergoing Treatment for Excited Delirium and Severe Pain in the Emergency Department
Stress Biomarkers Among Patients Undergoing Treatment for Excited Delirium and Severe Pain in the Emergency Department
Status: Enrolling
Updated: 12/22/2015
Hennepin County Medical Center
mi
from
Minneapolis, MN
Click here to add this to my saved trials
Oscillatory Versus Non-Oscillatory Nasal Continuous Airway Pressure Neonatal Respiratory Support
Oscillatory Versus Non-Oscillatory Nasal Continuous Airway Pressure Neonatal Respiratory Support
Status: Enrolling
Updated:  12/23/2015
Valley Children's Healthcare
mi
from
Madera, CA
Oscillatory Versus Non-Oscillatory Nasal Continuous Airway Pressure Neonatal Respiratory Support
Oscillatory Versus Non-Oscillatory Nasal Continuous Airway Pressure Neonatal Respiratory Support
Status: Enrolling
Updated: 12/23/2015
Valley Children's Healthcare
mi
from
Madera, CA
Click here to add this to my saved trials
Oscillatory Versus Non-Oscillatory Nasal Continuous Airway Pressure Neonatal Respiratory Support
Oscillatory Versus Non-Oscillatory Nasal Continuous Airway Pressure Neonatal Respiratory Support
Status: Enrolling
Updated:  12/23/2015
Primary Children's Medical Center
mi
from
Salt Lake City, UT
Oscillatory Versus Non-Oscillatory Nasal Continuous Airway Pressure Neonatal Respiratory Support
Oscillatory Versus Non-Oscillatory Nasal Continuous Airway Pressure Neonatal Respiratory Support
Status: Enrolling
Updated: 12/23/2015
Primary Children's Medical Center
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Oscillatory Versus Non-Oscillatory Nasal Continuous Airway Pressure Neonatal Respiratory Support
Oscillatory Versus Non-Oscillatory Nasal Continuous Airway Pressure Neonatal Respiratory Support
Status: Enrolling
Updated:  12/23/2015
University of Utah Health Sciences Center
mi
from
Salt Lake City, UT
Oscillatory Versus Non-Oscillatory Nasal Continuous Airway Pressure Neonatal Respiratory Support
Oscillatory Versus Non-Oscillatory Nasal Continuous Airway Pressure Neonatal Respiratory Support
Status: Enrolling
Updated: 12/23/2015
University of Utah Health Sciences Center
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
A Randomized Controlled Trial of Lung Ultrasound Compared to Chest X-ray for Diagnosing Pneumonia in the Emergency Department
Comparative Effectiveness of Lung Ultrasound vs. Chest X-ray for the Diagnosis of Pneumonia in the Emergency Department
Status: Enrolling
Updated:  12/24/2015
Icahn School of Medicine at Mount Sinai
mi
from
New York, NY
A Randomized Controlled Trial of Lung Ultrasound Compared to Chest X-ray for Diagnosing Pneumonia in the Emergency Department
Comparative Effectiveness of Lung Ultrasound vs. Chest X-ray for the Diagnosis of Pneumonia in the Emergency Department
Status: Enrolling
Updated: 12/24/2015
Icahn School of Medicine at Mount Sinai
mi
from
New York, NY
Click here to add this to my saved trials
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated:  12/24/2015
Clinical Research Facility
mi
from
Laconia, NH
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated: 12/24/2015
Clinical Research Facility
mi
from
Laconia, NH
Click here to add this to my saved trials
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated:  12/24/2015
Clinical Research Facility
mi
from
Phoenix, AZ
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated: 12/24/2015
Clinical Research Facility
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated:  12/24/2015
Clinical Research Facility
mi
from
Sylmar, CA
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated: 12/24/2015
Clinical Research Facility
mi
from
Sylmar, CA
Click here to add this to my saved trials
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated:  12/24/2015
Clinical Research Facility
mi
from
DeLand, FL
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated: 12/24/2015
Clinical Research Facility
mi
from
DeLand, FL
Click here to add this to my saved trials
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated:  12/24/2015
Clinical Research Facility
mi
from
Chicago, IL
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated: 12/24/2015
Clinical Research Facility
mi
from
Chicago, IL
Click here to add this to my saved trials
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated:  12/24/2015
Clinical Research Facility
mi
from
Kansas City, KA
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated: 12/24/2015
Clinical Research Facility
mi
from
Kansas City, KA
Click here to add this to my saved trials
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated:  12/24/2015
Clinical Research Facility
mi
from
Royal Oak, MI
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated: 12/24/2015
Clinical Research Facility
mi
from
Royal Oak, MI
Click here to add this to my saved trials
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated:  12/24/2015
Clinical Research Facility
mi
from
Minneapolis, MN
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated: 12/24/2015
Clinical Research Facility
mi
from
Minneapolis, MN
Click here to add this to my saved trials
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated:  12/24/2015
Clinical Research Facility
mi
from
St. Louis, MO
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated: 12/24/2015
Clinical Research Facility
mi
from
St. Louis, MO
Click here to add this to my saved trials
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated:  12/24/2015
Clinical Research Facility
mi
from
Omaha, NE
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated: 12/24/2015
Clinical Research Facility
mi
from
Omaha, NE
Click here to add this to my saved trials
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated:  12/24/2015
Clinical Research Facility
mi
from
Columbus, OH
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated: 12/24/2015
Clinical Research Facility
mi
from
Columbus, OH
Click here to add this to my saved trials
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated:  12/24/2015
Clinical Research Facility
mi
from
Lima, OH
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated: 12/24/2015
Clinical Research Facility
mi
from
Lima, OH
Click here to add this to my saved trials
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated:  12/24/2015
Clinical Research Facility
mi
from
Oklahoma City, OK
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated: 12/24/2015
Clinical Research Facility
mi
from
Oklahoma City, OK
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Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated:  12/24/2015
Investigational Site
mi
from
Tbilisi,
Evaluation of Ceftaroline Fosamil Versus a Comparator in Adult Subjects With Community-acquired Bacterial Pneumonia (CABP) With Risk for Methicillin-resistant Staphylococcus Aureus
A Multicenter, Multinational, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of Ceftaroline Fosamil Versus Ceftriaxone Plus Vancomycin in Adult Subjects With Community-acquired Bacterial Pneumonia at Risk for Infection Due to Methicillin-resistant Staphylococcus Aureus
Status: Enrolling
Updated: 12/24/2015
Investigational Site
mi
from
Tbilisi,
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Pilot Study of Fosamax in Spinal Cord Injury
Double Blind Placebo Controlled Trial to Evaluate Preservation of Bone Mineral Density of the Hip and Distal Femur by Biphosphate Therapy (Fosamax) Following Spinal Cord Injury
Status: Enrolling
Updated:  12/25/2015
University of Rochester
mi
from
Rochester, NY
Pilot Study of Fosamax in Spinal Cord Injury
Double Blind Placebo Controlled Trial to Evaluate Preservation of Bone Mineral Density of the Hip and Distal Femur by Biphosphate Therapy (Fosamax) Following Spinal Cord Injury
Status: Enrolling
Updated: 12/25/2015
University of Rochester
mi
from
Rochester, NY
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Pilot Study of Fosamax in Spinal Cord Injury
Double Blind Placebo Controlled Trial to Evaluate Preservation of Bone Mineral Density of the Hip and Distal Femur by Biphosphate Therapy (Fosamax) Following Spinal Cord Injury
Status: Enrolling
Updated:  12/25/2015
University of Rochester Physical Medicine and Rehabilitation
mi
from
Rochester, NY
Pilot Study of Fosamax in Spinal Cord Injury
Double Blind Placebo Controlled Trial to Evaluate Preservation of Bone Mineral Density of the Hip and Distal Femur by Biphosphate Therapy (Fosamax) Following Spinal Cord Injury
Status: Enrolling
Updated: 12/25/2015
University of Rochester Physical Medicine and Rehabilitation
mi
from
Rochester, NY
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Procurement of Human Specimens for the Evaluation of Early Markers of Sepsis
Observational Study to Procure Human Specimens for Use in the Diagnosis and Management of Sepsis and Other Related Conditions
Status: Enrolling
Updated:  12/28/2015
Emory University Hospital
mi
from
Atlanta, GA
Procurement of Human Specimens for the Evaluation of Early Markers of Sepsis
Observational Study to Procure Human Specimens for Use in the Diagnosis and Management of Sepsis and Other Related Conditions
Status: Enrolling
Updated: 12/28/2015
Emory University Hospital
mi
from
Atlanta, GA
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Procurement of Human Specimens for the Evaluation of Early Markers of Sepsis
Observational Study to Procure Human Specimens for Use in the Diagnosis and Management of Sepsis and Other Related Conditions
Status: Enrolling
Updated:  12/28/2015
Grady Memorial Hospital
mi
from
Atlanta, GA
Procurement of Human Specimens for the Evaluation of Early Markers of Sepsis
Observational Study to Procure Human Specimens for Use in the Diagnosis and Management of Sepsis and Other Related Conditions
Status: Enrolling
Updated: 12/28/2015
Grady Memorial Hospital
mi
from
Atlanta, GA
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Study of a New Clinical Device for Reducing Body Core Temperature
Study of a New Clinical Device for Reducing Body Core Temperature
Status: Enrolling
Updated:  12/29/2015
Seton Medical Center
mi
from
Austin, TX
Study of a New Clinical Device for Reducing Body Core Temperature
Study of a New Clinical Device for Reducing Body Core Temperature
Status: Enrolling
Updated: 12/29/2015
Seton Medical Center
mi
from
Austin, TX
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Study of a New Clinical Device for Reducing Body Core Temperature
Study of a New Clinical Device for Reducing Body Core Temperature
Status: Enrolling
Updated:  12/29/2015
University Medical Center Brackenridge
mi
from
Austin, TX
Study of a New Clinical Device for Reducing Body Core Temperature
Study of a New Clinical Device for Reducing Body Core Temperature
Status: Enrolling
Updated: 12/29/2015
University Medical Center Brackenridge
mi
from
Austin, TX
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Treatment of Crohn's Fistula Using a Porcine Intestine Submucosa Graft
Treatment of Crohn's Fistula Using a Porcine Intestine Submucosa Graft (SurgiSIS AFP)
Status: Enrolling
Updated:  12/29/2015
Cedars-Sinai Medical Center
mi
from
Los Angeles, CA
Treatment of Crohn's Fistula Using a Porcine Intestine Submucosa Graft
Treatment of Crohn's Fistula Using a Porcine Intestine Submucosa Graft (SurgiSIS AFP)
Status: Enrolling
Updated: 12/29/2015
Cedars-Sinai Medical Center
mi
from
Los Angeles, CA
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Treatment of Crohn's Fistula Using a Porcine Intestine Submucosa Graft
Treatment of Crohn's Fistula Using a Porcine Intestine Submucosa Graft (SurgiSIS AFP)
Status: Enrolling
Updated:  12/29/2015
Mount Sinai Hospital
mi
from
New York, NY
Treatment of Crohn's Fistula Using a Porcine Intestine Submucosa Graft
Treatment of Crohn's Fistula Using a Porcine Intestine Submucosa Graft (SurgiSIS AFP)
Status: Enrolling
Updated: 12/29/2015
Mount Sinai Hospital
mi
from
New York, NY
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Treatment of Crohn's Fistula Using a Porcine Intestine Submucosa Graft
Treatment of Crohn's Fistula Using a Porcine Intestine Submucosa Graft (SurgiSIS AFP)
Status: Enrolling
Updated:  12/29/2015
Univeristy Hospitals Medical Center
mi
from
Cleveland, OH
Treatment of Crohn's Fistula Using a Porcine Intestine Submucosa Graft
Treatment of Crohn's Fistula Using a Porcine Intestine Submucosa Graft (SurgiSIS AFP)
Status: Enrolling
Updated: 12/29/2015
Univeristy Hospitals Medical Center
mi
from
Cleveland, OH
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Sildenafil for Cerebrovascular Dysfunction in Chronic Traumatic Brain Injury.
Sildenafil for the Treatment of Cerebrovascular Dysfunction During the Chronic Stage After Traumatic Brain Injury.
Status: Enrolling
Updated:  12/30/2015
National Institute of Health
mi
from
Bethesda, MD
Sildenafil for Cerebrovascular Dysfunction in Chronic Traumatic Brain Injury.
Sildenafil for the Treatment of Cerebrovascular Dysfunction During the Chronic Stage After Traumatic Brain Injury.
Status: Enrolling
Updated: 12/30/2015
National Institute of Health
mi
from
Bethesda, MD
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Does Cricoid Pressure Reduce the Risk of Aspiration?
Does Cricoid Pressure Reduce the Risk of Aspiration?
Status: Enrolling
Updated:  12/30/2015
Mayo Clinic Rochester
mi
from
Rochester, MN
Does Cricoid Pressure Reduce the Risk of Aspiration?
Does Cricoid Pressure Reduce the Risk of Aspiration?
Status: Enrolling
Updated: 12/30/2015
Mayo Clinic Rochester
mi
from
Rochester, MN
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Does Cricoid Pressure Reduce the Risk of Aspiration?
Does Cricoid Pressure Reduce the Risk of Aspiration?
Status: Enrolling
Updated:  12/30/2015
Mayo Clinic - Saint Mary's Campus
mi
from
Rochester, MN
Does Cricoid Pressure Reduce the Risk of Aspiration?
Does Cricoid Pressure Reduce the Risk of Aspiration?
Status: Enrolling
Updated: 12/30/2015
Mayo Clinic - Saint Mary's Campus
mi
from
Rochester, MN
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A Safety and Efficacy Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Multiple-Dose Efficacy and Safety Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Status: Enrolling
Updated:  12/30/2015
Clinical Research Facility
mi
from
Downey, CA
A Safety and Efficacy Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Multiple-Dose Efficacy and Safety Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Status: Enrolling
Updated: 12/30/2015
Clinical Research Facility
mi
from
Downey, CA
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A Safety and Efficacy Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Multiple-Dose Efficacy and Safety Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Status: Enrolling
Updated:  12/30/2015
Clinical Research Facility
mi
from
Gilroy, CA
A Safety and Efficacy Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Multiple-Dose Efficacy and Safety Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Status: Enrolling
Updated: 12/30/2015
Clinical Research Facility
mi
from
Gilroy, CA
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A Safety and Efficacy Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Multiple-Dose Efficacy and Safety Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Status: Enrolling
Updated:  12/30/2015
Clinical Research Facility
mi
from
Pasadena, CA
A Safety and Efficacy Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Multiple-Dose Efficacy and Safety Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Status: Enrolling
Updated: 12/30/2015
Clinical Research Facility
mi
from
Pasadena, CA
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A Safety and Efficacy Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Multiple-Dose Efficacy and Safety Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Status: Enrolling
Updated:  12/30/2015
Clinical Research Facility
mi
from
San Jose, CA
A Safety and Efficacy Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Multiple-Dose Efficacy and Safety Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Status: Enrolling
Updated: 12/30/2015
Clinical Research Facility
mi
from
San Jose, CA
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A Safety and Efficacy Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Multiple-Dose Efficacy and Safety Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Status: Enrolling
Updated:  12/30/2015
Clinical Research Facility
mi
from
Englewood, CO
A Safety and Efficacy Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Multiple-Dose Efficacy and Safety Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Status: Enrolling
Updated: 12/30/2015
Clinical Research Facility
mi
from
Englewood, CO
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A Safety and Efficacy Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Multiple-Dose Efficacy and Safety Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Status: Enrolling
Updated:  12/30/2015
Clinical Research Facility
mi
from
Miami, FL
A Safety and Efficacy Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Multiple-Dose Efficacy and Safety Study of XP19986 in Subjects With Spasticity Due to Spinal Cord Injury
Status: Enrolling
Updated: 12/30/2015
Clinical Research Facility
mi
from
Miami, FL
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