Clinical trial Recruiting at 1 site Interventional Ages 18 and up

PrEP Linkage With Immediate Medications in the Emergency Department

Official title: HIV Pre-Exposure Prophylaxis (PrEP) Linkage With Immediate Medications in the Emergency Department (PrEP-ED) Study

Run by University of Texas Southwestern Medical Center · NCT07462611 · Data updated 2026-11-12

This study tests starting PrEP right in the Parkland Memorial Hospital ED and linking patients to ongoing PrEP care to see if it increases PrEP uptake in Dallas.

More PrEP trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment250 (estimated)
SponsorUniversity of Texas Southwestern Medical Center
Academic / other
Locations1 site (Dallas, Texas)
StatusRecruiting
StartedApril 8, 2026
Main results expectedOctober 31, 2027
Study endsApril 1, 2028
Registry record updatedJune 2, 2026
Trial IDNCT07462611 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults in Dallas who request PrEP, have a high risk score, a prior STI history, are seeking STI testing, or are referred as likely PrEP candidates and are willing to engage with ongoing PrEP care.

Probably not a fit

Patients who do not seek ongoing PrEP care or do not meet eligibility criteria may not benefit from this approach.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The program is a pilot to increase PrEP awareness and uptake by initiating rapid-start PrEP in the ED and arranging follow-up with a PrEP clinic. A PrEP navigator approaches eligible ED patients, educates them on PrEP options, and obtains consent for participation. If eligible, participants receive a rapid HIV test (if not recently tested) and start PrEP prescriptions with a plan for ongoing care, including long-acting injectable options where appropriate. The study leverages the hospital’s prior HIV prediction tool and navigation program to identify candidates and facilitate linkage to care.

Why it matters

Potential benefit: If successful, the approach could increase timely PrEP initiation and longer-term adherence among individuals at risk for HIV in the ED setting.

How similar studies have gone: Prior ED-based HIV navigation and PrEP initiatives have shown promise for improving initiation and linkage to care in similar settings.

Who can join: the full rules

Show full inclusion / exclusion criteria
Primary study (ED patients):

Inclusion Criteria:

* Able to comprehend and provide signed, written informed consent prior to initiation of study procedures.
* Negative HIV rapid test
* At least one of the following criteria:

  * Requesting PrEP from their ED clinician
  * Score \>75% on the PCCI HIV Prediction Tool
  * Prior bacterial STI diagnosis
  * Seeking STI testing
  * Referred by their ED clinician as someone who otherwise meets a CDC PrEP indication

Exclusion Criteria:

* Known diagnosis of HIV
* Positive HIV rapid test
* Current use of PrEP, which is defined for purposes of this study as use of PrEP in the last 4 weeks
* Known hypersensitivity or allergy to any PrEP modality
* People who do not want to follow with Parkland ID clinic for ongoing PrEP care
* Adults unable to consent, people under the age of 18, women who are known to be pregnant or breast feeding at time of study enrollment, or prisoners

Sub-study subjects (ED clinicians):

Inclusion criteria:

• Clinician in the Parkland ED

Exclusion criteria:

• People under the age of 18 or prisoners.

Where it's running

  • Parkland Health
    Dallas, Texas, United States
    Recruiting

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.