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HIV Infections clinical trials

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NCT ID: NCT00351442 Completed - HIV Infections Clinical Trials

Examining Factors That May Influence Resistance to HIV-1 Infection

Start date: February 2007
Phase: N/A
Study type: Observational

Some people who are exposed to the HIV-1 virus are capable of either controlling or completely preventing viral infection. Multiple genetic factors may contribute to preventing or controlling HIV-1 infection. The purpose of this study is to analyze the immune system responses of individuals who are exposed to HIV-1 but remain uninfected.

NCT ID: NCT00350623 Terminated - HIV Infections Clinical Trials

Investigation of V520 in a HIV Vaccine Dose Refinement Study (V520-027)(TERMINATED)

Start date: October 2006
Phase: Phase 2
Study type: Interventional

This study will test the safety and immunogenicity of an investigational Human Immunodeficiency Virus (HIV) vaccine. Immunogenicity will be measured by evaluating the immune response to several different dose levels.

NCT ID: NCT00350272 Completed - HIV Infections Clinical Trials

Elvucitabine/Efavirenz/Tenofovir Versus Lamivudine/Efavirenz/Tenofovir in Human Immunodeficiency Virus (HIV)-1 Infected, Treatment-naive Participants

Start date: May 2006
Phase: Phase 2
Study type: Interventional

Elvucitabine, a novel nucleoside analog, is being studied as a treatment for participants with human immunodeficiency virus (HIV)-1. This Phase 2 study will enroll 60 HIV-1-naive participants to assess the efficacy and safety of elvucitabine compared to lamivudine in combination with tenofovir and efavirenz as measured by changes in the participant's HIV-ribonucleic acid (RNA) level and CD4 cell count. The study treatment will be 12 weeks of blinded study medication followed by an additional 84 weeks of open-label treatment if the participant's response to treatment meets certain endpoints. The pharmacokinetics of elvucitabine will also be assessed during the study.

NCT ID: NCT00348868 Completed - HIV Infection Clinical Trials

Buprenorphine HIV Care Integration Project

Start date: July 2006
Phase: N/A
Study type: Interventional

A007 is a randomized, two-arm study evaluating the effectiveness of standard drug addiction counseling with buprenorphine/naloxone to enhanced motivational drug counseling with buprenorphine/naloxone for the treatment for opioid addiction in an integrated and nonintegrated HIV care setting.

NCT ID: NCT00346762 Completed - HIV Infections Clinical Trials

Evaluating Host and Viral Factors Among HIV Infected Former Commercial Blood Donors in Fuyang, Anhui Province, China

Start date: September 2005
Phase: N/A
Study type: Observational

HIV infected former commercial blood donors (FBDs) in Fuyang, Anhui Province, China were infected with HIV from a common-source exposure to contaminated blood. The purpose of this study is to examine the role of host and viral factors in HIV disease progression in this unique HIV infected population.

NCT ID: NCT00346697 Completed - HIV Infections Clinical Trials

Omega-3 Fatty Acids for High Triglycerides in HIV-infected Patients

Start date: October 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of omega-3-fatty acids in HIV-infected patients with hypertriglyceridemia. In addition, we, the researchers, will evaluate the effect of omega-3 fatty acid administration of markers of bone turnover and inflammation.

NCT ID: NCT00346567 Completed - HIV Infections Clinical Trials

Backup With Combivir or Single Dose (SD) Truvada in Order to Avoid Non-nucleoside Reverse Transcriptase Inhibitor (NNRTI) Resistance After SD Nevirapine for the Prevention of Mother-to-child Transmission (PMTCT)

Start date: June 2006
Phase: N/A
Study type: Interventional

The aim of the study is to find short course alternatives to single dose (sd)nevirapine for the prevention of mother-to-child HIV-transmission with the same or better degree of transmission protection than sd nevirapine but with less NNRTI resistance development.

NCT ID: NCT00346476 Completed - HIV Infections Clinical Trials

Characteristics and Prevalence of Tuberculosis and HIV in Masiphumelele Township, Cape Town, South Africa

Start date: April 2006
Phase: N/A
Study type: Observational

The purpose of this study is to determine the number of people infected with tuberculosis (TB) in the Masiphumelele Township of Cape Town, South Africa, a community with high rates of TB and HIV. This study will also examine the genetics of TB and the relationships among active TB infection, new HIV infections, and HIV disease progression.

NCT ID: NCT00344981 Completed - HIV Infections Clinical Trials

Safety and Durability ofTenofovir and a Cell Cycle Agent for Viral Suppression

HADIT
Start date: June 2003
Phase: N/A
Study type: Interventional

Study Hypothesis Evaluation of the durability of the combination Tenofovir and Hydroxyurea to maintain viral suppression below 50 copies/ml in volunteers who have achieved viral suppression on a standard HAART regimen.

NCT ID: NCT00344760 Completed - HIV Infections Clinical Trials

A Study to Evaluate of the Efficacy of Enfuvirtide During the Induction Phase of Therapy

Start date: January 2005
Phase: Phase 4
Study type: Interventional

We hypothesize that using a potent antiretroviral such as Enfuvirtide during the induction phase of HAART therapy will lead to faster clearance of virus and infected cells, and lower number of minority variant HIV-1 strains.