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NCT01793597 · ClinicalTrials.gov registry record

Platelet Reactivity After CABG

A clinical trial, sponsored by University of Vermont.

Completed
Registry status
18
Enrollment target

NCT01793597 is a clinical trial that has completed, run by University of Vermont. The registered enrollment target is 18 participants.

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The verdict

NCT01793597 has completed, sponsored by University of Vermont.

COMPLETED
Registry status
18 participants
Enrollment target

Study Summary

Patients who have a heart attack are regularly treated with either clopidogrel or ticagrelor. In a large clinical trial, treatment with ticagrelor before coronary bypass surgery (CABG) was associated with a lower risk of death than treatment with clopidogrel. The reason for this difference cannot be explained on the basis of the study. One possible explanation is that the reversible binding of ticagrelor is advantageous because when new platelets are released, they are inhibited by the drug. Because clopidogrel binds irreversibly it cannot redistribute. The investigators will recruit patients who are scheduled for surgery after an acute coronary syndrome who have been treated with either ticagrelor or clopidogrel. After the patient provides informed consent, the investigators will review their medical record,record information and on the day after surgery the investigators will take one sample of blood. That blood will be analyzed for evidence of platelet activation (platelet microparticles, and platelet-leukocyte aggregates), the reactivity of young platelets, and the concentration of inflammatory cytokines. The investigators hypothesize that the evidence of platelet activation (platelet microparticles and platelet-leukocyte aggregates) and the reactivity of young platelets will be less in patients who have been treated previously with ticagrelor.

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2013-05
Est. Completion 2015-09

Sponsor

University of Vermont

162 total trials

What the Registry Record Tells You About NCT01793597

The ClinicalTrials.gov registry entry for NCT01793597 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Vermont, which has 162 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 0 interventions.

NCT01793597 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01793597 about?

NCT01793597 is a clinical study titled "Platelet Reactivity After CABG". Patients who have a heart attack are regularly treated with either clopidogrel or ticagrelor. In a large clinical trial, treatment with ticagrelor before coronary bypass surgery (CABG) was associated with a lower risk of death than treatment with clopidogrel. The reason for this difference cannot be...

What is the current status of trial NCT01793597?

This trial is currently completed. The enrollment target is 18 participants. The study started on 2013-05. Estimated completion is 2015-09.

Who is sponsoring clinical trial NCT01793597?

This trial is sponsored by University of Vermont, which has 162 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.