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HIV Infections clinical trials

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NCT ID: NCT01043081 Completed - HIV Infections Clinical Trials

Sexually Transmitted Infections Among African American Women Who Have Sex With Women

WSW
Start date: February 2009
Phase: N/A
Study type: Observational

The purpose of this study is to determine the rates of sexually transmitted infections (STI) among a group of African American women who have sex with women (AA WSW). The first study hypothesis is that AA WSW are at risk for acquiring and transmitting STI, including the human immunodeficiency virus (HIV). The second study hypothesis is that AA WSW participate in multiple high-risk sexual activities that may facilitate transmission of STIs, including HIV.

NCT ID: NCT01042808 Completed - HIV Infections Clinical Trials

Isentress Re-examination Study (MK-0518-115)

Start date: May 2011
Phase: N/A
Study type: Observational

This survey is conducted for preparing application materials for re-examination under the Pharmaceutical Affairs Laws and its Enforcement Regulation, its aim is to reconfirm the clinical usefulness of Isentress through collecting the safety and efficacy information in usual practice according to the Re-examination Regulation for New Drugs. Post-marketing surveys are not considered applicable clinical trials and thus the results of this survey will not be posted at its conclusion. The results will be submitted to public health officials as required by applicable national and international laws.

NCT ID: NCT01041521 Completed - HIV Infection Clinical Trials

The Impact of Omega Three Fatty Acids on Vascular Function in HIV

HOST
Start date: January 2010
Phase: Phase 4
Study type: Interventional

The study seeks to determine if the use of omega three fatty acids in individuals infected with HIV and with high triglycerides leads to improved triglyceride levels, better blood vessel function and decrease in the amount of obstruction in blood vessels.

NCT ID: NCT01040091 Completed - HIV Infections Clinical Trials

Evaluation of the Cellular Pharmacology of Tenofovir and Emtricitabine According to HIV Infection Status

Start date: December 2009
Phase: Phase 1
Study type: Interventional

Tenofovir disoproxil fumarate (TDF) and emtricitabine (FTC) are two antiretroviral medications used for the treatment and prevention of HIV/AIDS. This study will examine how these medications are processed in the body of people who are HIV-infected, as well as in people who are HIV-uninfected.

NCT ID: NCT01039220 Completed - HIV Infections Clinical Trials

Incidence of H1N1v Influenza-like Illness and Risk Factors for Serious Influenza Forms in HIV Infected Patients

ANRS 2H
Start date: December 2009
Phase: N/A
Study type: Interventional

To estimate the incidence of H1N1v influenza-like illness and to study the risk factors for serious influenza forms during pandemic period in French HIV infected patients. - Definitions: - Influenza like illness is defined as fever> 37°8C and cough or pharyngalgia. (Centers for Disease Control definition). - Serious forms of influenza-like illness is defined by hospitalization within 14 days onset of symptoms or death attributed to influenza like illness. - Design: - Survey sampling for estimating H1N1v influenza-like illness incidence. - Out of approximately 50 000 patients under follow-up in one of the 40 ANRS centres, a sub-group will be selected by random sampling. Sampling will be stratified by centre and sampling fraction per site will vary in order to select 60 to 80 patients for this study per site. A total of 2500 to 3000 patients will be selected to allow for estimating the incidence of H1N1v influenza-like illness with an adequate precision. Selected patients will be asked to contact the clinical staff on site as soon as any influenza like symptoms appear. In the case of influenza like illness patients are requested to attend to the clinic within 24 hours for physical examination and naso-pharyngeal swab for diagnosis of A(H1N1)v infection. Nested case-control study for the determination of risk factors for serious forms: - Cases: Serious forms (see definition above) identified by any clinical site or hospitalisation unit. - Controls: Patients of the randomly selected sample (see survey sampling above), presenting with influenza-like illness without any criterion for severity. Exhaustivity check: The exhaustivity of symptomatic forms will be assessed a posteriori by merging information from all available data sources.

NCT ID: NCT01038999 Completed - HIV Infection Clinical Trials

Accelerated Aging, HIV Infection, Antiretroviral Therapies

EP 45
Start date: April 2009
Phase: N/A
Study type: Observational

The main goal is to confirm, among HIV1-infected patients, data from in vitro studies showing that antiretroviral therapies induce an accelerated aging through the same mechanisms than genetic laminopathies or than "physiological " aging, that is through the synthesis and persistence of farnesylated prelamin A. The secondary goal is to measure the impact of HIV infection and of antiretroviral therapies on markers of cell ageing (proteasome, mitochondria, telomere). The perspective is to fix antiretroviral therapy side effects using the same drug combination that will be used in few weeks in Marseille to treat children suffering from progeria

NCT ID: NCT01038401 Completed - HIV Infection Clinical Trials

Residual Replication of HIV-1 in the Gut Associated Lymphoid Tissue (GALT) of Patients on Highly Active Antiretroviral Therapy (HAART): the ANRS EP 44 Study

EP 44
Start date: September 2008
Phase: N/A
Study type: Interventional

HIV-1 cannot be eradicated from infected individuals by current antiretroviral regimens. Cellular reservoirs and tissue sanctuary sites allow latent HIV-1 persistence and ongoing low-level virus replication. This project aims to characterize the residual replication of HIV-1 in subjects on antiretroviral therapy, particularly in the gut-associated lymphoid tissue.

NCT ID: NCT01038076 Completed - HIV Infections Clinical Trials

Medications for Chronic HIV: Education and Collaboration

MedCHEC
Start date: December 2009
Phase: N/A
Study type: Interventional

This study will examine whether a computerized, self-administered assessment of patient medication adherence and health behaviors, plus support for adherence, improves the ability of clinicians to identify adherence problems and leads to better adherence.

NCT ID: NCT01034800 Completed - HIV Infections Clinical Trials

The Neuropsychiatric Evaluation of HIV-Positive and Negative Drug Using Individuals: Study 215

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

The lack of success in treating substance abuse may be contributed to by a limited understanding of the clinical neurobiology of drug abuse. A better understanding of such deficits might aid in the development of more relevant pharmacological and psychosocial treatment approaches. Thus, the purpose of this study is to test the hypothesis that repetitive illicit drug use may be associated with cortical and subcortical structural abnormalities, vascular abnormalities, as well as neuropsychological decrements. Additionally, a battery of psychological tests are administered to provide information about demographics, drug use, neurocognitive measures, and personality structures....

NCT ID: NCT01033760 Completed - HIV-1 Infections Clinical Trials

Optimisation of Primary HIV1 Infection Treatment(ANRS 147 OPTIPRIM)

Start date: April 2010
Phase: Phase 3
Study type: Interventional

The purpose of this trial is to assess the impact of raltegravir, maraviroc, darunavir/r, and Truvada® (emtricitabine/tenofovir) vs. darunavir/r and Truvada® on cell-associated HIV-DNA levels in patients with primary HIV-1 infection.