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NCT04650269 · ClinicalTrials.gov registry record · Phase 4

Implementation of Onsite, Rapid ART Initiation Among People Who Inject Drugs Living With HIV at Syringe Services Program

A Phase 4 study of HIV Infections and Drug Use, sponsored by University of Miami.

Completed
Registry status
Phase 4
Development phase
27
Enrollment target
1
Study location

NCT04650269 is a Phase 4 study of HIV Infections and Drug Use that has completed, run by University of Miami. The registered enrollment target is 27 participants, below the 446-participant average among 542 other HIV Infections trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04650269, a Phase 4 study of HIV Infections and Drug Use, has completed, sponsored by University of Miami.

COMPLETED
Registry status
Phase 4
Development phase
27 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to see if providing HIV medicine right away at the IDEA Syringe Services Program will help the participant start and remain in HIV care, including having no detectable HIV in the participant's blood.

Interventions

  • DRUG Biktarvy 50Mg-200Mg-25Mg Tablet
  • OTHER HIV care

Study Locations (1)

Florida

  • University of Miami - Miami

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2021-03-04
Est. Completion 2023-12-31
Phase Phase 4

Sponsor

University of Miami

721 total trials

What the Registry Record Tells You About NCT04650269

The ClinicalTrials.gov registry entry for NCT04650269 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 27 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 446-participant average among 542 other HIV Infections trials with a reported enrollment target (94% lower). The listed sponsor is University of Miami, which has 721 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with HIV Infections appearing as the primary indexed condition, and to 2 interventions - of which Biktarvy 50Mg-200Mg-25Mg Tablet is the first listed.

NCT04650269 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.

Frequently Asked Questions

What is clinical trial NCT04650269 about?

NCT04650269 is a clinical study titled "Implementation of Onsite, Rapid ART Initiation Among People Who Inject Drugs Living With HIV at Syringe Services Program". The purpose of this study is to see if providing HIV medicine right away at the IDEA Syringe Services Program will help the participant start and remain in HIV care, including having no detectable HIV in the participant's blood.

What is the current status of trial NCT04650269?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 27 participants. The study started on 2021-03-04. Estimated completion is 2023-12-31.

What conditions does trial NCT04650269 study?

This clinical trial studies the following conditions: HIV Infections, Drug Use, Harm Reduction.

What interventions are being tested in trial NCT04650269?

The interventions under investigation include: Biktarvy 50Mg-200Mg-25Mg Tablet (DRUG), HIV care (OTHER).

Who is sponsoring clinical trial NCT04650269?

This trial is sponsored by University of Miami, which has 721 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04650269 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.