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HIV-1 Infection clinical trials

View clinical trials related to HIV-1 Infection.

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NCT ID: NCT04067869 Completed - HIV-1-infection Clinical Trials

Cytomegalovirus Infection in Patients With HIV-1 Infection

ACTHIV
Start date: February 16, 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the level of CD4 and CD8 T cell activation in an observational cohort study of HIV-1 patients, virosuppressed on combined antiretroviral therapy (< 50 copies/ml) for at least 2 years and to focus on two factors that could participate in this activation: cytomegalovirus infection and auto-immune disorders.

NCT ID: NCT04067219 Completed - HIV-1-infection Clinical Trials

SkIn, Muscle and Bone Aging Determinants in HIV Infected-patients.

SIMBAD
Start date: May 3, 2012
Phase: N/A
Study type: Interventional

this study consists of the study of markers of skin, muscular, neurocognitive and bone aging in HIV infected adults and to compare the frequency of these signs to the general population of same gender and age.

NCT ID: NCT04066036 Completed - HIV-1-infection Clinical Trials

Population Effectiveness of Dolutegravir Implementation in Sub-Saharan Africa

DISCO
Start date: May 14, 2019
Phase:
Study type: Observational

This is a prospective observational cohort study enrolling participants in South Africa and Uganda who are prescribed an HIV treatment regimen containing lamivudine, tenofovir, and dolutegravir, which is known as TLD. We hope to better understand how effective TLD will be in sub-Saharan Africa. If treatment failure occurs, we seek to understand the possible reasons, including drug resistance and adherence challenges.

NCT ID: NCT04063306 Recruiting - HIV-1-infection Clinical Trials

Quality of Life of Taiwan People Living With HIV

Start date: June 20, 2019
Phase:
Study type: Observational [Patient Registry]

To survey QoL and relevant factors in PLWH

NCT ID: NCT04061889 Recruiting - HIV-1 Infection Clinical Trials

Clinical Epidemiology Cohort Study for Patient Living With HIV

Start date: April 1, 2019
Phase:
Study type: Observational

This is a retrospective observational cohort study for the patient living with HIV aiming to understand more in disease progress, resistant mutation, comorbidity, and common coinfection.

NCT ID: NCT04051970 Active, not recruiting - HIV-1-infection Clinical Trials

Reducing Antiretroviral Treatments

ALTAR
Start date: November 27, 2019
Phase: Phase 3
Study type: Interventional

The purpose of this trial is to demonstrate at W48 the non-inferiority of a dual nucleoside analogues strategy with tenofovir (TDF) or tenofovir alafenamide (TAF) plus emtricitabine (FTC) or lamivudine (3TC) preceded by a 16 week induction period with TDF or TAF plus FTC or 3TC plus an integrase inhibitor (INI) relative to an immediate 2-DR strategy with dolutegravir plus 3TC in HIV-infected antiretroviral therapy (ARV) naïve participants with CD4 cells count greater than 300/mm3 and a low viral load defined as plasma HIV RNA strictly lower than 50 000 cp/mL

NCT ID: NCT04050735 Recruiting - Alcohol Drinking Clinical Trials

Acute Neural and Immune Effects of Alcohol in People Living With HIV Infection

Start date: May 19, 2021
Phase: N/A
Study type: Interventional

This study will examine whether moderate alcohol use in the context of HIV infection exacerbates inflammatory signaling in the immune system and brain. The study will recruit healthy individuals and people living with HIV infection who are otherwise in good health to participate. Participants will complete an experimental protocol that involves controlled alcohol administration and magnetic resonance imaging (MRI). Primary outcomes are plasma biomarkers of inflammation and MRI markers correlated with neuroinflammation. Results will advance understanding of the effects of alcohol use in people living with HIV infection.

NCT ID: NCT04050449 Completed - HIV-1-infection Clinical Trials

Assess Therapeutic Efficacy and Emergence of HIV Drug Resistance Following Initiation of TLD

Start date: October 28, 2019
Phase:
Study type: Observational

Tenofovir disoproxil fumarate/lamivudine/dolutegravir (TLD) is being used more widely across the world to treat HIV. This is an observational study (a type of study in which participants are observed and certain outcomes are measured). The aim of this study is to observe how successful TLD is at treating HIV, in the following groups of people: - People switching to TLD, after taking anti-HIV medication that contains a nonnucleoside reverse transcriptase inhibitor (NNRTI) drug (such as Efavirenz or Nevirapine) (Group 1). - People switching to TLD, after taking anti-HIV medication that contains a boosted protease inhibitor (PI) drug (such as Lopinavir or Atazanavir) (Group 2). - People taking TLD and receiving medication for TB that includes the drug rifampicin (RIF) (Group 3). These people must be starting one or both of these medications when they enter the study. - People starting TLD who have not taken anti-HIV medication before (Group 4). Another goal of this study is to use genetic testing of the virus (HIV) to see how often HIV is resistant to TLD. Genetic testing of the virus is one way to see if the TLD medication is not working to treat a person's HIV infection.

NCT ID: NCT04041362 Withdrawn - HIV-1 Infection Clinical Trials

the Study to Evaluate the Safety of UB-421 in Combination With Antiretroviral Therapy (ART) and the Efficacy in Reduction of HIV Viral Load and Proviral DNA as Compared to ART Alone in ART-experienced Viremic HIV-1 Patients

Start date: April 2020
Phase: Phase 2
Study type: Interventional

This study assess the safety, tolerability, and efficacy in reducing viral load and proviral DNA of UB-421 administered as an add-on to the ART in ART-experienced viremic HIV-1 subjects.

NCT ID: NCT04040075 Terminated - HIV-1-infection Clinical Trials

Testing the Safety and Efficacy of Commercial Drug Biktarvy in Subjects Known to Have the 184 Resistance Mutation to a Component in Biktarvy

Start date: July 1, 2019
Phase: Phase 4
Study type: Interventional

An Open-Label Study to Evaluate Switching from a Regimen of Elvitegravir/Tenofovir alafenamide/Emtricitabine/Cobicistat and Darunavir, to a Fixed-Dose Combination of Bictegravir/Tenofovir alafenamide/Emtricitabine in Virologically Suppressed HIV-1 Subjects who are known to have a I84 V/I Mutation