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Study details
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Comparison of Dual Antiplatelet Therapy De-escalation by Dose Reduction Versus Switching in Patients Undergoing PCI

University of Florida
NCT IDNCT06821191ClinicalTrials.gov data as of Apr 2026
Phase

Phase 4

Target enrollment

78

Study length

about 1.8 years

Ages

18+

Locations

1 site in FL

What this study is about

This trial is testing whether de-escalating dual antiplatelet therapy (DAPT) by reducing the dose of prasugrel or switching from a more potent P2Y12 inhibitor to clopidogrel provides similar benefits for preventing blood clots after heart procedures. The goal is to compare these two methods of DAPT de-escalation and determine if they are equally effective at preventing bleeding while still protecting against clots.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Prasugrel 5 mg
  • 2.Take clopidogrel 75 mg

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
OralOral

How treatment is administered

Treatment Assignment
Randomized (Open Label)

You are randomly assigned, but you will know your treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

prasugrel, clopidogrel (Antiplatelet; blocks ADP receptors on platelets to prevent aggregation)

Drug routes

oral (Oral Tablet), oral

Body systems

Cardiology / Heart