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NCT06588595 · ClinicalTrials.gov registry record · Phase 4

The Switching Antiplatelet-9 (SWAP-9) Study

A Phase 4 study of Coronary Arterial Disease (CAD), sponsored by University of Florida.

Recruiting
Registry status
Phase 4
Development phase
90
Enrollment target
1
Study location

NCT06588595: Recruiting Phase 4 study of Coronary Arterial Disease (CAD), sponsored by University of Florida.

NCT06588595 is a Phase 4 study of Coronary Arterial Disease (CAD) that is actively recruiting participants, run by University of Florida. The registered enrollment target is 90 participants, below the 3,061-participant average among 5 other Coronary Arterial Disease (CAD) trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06588595, a Phase 4 study of Coronary Arterial Disease (CAD), is actively recruiting participants, sponsored by University of Florida.

RECRUITING
Registry status
Phase 4
Development phase
90 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to compare the pharmacodynamic effects of ABCD-GENE guided vs. unguided de-escalation strategies among patients on dual antiplatelet therapy (DAPT) following percutaneous coronary intervention (PCI).

Primary Outcome

Comparison of PRU determined by VerifyNow between ABCD-GENE-guided de-escalation vs. unguided de-escalation.

Interventions

  • DRUG Prasugrel/Ticagrelor monotherapy or aspirin plus clopidogrel
  • DRUG Aspirin plus clopidogrel

Study Locations (1)

Florida

  • University of Florida - Jacksonville

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2024-11-01
Est. Completion 2027-02-28
Phase Phase 4
University of Florida

1,106 total trials

What NCT06588595 shows while recruiting

NCT06588595 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 90 participants, a relatively small participant target, below the 3,061-participant average among 5 other Coronary Arterial Disease (CAD) trials with a reported enrollment target (97% lower).

The record links to 1 condition, with Coronary Arterial Disease (CAD) appearing as the primary indexed condition, and to 2 interventions - of which Prasugrel/Ticagrelor monotherapy or aspirin plus clopidogrel is the first listed.

NCT06588595 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT06588595 about?

NCT06588595 is a clinical study titled "The Switching Antiplatelet-9 (SWAP-9) Study". The purpose of this study is to compare the pharmacodynamic effects of ABCD-GENE guided vs. unguided de-escalation strategies among patients on dual antiplatelet therapy (DAPT) following percutaneous coronary intervention (PCI).

What is the current status of trial NCT06588595?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 90 participants. The study started on 2024-11-01. Estimated completion is 2027-02-28.

What conditions does trial NCT06588595 study?

This clinical trial studies the following conditions: Coronary Arterial Disease (CAD).

What interventions are being tested in trial NCT06588595?

The interventions under investigation include: Prasugrel/Ticagrelor monotherapy or aspirin plus clopidogrel (DRUG), Aspirin plus clopidogrel (DRUG).

Who is sponsoring clinical trial NCT06588595?

This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06588595 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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Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

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Source: ClinicalTrials.gov NCT06588595, the US trial registry maintained by the National Library of Medicine. NCT06588595 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.