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NCT00781573 · ClinicalTrials.gov registry record · NA

Study of Optimal Clopidogrel Duration in Patients Receiving Drug Eluting Stents (SCORE Trial)

A NA study, sponsored by North Texas Veterans Healthcare System.

Completed
Registry status
NA
Development phase
167
Enrollment target

NCT00781573 is a NA study that has completed, run by North Texas Veterans Healthcare System. The registered enrollment target is 167 participants.

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The verdict

NCT00781573, a NA study, has completed, sponsored by North Texas Veterans Healthcare System.

COMPLETED
Registry status
NA
Development phase
167 participants
Enrollment target

Study Summary

Although the optimal duration of clopidogrel (an anti-platelet agent) therapy has been established after bare metal stent implantation in the blood vessels of the heart, there is lack of consensus regarding the optimal duration of therapy after implantation of a drug eluting stents (DES). Current American College of Cardiology guidelines recommend clopidogrel use for at least one year in the absence of contraindications after DES implantation, while recognizing that the optimal duration remains unknown. While an extended clopidogrel therapy (that is beyond the current 1 year recommendation) may increase bleeding complication, it may reduce the rates of adverse cardiovascular events like heart attacks and repeat revascularization procedures. A clinical trial which randomizes patients with an uneventful one year course after a DES implantation, to an additional year of clopidogrel and aspirin therapy versus aspirin alone, will be able to answer the important question about the role of extended (2y) dual anti-platelet therapy with clopidogrel and aspirin after DES implants. The investigators hypothesize that clopidogrel discontinuation at 1 year post-DES implantation is associated with an increase in cardiovascular events during the one year of follow-up period.

Interventions

  • DRUG Clopidogrel

Trial Details

FieldValue
Enrollment Target 167 participants
Start Date 2008-09-11
Est. Completion 2014-03-03
Phase NA

What the Registry Record Tells You About NCT00781573

The ClinicalTrials.gov registry entry for NCT00781573 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 167 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is North Texas Veterans Healthcare System, which has 23 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Clopidogrel is the first listed.

NCT00781573 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00781573 about?

NCT00781573 is a clinical study titled "Study of Optimal Clopidogrel Duration in Patients Receiving Drug Eluting Stents (SCORE Trial)". Although the optimal duration of clopidogrel (an anti-platelet agent) therapy has been established after bare metal stent implantation in the blood vessels of the heart, there is lack of consensus regarding the optimal duration of therapy after implantation of a drug eluting stents (DES). Current Am...

What is the current status of trial NCT00781573?

This trial is currently completed. It is a NA study. The enrollment target is 167 participants. The study started on 2008-09-11. Estimated completion is 2014-03-03.

What interventions are being tested in trial NCT00781573?

The interventions under investigation include: Clopidogrel (DRUG).

Who is sponsoring clinical trial NCT00781573?

This trial is sponsored by North Texas Veterans Healthcare System, which has 23 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.