Clinical Trials Logo

HIV Prevention clinical trials

View clinical trials related to HIV Prevention.

Filter by:

NCT ID: NCT03387462 Completed - HIV Prevention Clinical Trials

DOT Diary Optimization Pilot: A Pilot Study to Optimize the DOT Diary App to Measure PrEP Adherence

Start date: February 28, 2018
Phase: Phase 4
Study type: Interventional

The researchers are working with a technology company, AiCure, to develop a smartphone app, DOT Diary, which combines two drug adherence strategies. DOT Diary reminds people when it is time to take their medication, and uses motion-sensing technology to visually and automatically confirm the pill was swallowed. The goal of this study is to understand people's experiences using this new app while taking HIV pre-exposure prophylaxis (PrEP) for the prevention of HIV.

NCT ID: NCT03327155 Completed - HIV Prevention Clinical Trials

Western Australian Pre-exposure Prophylaxis for HIV Implementation Trial

PrEPIT-WA
Start date: November 16, 2017
Phase: Phase 3
Study type: Interventional

Despite all prevention efforts, many people in Australia continue to be infected with HIV. The Seventh National HIV Strategy 2014-2017 in Australia aims to work towards the elimination of HIV transmission by the year 2020. This project will evaluate a new additional way to lower people's chances of getting HIV. It will provide pre-exposure prophylaxis (PrEP) to people who are at high risk for HIV and evaluate what impact this new prevention approach will have on HIV in WA at the community level. The drug used in PREPIT-WA is called generic TDF/FTC (made by Mylan Laboratories Ltd.). The generic TDF/FTC is a single tablet made up of two HIV medications: tenofovir disoproxil fumarate and emtricitabine (a combination known as TDF/FTC). TDF and FTC have been widely used for many years to treat HIV. When used with other medicines in people who already have HIV, TDF/FTC reduces the amount of HIV virus in the blood. TDF/FTC does not cure HIV or AIDS, and it is not an HIV vaccine. As a treatment for people who already have HIV, TDF/FTC is approved for use in most of the world, including Australia. As a medicine for PrEP, to lower chances of HIV in those who are not infected, TDF/FTC has been approved in the US, and Truvada® (which contains TDF/FTC made by Gilead Sciences Inc.) was approved for PrEP in Australia in May 2016. At the start of the project, the generic TDF/FTC is not approved in Australia for the use as PrEP but it may become registered for use and more freely available in Australia in the future.

NCT ID: NCT03313310 Completed - HIV Prevention Clinical Trials

ATN 151 Work-to-Prevent: Employment as HIV Prevention

W2P
Start date: March 20, 2018
Phase: N/A
Study type: Interventional

The investigators aim to pilot-test a novel social and structural-level HIV intervention for YMSM and YTW of color ages 16-24.

NCT ID: NCT03270969 Completed - HIV Prevention Clinical Trials

A Pharmacokinetic Evaluation of Tenofovir/Emtricitabine as HIV Pre-Exposure Prophylaxis in Transgender Women

Start date: January 5, 2018
Phase: Phase 1
Study type: Interventional

Human immunodeficiency virus (HIV) persists worldwide as an immense health burden among vulnerable populations. HIV pre-exposure prophylaxis (PrEP) has offered the promise of limiting the global burden of HIV. The objective of this proposal is to conduct a pharmacokinetic (PK) study in transgender women to describe the pharmacokinetics of tenofovir disoproxil fumarate/emtricitabine (TDF/FTC) as PrEP within this population.

NCT ID: NCT03213366 Completed - HIV Prevention Clinical Trials

Social Media Based Peer-Led Intervention for HIV Prevention

Start date: June 16, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to test the feasibility, acceptability, and preliminary efficacy of E-PrEP on reaching young men of color who have sex with men (YMCSM) at high-risk of HIV infection to reduce HIV acquisition. E-PrEP is a peer-designed social media-based health intervention to increase PrEP awareness, knowledge, and motivation as a tool for HIV prevention and to increase linkage to primary care.

NCT ID: NCT03194308 Completed - HIV Prevention Clinical Trials

Safer Conception for Women - Understanding Use of Periconception PrEP

Start date: November 13, 2017
Phase: Phase 4
Study type: Interventional

Women who choose to conceive with an infected or unknown serostatus partner in HIV-endemic settings need prevention strategies to reduce periconception HIV acquisition risk. Women at high risk for acquiring HIV during pregnancy need risk reduction strategies to protect themselves and their babies. Evaluating uptake of and adherence to antiretrovirals as pre-exposure prophylaxis in this population is crucial to understanding whether and how this novel prevention strategy should be incorporated into HIV-risk reduction packages for at- risk women planning or with pregnancy.

NCT ID: NCT03148171 Completed - HIV Prevention Clinical Trials

Project WERK (Wellness Encouragement Respect Kinship)

WERK
Start date: October 9, 2017
Phase: N/A
Study type: Interventional

The Project WERK intervention is a brief, theory based and culturally sensitive intervention designed to capitalize on organic yet underutilized social support networks in the lives of young black men who have sex with men (YBMSM). The intervention has been developed with input from clients and their support network members, case managers, social workers, primary care providers. The goal of the intervention is to improve retention in PrEP care for young Black MSM.

NCT ID: NCT03138135 Completed - Clinical trials for Sexually Transmitted Diseases

HOME Study: a Combination Support Package to Increase Uptake of PrEP and HIV/STI Testing

Start date: January 9, 2017
Phase: N/A
Study type: Interventional

Home HIV self-testing has been FDA approved and allows users to read their own HIV test results at home, while home sexually transmitted infection (STI) test self-collection allows men to use a swab at home and mail it in for testing. The purpose of this study is to learn how Men who have Sex with Men (MSM) use these new testing options, a set of online support tools, and the option to test with someone to support them (a testing "buddy"). We will also evaluate whether the online tools help these men to connect with HIV prevention services such as Pre-Exposure Prophylaxis (PrEP) if they test HIV negative, and to HIV care services if they test HIV positive.

NCT ID: NCT03132285 Completed - HIV Prevention Clinical Trials

Safety and Acceptability Study of PrePex Device When Removing the Foreskin Shortly After Placement of Device

Start date: March 11, 2017
Phase: N/A
Study type: Interventional

To assess the safety and acceptability of the non-surgical PrePex device among healthy adult male participants scheduled for voluntary medical male circumcision when removing the foreskin shortly after device placement.

NCT ID: NCT03082690 Completed - HIV Prevention Clinical Trials

ImQuest (IQP) DuoGel Phase 1 Pharmacokinetic Study

Start date: November 1, 2017
Phase: Phase 1
Study type: Interventional

The purpose of this study is describe the safety and single-dose pharmacokinetics of rectally-administered IQP (ImQuest Pharmaceuticals)-0528 (DuoGel) in plasma, rectal tissue biopsies, vaginal tissue biopsies, rectal fluid and cervicovaginal fluid as well as to assess the luminal distribution of IQP-0528 in the rectum. Sixteen healthy volunteers will receive a single rectal dose of DuoGel, followed by blood, tissue and fluid sampling over the following 72 hours.