PrEP on the spot: HIV prevention delivered at syringe services shows promise
NCT ID NCT04782180
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This pilot study tested whether giving the HIV prevention pill Descovy (PrEP) right at a syringe services program helps people stay HIV-negative. 90 adults who use the syringe program and tested negative for HIV took part. Researchers measured drug levels in blood to see if participants were taking the pills regularly. The goal is to make PrEP easier to access for people at high risk.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Descovy (emtricitabine/tenofovir alafenamide) tablet
- What this could lead to
- If successful, this approach could make it easier for people who use drugs to get HIV prevention medication, reducing new infections.
- What could go wrong
- This is a small pilot study (90 people) without a comparison group, so results may not apply broadly. Adherence to daily pills can be challenging.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
90 people
The number who actually took part.
- Started
-
Feb 2022
- Finished
-
Nov 2024
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. over the age of 18 2. speak either English or Spanish 3. ability to provide informed consent 4. currently enrolled in the syringe services program 5. have a negative HIV rapid test result 6. estimated creatinine clearance \> 30 ml/minute Exclusion Criteria: 1. do not meet the above criteria of inclusion 2. decline to participate 3. test positive for HIV via rapid test 4. are pregnant or plan on becoming pregnant 5. have symptoms acute HIV. 6. Any other comorbidities that at the discretion of the investigator would prevent the participant from participating in the study.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for HIV are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University of Miami
Miami, Florida, 33136, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can exercise boost brain and body health during opioid treatment?
- Can 'Queen Mothers' bring HIV testing to the doorstep?
- Scientists map HIV's hiding spots in early infection
- Can local clinics keep more people with HIV in care?
- Can a phone call keep HIV-Positive mothers and babies on track?
- Can a phone app and a health worker ease depression in rural HIV care?