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HIV Seropositivity clinical trials

View clinical trials related to HIV Seropositivity.

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NCT ID: NCT02011958 Completed - Clinical trials for Visceral Leishmaniasis

Efficacy Trial of Ambisome Given Alone and Ambisome Given in Combination With Miltefosine for the Treatment of VL HIV Positive Ethiopian Patients.

Start date: July 2014
Phase: Phase 3
Study type: Interventional

The overall objective of this trial is to identify a safe and effective treatment for visceral leishmaniasis (VL) in HIV co-infected Ethiopian patients. Patients will receive either Ambisome alone or Ambisome in combination with Miltefosine. Patients who do not undergo treatment failure will be given a VL prophylactic treatment with Pentamidine one month after the end of the study treatment.

NCT ID: NCT02003989 Completed - HIV Seropositivity Clinical Trials

Revealing Increased Axonal Loss in Treated HIV Patients

OCTIHIV
Start date: May 2013
Phase: N/A
Study type: Observational

HIV patients may suffer sooner from aging than average population, including brain aging. Our hypothesis is that if brain dysfunctions are explained by a quicker loss of neurons in HIV patients, this loss could be detected earlier by a thinning down of retinal nerve fiber layer (RNFL), compared to non HIV patients of the same age.

NCT ID: NCT01957917 Completed - HIV Clinical Trials

Comparing Food and Cash Assistance for HIV-Positive Men and Women on Antiretroviral Therapy in Tanzania

Start date: December 2013
Phase: N/A
Study type: Interventional

The importance of good nutrition and food security among people living with HIV infection (PLHIV) is widely recognized. In resource-constrained settings, food insecurity is increasingly recognized as an important barrier to retention in care and adherence to antiretroviral therapy (ART). However, there are few studies demonstrating that food and nutrition assistance programs can improve HIV-related outcomes. This study will address this gap by comparing the effectiveness of three models for short-term support for PLHIV. Food insecure women and men on ART will be randomized into one of three groups: 1) nutrition assessment and counseling (NAC) alone, 2) NAC plus food assistance, or 3) NAC plus cash transfers. The investigators will compare the effect of the three approaches on ART adherence and retention in care after 6, 12, and 24-36 months of follow-up. The investigators hypothesize that NAC plus short-term support in the form of food or cash assistance will result in better adherence to ART and retention in care than NAC alone, and that the effects of NAC plus food assistance will be the same as NAC plus cash assistance. The results from the study will provide evidence about which assistance modalities for PLHIV work best to improve ART adherence and retention in care, and under what conditions. This study will be conducted in Shinyanga Region, Tanzania, where approximately 17 percent of households have poor or borderline food consumption and 7.4 percent of people are living with HIV infection.

NCT ID: NCT01957748 Completed - HIV Positive Clinical Trials

CCTG 594: Engagement and Retention in Care for HIV+

Start date: October 8, 2013
Phase: N/A
Study type: Interventional

CCTG 594 is a controlled, unblinded, two-arm, randomized (1:1) clinical trial to evaluate the effectiveness of a clinic-based HIV ALERT specialist on improving endpoints of retention in care and maintenance of ART as compared to the current standard of care (SoC) in HIV primary care clinics.

NCT ID: NCT01941121 Completed - HIV Positive Clinical Trials

CCTG 593: Testing and Linkage to Care

Start date: July 26, 2013
Phase: N/A
Study type: Interventional

This is a CCTG sponsored project to determine if those recently screened for HIV would accept assistance to be linked into appropriate health services. After receiving their HIV results, high-risk individuals who test negative will have an option to be linked into a study that offers them Pre-exposure Prophylaxis (PrEP), and individuals who test positive will have an option to be linked into care. If they accept, tested individuals will be in contact with an ALERT specialist that will help facilitate their linkage. The study's primary analysis will analyze how many HIV screened individuals accept the ALERT specialist assistance.

NCT ID: NCT01910493 Completed - HIV-positive Clinical Trials

Evaluation of the Impact of Mobile Phone Messages on ART and PMTCT Adherence in Mozambique

SMSaude
Start date: November 2011
Phase: N/A
Study type: Interventional

Mobile phone SMS are increasingly used to promote positive health behaviour with an aim to improve health outcomes. However, robust data on the efficacy of SMS on health seeking behaviour and patient outcomes in resource-limited settings is sparse. The SMSaude study aims to assess whether regular SMS-reminders improve retention on antiretroviral therapy (ART) and prevention of mother to child transmission of HIV (PMTCT) programmes in Mozambique.

NCT ID: NCT01898754 Completed - HIV Positive Clinical Trials

Oligonucleotide Ligation Assay (OLA) Resistance Study

OLA
Start date: May 2013
Phase: N/A
Study type: Interventional

The investigators propose to gauge improvements in the rate of durable suppression of viral replication by ART when OLA is used to guide clinical decisions at the PEPFAR Coptic Hope Center in Kenya, and to determine the cost-effectiveness of implementing this strategy at Coptic Hope Center.

NCT ID: NCT01881971 Completed - HIV Seropositivity Clinical Trials

Statins for Pulmonary and Cardiac Complications of Chronic HIV - Coordinating Center

SPARC
Start date: May 2013
Phase: Early Phase 1
Study type: Interventional

Hypothesis: Statin therapy will decrease inflammation and slow progression of cardiopulmonary abnormalities in HIV.

NCT ID: NCT01824628 Completed - Clinical trials for QT and Corrected QT Intervals Prolongation in HIV Positive Subjects Treated With an Antiretroviral Regimen

Comparison of the QT/QTc Interval Between an Outpatient HIV-Infected Population on Antiretroviral Therapy and Two Large HIV-Negative Cohorts

QTVIE
Start date: March 2013
Phase: N/A
Study type: Observational

This is a unicentric, two cohorts, observational transversal study. The purpose of this study is to compare the QT/QTc intervals of HIV positive subjects receiving an antiretroviral therapy and those without HIV in an ambulatory care setting.

NCT ID: NCT01818258 Completed - HIV Positive Clinical Trials

IMPAACT P1092: Steady State PK in Malnourished HIV Infected Children

Start date: October 26, 2015
Phase: Phase 4
Study type: Interventional

Children living with HIV from sub-Saharan Africa often present with severe malnutrition. In severe malnutrition, metabolic and/or gut structural derangement may lead to inadequate antiretroviral (ARV) absorption and/or erratic drug levels. The greater surface area to weight ratio in severely malnourished children could also place them at higher risk of under dosing compared to children with mild to moderate malnutrition. However, limited data are available on the pharmacokinetics of ARVs in severely malnourished children. This study addressed this critical gap in knowledge by evaluating the PK of zidovudine (ZDV), lamivudine (3TC), and lopinavir/ritonavir (LPV/r) in severely malnourished children living with HIV, compared to children with normal nutrition to mild malnutrition living with HIV.