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HIV Infections clinical trials

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NCT ID: NCT00752037 Completed - HIV Infections Clinical Trials

Safety Study of Lopinavir/Ritonavir With Raltegravir in HIV-infected Patients

Start date: September 2008
Phase: Phase 4
Study type: Interventional

A single center, open label, 48-week study of lopinavir/ritonavir in combination with raltegravir. 30 patients, both naïve and experienced, will be enrolled. 15 treatment naïve patients and 15 treatment experienced patients enrolled

NCT ID: NCT00751595 Completed - HIV Infections Clinical Trials

Immunogenicity and Safety Trial of the HIV-1 Tat Vaccine

ISS T-002
Start date: September 2008
Phase: Phase 2
Study type: Interventional

The study is a randomized, open label, phase II clinical trial directed at evaluating the immunogenicity (as a primary end-point) and the safety (as a secondary end-point), of the recombinant HIV-1 Tat vaccine in HIV-1 infected adult subjects, anti-Tat antibody negative, HAART-treated with chronic suppressed HIV-1 infection, CD4+ T cell counts >= 200 cells/microliter, levels of plasma viremia < 50 copies/ml in the last 6 months prior to the screening and without a history of virologic rebound. The immunogenicity of 3 or 5 immunizations of the two different vaccine doses (7.5 and 30 micrograms) of the Tat vaccine has been evaluated.

NCT ID: NCT00751530 Completed - HIV Infections Clinical Trials

BRAVO: Background Regimen of Raltegravir on Virologic Outcome

BRAVO
Start date: March 2008
Phase: N/A
Study type: Observational

This is a retrospective chart review of participants in raltegravir expanded access program and will compare virologic response in regimens not containing a protease inhibitor in the antiretroviral background regimen to regimens containing a protease inhibitor in the background regimen.

NCT ID: NCT00751192 Completed - HIV Infections Clinical Trials

Effect of an Online Video-Based Intervention to Increase HIV Testing in Men Who Have Sex With Men in Peru

Start date: October 2007
Phase: N/A
Study type: Interventional

Men who have sex with men (MSM) account for the greatest burden of the HIV and Sexually Transmitted Infection (STI) epidemic in Peru. Current interventions that promote early identification and treatment of these diseases target a limited number of this population because they rely solely on peer education. To assess the use of the Internet as an alternative tool to reach this population the investigators propose to conduct an online randomized controlled trial to compare the effect of HIV-testing motivational videos versus standard public health text, both offered through gay websites. The methodology the investigators will use is divided in: (1) the development period, where the investigators will select gay websites for banner advertisement, create and refine effective recruitment messages and design the online survey and the video-based intervention (2) the intervention period, where participants who meet the eligibility criteria will be randomized into a video or a standard public health text. The videos will be customized for three audiences based on self-identification: gay, non-gay and trans and will be framed within the health-belief model and the stages of change theory (3) in the outcome evaluation period we will compare the 'intentions to get tested' and 'time to HIV testing at the clinic' among MSM of each of the trial arms. If the Internet is an effective venue to reach MSM for HIV testing, Peruvian health programs that target this population may start considering the delivery of web-based interventions and other online prevention services to this under served and hard-to-reach population.

NCT ID: NCT00751153 Recruiting - HIV Infections Clinical Trials

Raltegravir and Atazanavir Replacing Current Suppressive Treatment Because of Side Effects in Current Treatment

Start date: March 2008
Phase: Phase 4
Study type: Interventional

Subjects with HIV who have viral suppression on current regimen but also have side effects/intolerance will change their current regimen to a combination of Raltegravir and Atazanavir and be monitored for viral and immunological response and quality of life.

NCT ID: NCT00749840 Completed - Clinical trials for Human Immunodeficiency Virus Infections

Attitudes and Beliefs and the Steps of HIV Care

Start date: April 2008
Phase: N/A
Study type: Observational

Through a prospective observational cohort study enrolling patients newly diagnosed with Human immunodeficiency virus (HIV): Aim 1: Assess attitudes and beliefs about HIV disease and care over time and relate those attitudes and beliefs to success in following the Steps of HIV Care. Aim 2: Validate a simple visual analogue scale for assessing adherence to highly active antiretroviral therapy (HAART) in patients newly starting HAART in routine care. Aim 3: Implement latent growth curve analysis for modeling changes in attitudes and beliefs over time, and for assessing the impact of the components of the Steps of HIV Care model on health outcomes.

NCT ID: NCT00748800 Completed - HIV Infections Clinical Trials

An Affect Management Intervention for Juvenile Offenders

Start date: September 2004
Phase: Phase 1
Study type: Interventional

Adolescents are at risk for HIV because of sexual and drug behavior initiated during this developmental period. Adolescents in the juvenile justice system are at increased risk for HIV due to higher rates of substance use and psychopathology than their non-offending peers. Juvenile justice youth may therefore also be less likely to benefit from frequently used skills based interventions. It appears that emotional lability, frequently found in this population, disrupts skills learned. This project will implement and evaluate an affect management HIV prevention intervention for adolescents in a juvenile drug court program. Affect management and general health promotion interventions will be compared to determine which intervention best reduces risk behavior among adolescents in the drug court.

NCT ID: NCT00746473 Completed - HIV Infections Clinical Trials

Assessment of Cytokine Values in Serum and by RT-PCR in HIV-1 Individuals With and Without HAART

Start date: August 2004
Phase: N/A
Study type: Observational

A cross-sectional study was performed on HIV-1 infected individuals with or without antiretroviral treatment. 73 HIV-1 infected individuals were divided into three groups: G1= 15 infected individuals with or without AIDS who never received ARV; G2= 27 patients on HAART, and plasma HIV-1 RNA viral load (VL) equal or greater than 50 copies/mL and G3= 31 patients on HAART with undetectable VL for at least the past 6 months and a fourth group G4= 20 individuals chosen between blood donors without any disease sign and with negative HIV serum tests (control group). Serum cytokine levels pg/mL (ELISA) and specific mRNA expression by RT-PCR were performed on all four groups for TNF-a, IL-2, INF-g, IL-4 and IL-10. All patients were submitted to VL determination and CD4+ and CD8+T lymphocyte counts. Results analysis showed a significant comparison between groups for both methods and association between them (>80% - r2>0.80) with only one exception, in the individuals of control group, for IL-2 by ELISA determination. The cytokine profile for both methods and three patient groups was mature Th-0. The behavior of IL-2 and INF-g must be emphasized with the consequent expression on dominant Th profile. Both methods showed low IL-2 and elevated mean INF-g values in the three patient groups.

NCT ID: NCT00746369 Completed - HIV Infections Clinical Trials

IMARA, Adapting SiHLE for Detained African American Adolescent Females

IMARA
Start date: October 2008
Phase: N/A
Study type: Interventional

The IMARA Program will test the efficacy of a multi-session HIV Prevention program, adapted from an existing program(SiHLE), for incarcerated African American adolescent females.

NCT ID: NCT00745368 Completed - HIV Infections Clinical Trials

Comparing Raltegravir Genital Tract Distribution in HIV-infected Men and Women

Start date: September 2008
Phase: N/A
Study type: Interventional

The purpose of this research study is to determine how much raltegravir gets into the male and female genital tract.