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NCT ID: NCT01145677 Completed - Alcohol Dependence Clinical Trials

Efficacy of Topiramate for Hospitalized Patients With Alcoholism

ETHoPA-R
Start date: June 2010
Phase: Phase 2/Phase 3
Study type: Interventional

This is a 12-Week, randomized controlled study of topiramate in hospitalized patients with alcoholism

NCT ID: NCT01144338 Completed - Clinical trials for Type 2 Diabetes Mellitus

Exenatide Study of Cardiovascular Event Lowering Trial (EXSCEL): A Trial To Evaluate Cardiovascular Outcomes After Treatment With Exenatide Once Weekly In Patients With Type 2 Diabetes Mellitus

Start date: June 18, 2010
Phase: Phase 3
Study type: Interventional

This study will compare the impact of including exenatide once weekly in addition to usual care vs. usual care without exenatide on major cardiovascular outcomes as measured by the primary composite endpoint of cardiovascular-related death, nonfatal myocardial infarction (MI), or nonfatal stroke.

NCT ID: NCT01143064 Completed - Brain Injuries Clinical Trials

Efficacy and Safety Study of Intravenous Progesterone in Patients With Severe Traumatic Brain Injury

SyNAPSe
Start date: June 2010
Phase: Phase 3
Study type: Interventional

The SyNAPSe trial will study if giving intravenous (i.v.) progesterone within 8 hours of the injury for a total of 120 hours to severe traumatic brain injury patients improves their recovery.

NCT ID: NCT01140347 Completed - Clinical trials for Hepatocellular Carcinoma

A Study of Ramucirumab (IMC-1121B) Drug Product (DP) and Best Supportive Care (BSC) Versus Placebo and BSC as 2nd-Line Treatment in Participants With Hepatocellular Carcinoma After 1st-Line Therapy With Sorafenib

REACH
Start date: October 2010
Phase: Phase 3
Study type: Interventional

This is a Phase 3 multicenter, randomized study evaluating the safety and efficacy of ramucirumab DP plus BSC as a double-blind, placebo-controlled (placebo plus BSC) comparison. Approximately 544 participants, at least 18 years of age, with Child-Pugh score < 7 and diagnosed with hepatocellular carcinoma will be randomized. Participants must have received sorafenib as first-line systemic treatment for hepatocellular carcinoma (HCC), and must have discontinued sorafenib prior to entering the study. Hypothesis: This sample size will allow differentiation of the expected increase in median overall survival (OS), from 8 months in the placebo arm to 10.67 months in the ramucirumab arm. Upon registration and completion of screening procedures, eligible participants with HCC who have disease progression during or following first-line therapy with sorafenib, or were intolerant to this agent, will be randomized to receive either ramucirumab DP or placebo. The treatment regimen will be continued until radiographic or symptomatic progression, the development of unacceptable toxicity, noncompliance or withdrawal of consent by the participant, or investigator decision.

NCT ID: NCT01139905 Completed - HIV-1 Infections Clinical Trials

Lopinavir/Ritonavir (LPV/r) Tablet in HIV Infected Children

Start date: April 2010
Phase: Phase 2
Study type: Interventional

To study the pharmacokinetics of low-dose lopinavir/ritonavir tablet in HIV-1 infected Thai children.

NCT ID: NCT01138267 Completed - HIV Infections Clinical Trials

Pharmacogenomic of Atazanavir/Efavirenz (ATV/EFV)

Start date: May 2009
Phase:
Study type: Observational

Objectives: - To evaluate the impact of genetic polymorphism on ARV drug levels - To evaluate the effect of genetic polymorphism/drug levels on long term immunologic and virologic response - To correlate the genetic polymorphism/drug levels on antiretroviral toxicities The long-term objective of this research plan is to characterize impact of pharmacogenomics to HIV drug concentration, toxicities, and response to antiretroviral therapy among HIV-infected adults. A comprehensive understanding of the impact of pharmacogenomics to HIV infection and HIV medication will lead to the development of appropriate intervention such as dose reduction strategies in patients with particular gene(s) correlated with higher drug levels. The dose reduction strategy will decrease long term drug toxicity and cost saving for Thais and Asian Ethnicities.

NCT ID: NCT01138241 Completed - HIV Infection Clinical Trials

Tenofovir Renal Toxicity and Glomerular Filtration Rate (GFR) Validation

Start date: March 2010
Phase:
Study type: Observational

To assess and validate equation eGFR in HIV-infected subjects and -uninfected Thai patients

NCT ID: NCT01138215 Completed - HIV Infections Clinical Trials

The Immunogenicity of Varicella-zoster Virus Vaccine in HIV-infected Children

Start date: June 2009
Phase: Phase 4
Study type: Interventional

To study about the immunogenicity, safety and efficacy of varicella-zoster virus vaccine in HIV-infected children.

NCT ID: NCT01138202 Completed - HIV Infections Clinical Trials

Pharmacokinetics (PK) and Safety of 2 Different Doses of Lopinavir/Ritonavir in in HIV/Tuberculosis (TB) Co-infected Patients Receiving Rifampicin Containing Anti-tuberculosis Therapy

Start date: November 2010
Phase: Phase 2
Study type: Interventional

To assess safety, efficacy and impact of Lopinavir/ritonavir 400/100mg bid or Lopinavir/ritonavir 600/150mg bid in combination with rifampicin-containing anti-TB therapy.

NCT ID: NCT01137045 Completed - Rabies Clinical Trials

Immunogenicity and Safety Study of A New Chromatographically Purified Vero Cell Rabies Vaccine With ID Regimen and ERIG

Start date: June 2010
Phase: Phase 4
Study type: Interventional

A comparative,randomized (1:1)study to evaluate the safety and immunogenicity of a new chromatographically purified vero cell rabies vaccine (SPEEDA) and chromatographically purified vero cell rabies vaccine (SPEEDA)which is filled by Queen Saovabha Memorial Institute (TRCS SPEEDA)vs. reference vaccine (purified vero cell vaccine; VERORAB)when using with post-exposure rabies intradermal vaccination with or without equine rabies immunoglobulin.