Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01742117 · ClinicalTrials.gov registry record · Phase 4

Tailored Antiplatelet Therapy Following PCI

A Phase 4 study, sponsored by Mayo Clinic.

Completed
Registry status
Phase 4
Development phase
5,276
Enrollment target

NCT01742117: Completed Phase 4 study, sponsored by Mayo Clinic.

NCT01742117 is a Phase 4 study that has completed, run by Mayo Clinic. The registered enrollment target is 5,276 participants, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (919% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT01742117, a Phase 4 study, has completed, sponsored by Mayo Clinic.

COMPLETED
Registry status
Phase 4
Development phase
5,276 participants
Enrollment target

Study Summary

Clopidogrel is an anti-platelet medication approved by the U.S. Federal Drug Administration (FDA) for use in patients who undergo Percutaneous Coronary Intervention (PCI) with coronary stent implantation. Anti-platelet medications work to prevent blood clots from forming. Some studies have suggested that patients who have a certain genetic liver enzyme abnormality (known as cytochrome P450 2C19 \[CYP2C19\] \*2 or \*3 allele) may have a reduced ability to activate clopidogrel, and therefore may have a lowered response to clopidogrel. It is thought that perhaps people who have a coronary stent procedure may have this genetic liver enzyme abnormality. There is a research genetic test available to determine whether or not someone has this genetic liver enzyme abnormality. Ticagrelor, is a newer anti-platelet drug that is not dependent on the CYP2C19 liver enzyme for its activation and hence in poor clopidogrel metabolizers, alternative drugs like Ticagrelor have been recommended for use as an anti-platelet agent after PCI. The purpose of this study is to determine if genetic testing can identify the best anti-platelet therapy, for patients who undergo a coronary stent placement and do not activate clopidogrel very well.

Primary Outcome

Number of subjects who experienced major adverse cardiovascular event as defined as cardiovascular death, myocardial infarction, stroke, severe recurrent ischemia, and stent thrombosis in subjects identified as CPY2C19 LOF carriers by TaqMan.

Interventions

  • DRUG Clopidogrel
  • DRUG Ticagrelor

Trial Details

FieldValue
Enrollment Target 5,276 participants
Start Date 2013-05
Est. Completion 2020-10-31
Phase Phase 4
Mayo Clinic

2,844 total trials

What the finished NCT01742117 record still lists

NCT01742117 is an interventional study that assigns participants to a tested intervention. Its 5,276 participants enrollment target places it among the larger protocols in the corpus, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (919% higher).

The record links to 0 conditions, and to 2 interventions - of which Clopidogrel is the first listed.

NCT01742117 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01742117 about?

NCT01742117 is a clinical study titled "Tailored Antiplatelet Therapy Following PCI". Clopidogrel is an anti-platelet medication approved by the U.S. Federal Drug Administration (FDA) for use in patients who undergo Percutaneous Coronary Intervention (PCI) with coronary stent implantation. Anti-platelet medications work to prevent blood clots from forming. Some studies have suggested...

What is the current status of trial NCT01742117?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 5,276 participants. The study started on 2013-05. Estimated completion is 2020-10-31.

What interventions are being tested in trial NCT01742117?

The interventions under investigation include: Clopidogrel (DRUG), Ticagrelor (DRUG).

Who is sponsoring clinical trial NCT01742117?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01742117's enrollment target sits among peer trials

5,276 16th of 2000 higher than 1,985 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

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

Similar enrollment target

  • NCT06506344 · 5,250 participants · NA

    Syncing Screening and Services for Suicide Prevention Across Health and Justice Systems

  • NCT05373771 · 5,328 participants · NA

    Sickle Cell Improvement: Enhancing Care in the Emergency Department

  • NCT05836987 · 5,350 participants · Phase 3

    The Rhythm Evaluation for AntiCoagulaTion With Continuous Monitoring of Atrial Fibrillation

  • NCT05989308 · 5,200 participants · NA

    MyChart Proxy Outreach to Parents (MyPOP)

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01742117, the US trial registry maintained by the National Library of Medicine. NCT01742117 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.