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
15,024
archived clinical trials in
Infectious Disease

MeFirst: A Tailored Intervention to HPV Vaccine Decision Making
MeFirst: A Tailored Intervention to HPV Vaccine Decision Making
Status: Enrolling
Updated:  7/21/2015
Univeristy of Michigan
mi
from
Ann Arbor, MI
MeFirst: A Tailored Intervention to HPV Vaccine Decision Making
MeFirst: A Tailored Intervention to HPV Vaccine Decision Making
Status: Enrolling
Updated: 7/21/2015
Univeristy of Michigan
mi
from
Ann Arbor, MI
Click here to add this to my saved trials
Efficacy of Combination Therapies for Gonorrhea Treatment
Randomized Clinical Trial Evaluating the Efficacy of Gentamicin/Azithromycin and Gemifloxacin/Azithromycin Combination Therapies as an Alternative Regimen for Uncomplicated Urogenital Gonorrhea
Status: Enrolling
Updated:  7/23/2015
University of Alabama Hospital - Infectious Diseases
mi
from
Birmingham, AL
Efficacy of Combination Therapies for Gonorrhea Treatment
Randomized Clinical Trial Evaluating the Efficacy of Gentamicin/Azithromycin and Gemifloxacin/Azithromycin Combination Therapies as an Alternative Regimen for Uncomplicated Urogenital Gonorrhea
Status: Enrolling
Updated: 7/23/2015
University of Alabama Hospital - Infectious Diseases
mi
from
Birmingham, AL
Click here to add this to my saved trials
Efficacy of Combination Therapies for Gonorrhea Treatment
Randomized Clinical Trial Evaluating the Efficacy of Gentamicin/Azithromycin and Gemifloxacin/Azithromycin Combination Therapies as an Alternative Regimen for Uncomplicated Urogenital Gonorrhea
Status: Enrolling
Updated:  7/23/2015
Los Angeles County Department of Public Health - Sexually Transmitted Disease Program
mi
from
Los Angeles, CA
Efficacy of Combination Therapies for Gonorrhea Treatment
Randomized Clinical Trial Evaluating the Efficacy of Gentamicin/Azithromycin and Gemifloxacin/Azithromycin Combination Therapies as an Alternative Regimen for Uncomplicated Urogenital Gonorrhea
Status: Enrolling
Updated: 7/23/2015
Los Angeles County Department of Public Health - Sexually Transmitted Disease Program
mi
from
Los Angeles, CA
Click here to add this to my saved trials
Efficacy of Combination Therapies for Gonorrhea Treatment
Randomized Clinical Trial Evaluating the Efficacy of Gentamicin/Azithromycin and Gemifloxacin/Azithromycin Combination Therapies as an Alternative Regimen for Uncomplicated Urogenital Gonorrhea
Status: Enrolling
Updated:  7/23/2015
San Francisco Department of Public Health - San Francisco City Clinic
mi
from
San Francisco, CA
Efficacy of Combination Therapies for Gonorrhea Treatment
Randomized Clinical Trial Evaluating the Efficacy of Gentamicin/Azithromycin and Gemifloxacin/Azithromycin Combination Therapies as an Alternative Regimen for Uncomplicated Urogenital Gonorrhea
Status: Enrolling
Updated: 7/23/2015
San Francisco Department of Public Health - San Francisco City Clinic
mi
from
San Francisco, CA
Click here to add this to my saved trials
Efficacy of Combination Therapies for Gonorrhea Treatment
Randomized Clinical Trial Evaluating the Efficacy of Gentamicin/Azithromycin and Gemifloxacin/Azithromycin Combination Therapies as an Alternative Regimen for Uncomplicated Urogenital Gonorrhea
Status: Enrolling
Updated:  7/23/2015
Johns Hopkins Bayview Medical Center - Infectious Diseases
mi
from
Baltimore, MD
Efficacy of Combination Therapies for Gonorrhea Treatment
Randomized Clinical Trial Evaluating the Efficacy of Gentamicin/Azithromycin and Gemifloxacin/Azithromycin Combination Therapies as an Alternative Regimen for Uncomplicated Urogenital Gonorrhea
Status: Enrolling
Updated: 7/23/2015
Johns Hopkins Bayview Medical Center - Infectious Diseases
mi
from
Baltimore, MD
Click here to add this to my saved trials
Efficacy of Combination Therapies for Gonorrhea Treatment
Randomized Clinical Trial Evaluating the Efficacy of Gentamicin/Azithromycin and Gemifloxacin/Azithromycin Combination Therapies as an Alternative Regimen for Uncomplicated Urogenital Gonorrhea
Status: Enrolling
Updated:  7/23/2015
Magee Women's Hospital of UPMC - Reproductive Infectious Disease Research
mi
from
Pittsburgh, PA
Efficacy of Combination Therapies for Gonorrhea Treatment
Randomized Clinical Trial Evaluating the Efficacy of Gentamicin/Azithromycin and Gemifloxacin/Azithromycin Combination Therapies as an Alternative Regimen for Uncomplicated Urogenital Gonorrhea
Status: Enrolling
Updated: 7/23/2015
Magee Women's Hospital of UPMC - Reproductive Infectious Disease Research
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
Evaluation of Accuracy and Ease of Use of the FilmArray™ Respiratory Panel (RP EZ) in a CLIA-Waived Clinical Setting
Evaluation of Accuracy and Ease of Use of the FilmArray™ Respiratory Panel (RP EZ) in a CLIA-Waived Clinical Setting
Status: Enrolling
Updated:  7/23/2015
Naval Health Research Center
mi
from
San Diego, CA
Evaluation of Accuracy and Ease of Use of the FilmArray™ Respiratory Panel (RP EZ) in a CLIA-Waived Clinical Setting
Evaluation of Accuracy and Ease of Use of the FilmArray™ Respiratory Panel (RP EZ) in a CLIA-Waived Clinical Setting
Status: Enrolling
Updated: 7/23/2015
Naval Health Research Center
mi
from
San Diego, CA
Click here to add this to my saved trials
Evaluation of Accuracy and Ease of Use of the FilmArray™ Respiratory Panel (RP EZ) in a CLIA-Waived Clinical Setting
Evaluation of Accuracy and Ease of Use of the FilmArray™ Respiratory Panel (RP EZ) in a CLIA-Waived Clinical Setting
Status: Enrolling
Updated:  7/23/2015
UTMB Primary Care Pavilion
mi
from
Galveston, TX
Evaluation of Accuracy and Ease of Use of the FilmArray™ Respiratory Panel (RP EZ) in a CLIA-Waived Clinical Setting
Evaluation of Accuracy and Ease of Use of the FilmArray™ Respiratory Panel (RP EZ) in a CLIA-Waived Clinical Setting
Status: Enrolling
Updated: 7/23/2015
UTMB Primary Care Pavilion
mi
from
Galveston, TX
Click here to add this to my saved trials
Evaluation of Accuracy and Ease of Use of the FilmArray™ Respiratory Panel (RP EZ) in a CLIA-Waived Clinical Setting
Evaluation of Accuracy and Ease of Use of the FilmArray™ Respiratory Panel (RP EZ) in a CLIA-Waived Clinical Setting
Status: Enrolling
Updated:  7/23/2015
South Main Clinic
mi
from
Salt Lake City, UT
Evaluation of Accuracy and Ease of Use of the FilmArray™ Respiratory Panel (RP EZ) in a CLIA-Waived Clinical Setting
Evaluation of Accuracy and Ease of Use of the FilmArray™ Respiratory Panel (RP EZ) in a CLIA-Waived Clinical Setting
Status: Enrolling
Updated: 7/23/2015
South Main Clinic
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Evaluation of Accuracy and Ease of Use of the FilmArray™ Respiratory Panel (RP EZ) in a CLIA-Waived Clinical Setting
Evaluation of Accuracy and Ease of Use of the FilmArray™ Respiratory Panel (RP EZ) in a CLIA-Waived Clinical Setting
Status: Enrolling
Updated:  7/23/2015
Barnes-Jewish/Washington University School of Medicine
mi
from
St. Louis, MO
Evaluation of Accuracy and Ease of Use of the FilmArray™ Respiratory Panel (RP EZ) in a CLIA-Waived Clinical Setting
Evaluation of Accuracy and Ease of Use of the FilmArray™ Respiratory Panel (RP EZ) in a CLIA-Waived Clinical Setting
Status: Enrolling
Updated: 7/23/2015
Barnes-Jewish/Washington University School of Medicine
mi
from
St. Louis, MO
Click here to add this to my saved trials
Enteral Glutamine in Reducing Bloodstream Infections in Short Bowel Syndrome Infants
Efficacy of Enteral Glutamine in Reducing Bloodstream Infections in Short Bowel Syndrome Infants
Status: Enrolling
Updated:  7/28/2015
C.S. Mott Children's Hosptial
mi
from
Ann Arbor, MI
Enteral Glutamine in Reducing Bloodstream Infections in Short Bowel Syndrome Infants
Efficacy of Enteral Glutamine in Reducing Bloodstream Infections in Short Bowel Syndrome Infants
Status: Enrolling
Updated: 7/28/2015
C.S. Mott Children's Hosptial
mi
from
Ann Arbor, MI
Click here to add this to my saved trials
Enteral Glutamine in Reducing Bloodstream Infections in Short Bowel Syndrome Infants
Efficacy of Enteral Glutamine in Reducing Bloodstream Infections in Short Bowel Syndrome Infants
Status: Enrolling
Updated:  7/28/2015
Cincinnati Children's Hospital Medical Center
mi
from
Cincinnati, OH
Enteral Glutamine in Reducing Bloodstream Infections in Short Bowel Syndrome Infants
Efficacy of Enteral Glutamine in Reducing Bloodstream Infections in Short Bowel Syndrome Infants
Status: Enrolling
Updated: 7/28/2015
Cincinnati Children's Hospital Medical Center
mi
from
Cincinnati, OH
Click here to add this to my saved trials
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Status: Enrolling
Updated:  7/28/2015
Denver Infectious Disease Consultants, PLLC
mi
from
Denver, CO
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Status: Enrolling
Updated: 7/28/2015
Denver Infectious Disease Consultants, PLLC
mi
from
Denver, CO
Click here to add this to my saved trials
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Status: Enrolling
Updated:  7/28/2015
University of Colorado Health Sciences Center
mi
from
Denver, CO
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Status: Enrolling
Updated: 7/28/2015
University of Colorado Health Sciences Center
mi
from
Denver, CO
Click here to add this to my saved trials
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Status: Enrolling
Updated:  7/28/2015
Hennepin County Medical Center
mi
from
Minneapolis, MN
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Status: Enrolling
Updated: 7/28/2015
Hennepin County Medical Center
mi
from
Minneapolis, MN
Click here to add this to my saved trials
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Status: Enrolling
Updated:  7/28/2015
Abbott Northwestern Hospital
mi
from
Minneapolis, MN
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Status: Enrolling
Updated: 7/28/2015
Abbott Northwestern Hospital
mi
from
Minneapolis, MN
Click here to add this to my saved trials
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Status: Enrolling
Updated:  7/28/2015
Park Nicollet Institute
mi
from
Minneapolis, MN
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Status: Enrolling
Updated: 7/28/2015
Park Nicollet Institute
mi
from
Minneapolis, MN
Click here to add this to my saved trials
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Status: Enrolling
Updated:  7/28/2015
Washington University School of Medicine
mi
from
St. Louis, MO
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Status: Enrolling
Updated: 7/28/2015
Washington University School of Medicine
mi
from
St. Louis, MO
Click here to add this to my saved trials
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Status: Enrolling
Updated:  7/28/2015
Miriam Hospital
mi
from
Providence, RI
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Status: Enrolling
Updated: 7/28/2015
Miriam Hospital
mi
from
Providence, RI
Click here to add this to my saved trials
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Status: Enrolling
Updated:  7/28/2015
Cerner Corporation
mi
from
McLean, VA
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study)
Status: Enrolling
Updated: 7/28/2015
Cerner Corporation
mi
from
McLean, VA
Click here to add this to my saved trials
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated:  7/30/2015
Denver Public Health Department
mi
from
Denver, CO
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated: 7/30/2015
Denver Public Health Department
mi
from
Denver, CO
Click here to add this to my saved trials
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated:  7/30/2015
Washington DC Veterans Affairs Medical Center
mi
from
Washington,
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated: 7/30/2015
Washington DC Veterans Affairs Medical Center
mi
from
Washington,
Click here to add this to my saved trials
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated:  7/30/2015
Duke University
mi
from
Durham, NC
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated: 7/30/2015
Duke University
mi
from
Durham, NC
Click here to add this to my saved trials
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated:  7/30/2015
Vanderbilt University Medical Center and Nashville Metro Public Health Department
mi
from
Nashville, TN
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated: 7/30/2015
Vanderbilt University Medical Center and Nashville Metro Public Health Department
mi
from
Nashville, TN
Click here to add this to my saved trials
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated:  7/30/2015
University of North Texas Health Science Center at Fort Worth
mi
from
Fort Worth, TX
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated: 7/30/2015
University of North Texas Health Science Center at Fort Worth
mi
from
Fort Worth, TX
Click here to add this to my saved trials
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated:  7/30/2015
South Texas - Department of State Health Services
mi
from
San Antonio, TX
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated: 7/30/2015
South Texas - Department of State Health Services
mi
from
San Antonio, TX
Click here to add this to my saved trials
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated:  7/30/2015
Audie L. Murphy VA Hospital
mi
from
San Antonio, TX
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated: 7/30/2015
Audie L. Murphy VA Hospital
mi
from
San Antonio, TX
Click here to add this to my saved trials
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated:  7/30/2015
University of California at San Francisco
mi
from
San Francisco, CA
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated: 7/30/2015
University of California at San Francisco
mi
from
San Francisco, CA
Click here to add this to my saved trials
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated:  7/30/2015
Columbia University College of Physicians and Surgeons and New York City Department of Health
mi
from
New York, NY
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated: 7/30/2015
Columbia University College of Physicians and Surgeons and New York City Department of Health
mi
from
New York, NY
Click here to add this to my saved trials
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated:  7/30/2015
TB and Chest service of Hong Kong
mi
from
Hong Kong,
Study 33: Adherence to Latent Tuberculosis Infection Treatment 3HP SAT Versus 3HP DOT
TBTC Study 33. An Evaluation of Adherence to Latent Tuberculosis Infection (LTBI) Treatment With 12 Doses of Once Weekly Rifapentine (RPT) and Isoniazid (INH) Given as Self-administered (SAT) Versus Directly-observed Therapy (DOT): iAdhere.
Status: Enrolling
Updated: 7/30/2015
TB and Chest service of Hong Kong
mi
from
Hong Kong,
Click here to add this to my saved trials
Efficacy of Micro-Patterned Foley Catheter to Reduce Catheter-Associated Urinary Tract Infection
Clinical Study to Assess the Efficacy of a Novel Micro-Patterned Foley Catheter to Reduce Catheter-Associated UrinaryTract Infection Among Spinal Cord Injury Patients
Status: Enrolling
Updated:  7/30/2015
James A. Haley Veterans Hospital
mi
from
Tampa, FL
Efficacy of Micro-Patterned Foley Catheter to Reduce Catheter-Associated Urinary Tract Infection
Clinical Study to Assess the Efficacy of a Novel Micro-Patterned Foley Catheter to Reduce Catheter-Associated UrinaryTract Infection Among Spinal Cord Injury Patients
Status: Enrolling
Updated: 7/30/2015
James A. Haley Veterans Hospital
mi
from
Tampa, FL
Click here to add this to my saved trials
Efficacy of Micro-Patterned Foley Catheter to Reduce Catheter-Associated Urinary Tract Infection
Clinical Study to Assess the Efficacy of a Novel Micro-Patterned Foley Catheter to Reduce Catheter-Associated UrinaryTract Infection Among Spinal Cord Injury Patients
Status: Enrolling
Updated:  7/30/2015
Michael E. DeBakey Veterans Affairs Medical Center
mi
from
Houston, TX
Efficacy of Micro-Patterned Foley Catheter to Reduce Catheter-Associated Urinary Tract Infection
Clinical Study to Assess the Efficacy of a Novel Micro-Patterned Foley Catheter to Reduce Catheter-Associated UrinaryTract Infection Among Spinal Cord Injury Patients
Status: Enrolling
Updated: 7/30/2015
Michael E. DeBakey Veterans Affairs Medical Center
mi
from
Houston, TX
Click here to add this to my saved trials
Study to Compare TP-434 and Ertapenem in Community-acquired Complicated Intra-abdominal Infections
A Phase 2, Randomized, Double-Blind, Double-Dummy, Multicenter, Prospective Study to Assess the Efficacy, Safety, and PK of 2 Dose Regimens of TP-434 Compared With Ertapenem in Adult Community-Acquired Complicated Intra-abdominal Infections
Status: Enrolling
Updated:  8/4/2015
Mercury Street Medical Group, Pllc
mi
from
Butte, MT
Study to Compare TP-434 and Ertapenem in Community-acquired Complicated Intra-abdominal Infections
A Phase 2, Randomized, Double-Blind, Double-Dummy, Multicenter, Prospective Study to Assess the Efficacy, Safety, and PK of 2 Dose Regimens of TP-434 Compared With Ertapenem in Adult Community-Acquired Complicated Intra-abdominal Infections
Status: Enrolling
Updated: 8/4/2015
Mercury Street Medical Group, Pllc
mi
from
Butte, MT
Click here to add this to my saved trials
Study to Compare TP-434 and Ertapenem in Community-acquired Complicated Intra-abdominal Infections
A Phase 2, Randomized, Double-Blind, Double-Dummy, Multicenter, Prospective Study to Assess the Efficacy, Safety, and PK of 2 Dose Regimens of TP-434 Compared With Ertapenem in Adult Community-Acquired Complicated Intra-abdominal Infections
Status: Enrolling
Updated:  8/4/2015
Long Beach VA Medical Center
mi
from
Long Beach, CA
Study to Compare TP-434 and Ertapenem in Community-acquired Complicated Intra-abdominal Infections
A Phase 2, Randomized, Double-Blind, Double-Dummy, Multicenter, Prospective Study to Assess the Efficacy, Safety, and PK of 2 Dose Regimens of TP-434 Compared With Ertapenem in Adult Community-Acquired Complicated Intra-abdominal Infections
Status: Enrolling
Updated: 8/4/2015
Long Beach VA Medical Center
mi
from
Long Beach, CA
Click here to add this to my saved trials
Study to Compare TP-434 and Ertapenem in Community-acquired Complicated Intra-abdominal Infections
A Phase 2, Randomized, Double-Blind, Double-Dummy, Multicenter, Prospective Study to Assess the Efficacy, Safety, and PK of 2 Dose Regimens of TP-434 Compared With Ertapenem in Adult Community-Acquired Complicated Intra-abdominal Infections
Status: Enrolling
Updated:  8/4/2015
Denver Health Medical Center
mi
from
Denver, CO
Study to Compare TP-434 and Ertapenem in Community-acquired Complicated Intra-abdominal Infections
A Phase 2, Randomized, Double-Blind, Double-Dummy, Multicenter, Prospective Study to Assess the Efficacy, Safety, and PK of 2 Dose Regimens of TP-434 Compared With Ertapenem in Adult Community-Acquired Complicated Intra-abdominal Infections
Status: Enrolling
Updated: 8/4/2015
Denver Health Medical Center
mi
from
Denver, CO
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Study to Compare TP-434 and Ertapenem in Community-acquired Complicated Intra-abdominal Infections
A Phase 2, Randomized, Double-Blind, Double-Dummy, Multicenter, Prospective Study to Assess the Efficacy, Safety, and PK of 2 Dose Regimens of TP-434 Compared With Ertapenem in Adult Community-Acquired Complicated Intra-abdominal Infections
Status: Enrolling
Updated:  8/4/2015
Henry Ford Hospital
mi
from
Detroit, MI
Study to Compare TP-434 and Ertapenem in Community-acquired Complicated Intra-abdominal Infections
A Phase 2, Randomized, Double-Blind, Double-Dummy, Multicenter, Prospective Study to Assess the Efficacy, Safety, and PK of 2 Dose Regimens of TP-434 Compared With Ertapenem in Adult Community-Acquired Complicated Intra-abdominal Infections
Status: Enrolling
Updated: 8/4/2015
Henry Ford Hospital
mi
from
Detroit, MI
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Study to Compare TP-434 and Ertapenem in Community-acquired Complicated Intra-abdominal Infections
A Phase 2, Randomized, Double-Blind, Double-Dummy, Multicenter, Prospective Study to Assess the Efficacy, Safety, and PK of 2 Dose Regimens of TP-434 Compared With Ertapenem in Adult Community-Acquired Complicated Intra-abdominal Infections
Status: Enrolling
Updated:  8/4/2015
Barnes Jewish Hospital
mi
from
St. Louis, MO
Study to Compare TP-434 and Ertapenem in Community-acquired Complicated Intra-abdominal Infections
A Phase 2, Randomized, Double-Blind, Double-Dummy, Multicenter, Prospective Study to Assess the Efficacy, Safety, and PK of 2 Dose Regimens of TP-434 Compared With Ertapenem in Adult Community-Acquired Complicated Intra-abdominal Infections
Status: Enrolling
Updated: 8/4/2015
Barnes Jewish Hospital
mi
from
St. Louis, MO
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Study to Compare TP-434 and Ertapenem in Community-acquired Complicated Intra-abdominal Infections
A Phase 2, Randomized, Double-Blind, Double-Dummy, Multicenter, Prospective Study to Assess the Efficacy, Safety, and PK of 2 Dose Regimens of TP-434 Compared With Ertapenem in Adult Community-Acquired Complicated Intra-abdominal Infections
Status: Enrolling
Updated:  8/4/2015
MHAT "Yulia Vrevska - Byala" EOOD, Byala
mi
from
Byala,
Study to Compare TP-434 and Ertapenem in Community-acquired Complicated Intra-abdominal Infections
A Phase 2, Randomized, Double-Blind, Double-Dummy, Multicenter, Prospective Study to Assess the Efficacy, Safety, and PK of 2 Dose Regimens of TP-434 Compared With Ertapenem in Adult Community-Acquired Complicated Intra-abdominal Infections
Status: Enrolling
Updated: 8/4/2015
MHAT "Yulia Vrevska - Byala" EOOD, Byala
mi
from
Byala,
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Cyclophosphamide for Prevention of Graft-Versus-Host Disease After Allogeneic Peripheral Blood Stem Cell Transplantation in Patients With Hematological Malignancies
A Phase II Study to Evaluate the Efficacy of Posttransplant Cyclophosphamide for Prevention of Chronic Graft-versus-Host Disease After Allogeneic Peripheral Blood Stem Cell Transplantation
Status: Enrolling
Updated:  8/4/2015
Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium
mi
from
Seattle, WA
Cyclophosphamide for Prevention of Graft-Versus-Host Disease After Allogeneic Peripheral Blood Stem Cell Transplantation in Patients With Hematological Malignancies
A Phase II Study to Evaluate the Efficacy of Posttransplant Cyclophosphamide for Prevention of Chronic Graft-versus-Host Disease After Allogeneic Peripheral Blood Stem Cell Transplantation
Status: Enrolling
Updated: 8/4/2015
Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium
mi
from
Seattle, WA
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Safety, Tolerability and Pharmacokinetic First in Human (FIH) Study for Intravenous (IV) TKM-100802
A Placebo-Controlled, Single-Blind, Single-Ascending Dose Study With An Additional Multiple-Dose Cohort to Evaluate the Safety, Tolerability, and Pharmacokinetics of TKM-100802 in Healthy Human Volunteers
Status: Enrolling
Updated:  8/4/2015
Healthcare Discoveries, LLC d/b/a ICON Development Solutions
mi
from
San Antonio, TX
Safety, Tolerability and Pharmacokinetic First in Human (FIH) Study for Intravenous (IV) TKM-100802
A Placebo-Controlled, Single-Blind, Single-Ascending Dose Study With An Additional Multiple-Dose Cohort to Evaluate the Safety, Tolerability, and Pharmacokinetics of TKM-100802 in Healthy Human Volunteers
Status: Enrolling
Updated: 8/4/2015
Healthcare Discoveries, LLC d/b/a ICON Development Solutions
mi
from
San Antonio, TX
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Effect of Copper Impregnated Textiles on Healthcare Associated Infections and Antibiotic Use
Effect of Copper Impregnated Textiles on Healthcare Associated Infections and Antibiotic Use in a Single Intensive Care Unit
Status: Enrolling
Updated:  8/4/2015
Sentara Norfolk General Hospital
mi
from
Norfolk, VA
Effect of Copper Impregnated Textiles on Healthcare Associated Infections and Antibiotic Use
Effect of Copper Impregnated Textiles on Healthcare Associated Infections and Antibiotic Use in a Single Intensive Care Unit
Status: Enrolling
Updated: 8/4/2015
Sentara Norfolk General Hospital
mi
from
Norfolk, VA
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Safety Surveillance of MenACWY-CRM Vaccine in Children
Post-licensure Observational Safety Surveillance Study of Quadrivalent Meningococcal ACWY Conjugate Vaccine MenACWY-CRM (Menveo) Vaccination in Children 2 Through 10 Years of Age
Status: Enrolling
Updated:  8/5/2015
Kaiser Permanente South California
mi
from
Pasadena, CA
Safety Surveillance of MenACWY-CRM Vaccine in Children
Post-licensure Observational Safety Surveillance Study of Quadrivalent Meningococcal ACWY Conjugate Vaccine MenACWY-CRM (Menveo) Vaccination in Children 2 Through 10 Years of Age
Status: Enrolling
Updated: 8/5/2015
Kaiser Permanente South California
mi
from
Pasadena, CA
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A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60
A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60 Lavage Following Abdominal Surgery as an Adjunctive Therapy to Prophylactic Systemic Antibiotics
Status: Enrolling
Updated:  8/5/2015
University of South Alabama Medical Center
mi
from
Mobile, AL
A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60
A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60 Lavage Following Abdominal Surgery as an Adjunctive Therapy to Prophylactic Systemic Antibiotics
Status: Enrolling
Updated: 8/5/2015
University of South Alabama Medical Center
mi
from
Mobile, AL
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A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60
A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60 Lavage Following Abdominal Surgery as an Adjunctive Therapy to Prophylactic Systemic Antibiotics
Status: Enrolling
Updated:  8/5/2015
University of California, San Diego, Thornton Hospital
mi
from
La Jolla, CA
A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60
A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60 Lavage Following Abdominal Surgery as an Adjunctive Therapy to Prophylactic Systemic Antibiotics
Status: Enrolling
Updated: 8/5/2015
University of California, San Diego, Thornton Hospital
mi
from
La Jolla, CA
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A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60
A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60 Lavage Following Abdominal Surgery as an Adjunctive Therapy to Prophylactic Systemic Antibiotics
Status: Enrolling
Updated:  8/5/2015
BJJS, Corp., Memorial Hermann Memorial Medical Center
mi
from
Houston, TX
A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60
A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60 Lavage Following Abdominal Surgery as an Adjunctive Therapy to Prophylactic Systemic Antibiotics
Status: Enrolling
Updated: 8/5/2015
BJJS, Corp., Memorial Hermann Memorial Medical Center
mi
from
Houston, TX
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A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60
A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60 Lavage Following Abdominal Surgery as an Adjunctive Therapy to Prophylactic Systemic Antibiotics
Status: Enrolling
Updated:  8/5/2015
University of Virginia
mi
from
Charlottesville, VA
A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60
A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60 Lavage Following Abdominal Surgery as an Adjunctive Therapy to Prophylactic Systemic Antibiotics
Status: Enrolling
Updated: 8/5/2015
University of Virginia
mi
from
Charlottesville, VA
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Comparison of Fluconazole vs Voriconazole to Treat Fungal Infections for Blood and Marrow Transplants (BMT CTN 0101)
A Randomized Double-blind Trial of Fluconazole Versus Voriconazole for the Prevention of Invasive Fungal Infections in Allogeneic Blood and Marrow Transplant Patients (BMT CTN #0101)
Status: Enrolling
Updated:  8/5/2015
University of Alabama at Birmingham
mi
from
Birmingham, AL
Comparison of Fluconazole vs Voriconazole to Treat Fungal Infections for Blood and Marrow Transplants (BMT CTN 0101)
A Randomized Double-blind Trial of Fluconazole Versus Voriconazole for the Prevention of Invasive Fungal Infections in Allogeneic Blood and Marrow Transplant Patients (BMT CTN #0101)
Status: Enrolling
Updated: 8/5/2015
University of Alabama at Birmingham
mi
from
Birmingham, AL
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Comparison of Fluconazole vs Voriconazole to Treat Fungal Infections for Blood and Marrow Transplants (BMT CTN 0101)
A Randomized Double-blind Trial of Fluconazole Versus Voriconazole for the Prevention of Invasive Fungal Infections in Allogeneic Blood and Marrow Transplant Patients (BMT CTN #0101)
Status: Enrolling
Updated:  8/5/2015
UCSD Medical Center
mi
from
La Jolla, CA
Comparison of Fluconazole vs Voriconazole to Treat Fungal Infections for Blood and Marrow Transplants (BMT CTN 0101)
A Randomized Double-blind Trial of Fluconazole Versus Voriconazole for the Prevention of Invasive Fungal Infections in Allogeneic Blood and Marrow Transplant Patients (BMT CTN #0101)
Status: Enrolling
Updated: 8/5/2015
UCSD Medical Center
mi
from
La Jolla, CA
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Comparison of Fluconazole vs Voriconazole to Treat Fungal Infections for Blood and Marrow Transplants (BMT CTN 0101)
A Randomized Double-blind Trial of Fluconazole Versus Voriconazole for the Prevention of Invasive Fungal Infections in Allogeneic Blood and Marrow Transplant Patients (BMT CTN #0101)
Status: Enrolling
Updated:  8/5/2015
Stanford Hospital and Clinics
mi
from
Stanford, CA
Comparison of Fluconazole vs Voriconazole to Treat Fungal Infections for Blood and Marrow Transplants (BMT CTN 0101)
A Randomized Double-blind Trial of Fluconazole Versus Voriconazole for the Prevention of Invasive Fungal Infections in Allogeneic Blood and Marrow Transplant Patients (BMT CTN #0101)
Status: Enrolling
Updated: 8/5/2015
Stanford Hospital and Clinics
mi
from
Stanford, CA
Click here to add this to my saved trials
Comparison of Fluconazole vs Voriconazole to Treat Fungal Infections for Blood and Marrow Transplants (BMT CTN 0101)
A Randomized Double-blind Trial of Fluconazole Versus Voriconazole for the Prevention of Invasive Fungal Infections in Allogeneic Blood and Marrow Transplant Patients (BMT CTN #0101)
Status: Enrolling
Updated:  8/5/2015
Childrens National Medical Center
mi
from
Washington,
Comparison of Fluconazole vs Voriconazole to Treat Fungal Infections for Blood and Marrow Transplants (BMT CTN 0101)
A Randomized Double-blind Trial of Fluconazole Versus Voriconazole for the Prevention of Invasive Fungal Infections in Allogeneic Blood and Marrow Transplant Patients (BMT CTN #0101)
Status: Enrolling
Updated: 8/5/2015
Childrens National Medical Center
mi
from
Washington,
Click here to add this to my saved trials