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.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 250 (estimated) |
| Sponsor | University of Texas Southwestern Medical Center Academic / other |
| Locations | 1 site (Dallas, Texas) |
| Status | Recruiting |
| Started | April 8, 2026 |
| Main results expected | October 31, 2027 |
| Study ends | April 1, 2028 |
| Registry record updated | June 2, 2026 |
| Trial ID | NCT07462611 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
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Parkland Health
Dallas, Texas, United States Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.