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HIV Infections clinical trials

View clinical trials related to HIV Infections.

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NCT ID: NCT00272519 Completed - HIV Infections Clinical Trials

Life Skills Intervention for Adolescents Perinatally Infected With HIV

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

The life skills intervention model is designed to help adolescents promote their physical and mental health through cognitive and behavioral techniques (e.g., problem solving, coping, and communication skills) designed to help them achieve social and personal competencies used to manage various life challenges.

NCT ID: NCT00272493 Completed - HIV Infections Clinical Trials

Safety and Effectiveness of an Adjuvant in Improving Immune Response to Hepatitis B Virus Vaccine in HIV Infected Individuals

Start date: n/a
Phase: Phase 2
Study type: Interventional

Granulocyte-macrophage colony-stimulating factor (GM-CSF) is a naturally occurring substance that is made by the body in response to infection or inflammation, and greatly improves cellular immune responses. The purpose of this study is to evaluate the safety and effectiveness of GM-CSF as an adjuvant to improve the immune response to hepatitis B virus (HBV) vaccination in HIV infected individuals.

NCT ID: NCT00272220 Completed - Clinical trials for Acquired Immunodeficiency Syndrome

Longitudinal Study of HAART, Social Networks, & Adherence

Start date: October 2004
Phase: N/A
Study type: Interventional

Our study is a randomized controlled trial that aims to evaluate the effectiveness of modified directly observed therapy (mDOT) to (1) increase both short and long term adherence to HAART treatment, and (2) improve clinical outcomes associated with HAART therapy. Our hypothesis is that modified directly observed therapy (mDOT) during the initial 6 weeks of HAART, supervised primarily by HIV-positive lay activists, will improve adherence and clinical outcomes compared with those that do not have supervised mDOT. We also hypothesize that the benefits of mDOT will be achieved through a variety of mediators that will result from the social interactions the patients will have with the activists. These mediators include improved social support, improved knowledge about HAART, reduced stigma, and improved self-efficacy.

NCT ID: NCT00271960 Completed - HIV Infections Clinical Trials

Group Prenatal Care for Reducing the Risk of STDs in Pregnant Young Women

Start date: April 2001
Phase: Phase 3
Study type: Interventional

This study will determine the effectiveness of two group prenatal care programs as compared to individual prenatal care in reducing the risk for HIV, STDs and adverse perinatal outcomes in young women during and after pregnancy.

NCT ID: NCT00271908 Completed - HIV Infections Clinical Trials

C2P (With Venues): Connect to Protect® Partnerships For Youth Prevention Interventions

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

During Phase III, Adolescent Trials Network for HIV/AIDS Interventions (ATN)/Connect-to-Protect (C2P) site staff, their official community partners established in Phase I, and newly invited community sector representatives (i.e., individuals from various key parts of the community such as family, spiritual or faith-based institutions, business and government) will form a coalition that will work toward achieving C2P objectives. ATN 040b is the evaluation protocol for ATN 040, Phase III of C2P.

NCT ID: NCT00271882 Completed - HIV Infections Clinical Trials

PTSD and Risk Behavior in HIV Positive Female Adolescents

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

This is a qualitative study using a purposive sampling methodology to interview HIV-positive female adolescents who have experienced physical and/or sexual abuse. An open-ended, in-depth interview, occurring over one to two sessions, will be conducted with each participant.

NCT ID: NCT00270764 Completed - HIV Infections Clinical Trials

Social and Economic Outcomes of HIV/AIDS Care and Treatment in HIV Infected South African Adults

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

The purpose of this study is to determine the social and economic outcomes of anti-HIV treatment in South African adults, with data collected from interviews, detailed questionnaires, and patients' medical records.

NCT ID: NCT00270530 Completed - HIV Infections Clinical Trials

Intermittent Preventive Treatment of Malaria in HIV-Seropositive Pregnant Women in Zambia

Start date: November 2002
Phase: Phase 4
Study type: Interventional

Prevention of malaria in pregnancy is critical given the high incidence of malaria in Zambia and its serious impact on both maternal and infant survival. Intermittent presumptive treatment with sulfadoxine-pyrimethamine has been shown to be highly efficacious for reducing the risk of malaria in pregnancy. However, based on a study done in western Kenya, HIV-infected pregnant women may need more frequent dosing of SP, i.e., on a monthly basis rather than the standard 2-dose regimen given during the second and third trimesters, as HIV appears to reduce the effectiveness of the SP drug combination. The goal of this study was to evaluate the efficacy of the standard dosing regimen in comparison to an intensive monthly SP dosing schedule in HIV-positive women.

NCT ID: NCT00270296 Completed - HIV Infections Clinical Trials

Trizivir Vs. Kaletra and Combivir for the Prevention of Mother-to-Child Transmission of HIV

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

Anti-HIV drug regimens have dramatically improved the rates of prevention of mother-to-child transmission (MTCT) of HIV in developed countries. However, little is known of the effectiveness of such regimens in developing countries, such as Botswana. This study will determine whether Trizivir (TZV), a single pill containing abacavir sulfate, lamivudine, and zidovudine (ABC/3TC/ZDV), or lopinavir/ritonavir (LPV/r) and lamivudine/zidovudine (3TC/ZDV) is more effective in reducing HIV-1 viral load and preventing MTCT among HIV infected pregnant women in Botswana.

NCT ID: NCT00270283 Completed - Anemia Clinical Trials

A Study to Evaluate the Safety and Efficacy of Epoetin Alfa Versus Placebo for the Treatment of Anemia in Patients With Acquired Immunodeficiency Syndrome (AIDS) Who Are Receiving Zidovudine (AZT) Therapy

Start date: July 1988
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effectiveness and safety of epoetin alfa in AIDS patients for the treatment of anemia that is a result of the disease and zidovudine (AZT) treatment. Epoetin alfa is a genetically engineered protein that stimulates red blood cell production.