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NCT00356135 · ClinicalTrials.gov registry record · Phase 2

Effect of Prasugrel on Platelets After One Week in Patients Already Taking Clopidogrel After a Cardiac Event

A Phase 2 study, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 2
Development phase
139
Enrollment target

NCT00356135: Completed Phase 2 study, sponsored by Eli Lilly and Company.

NCT00356135 is a Phase 2 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 139 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00356135, a Phase 2 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 2
Development phase
139 participants
Enrollment target

Study Summary

This study will compare the effect of a prasugrel 10-mg maintenance dose with a clopidogrel 75-mg maintenance dose on platelet activity, approximately 1 week after the first dose of study drug, in subjects who have been taking clopidogrel 75 mg daily following a percutaneous coronary intervention (PCI) with placement of a stent, performed to treat acute coronary syndrome (ACS).

Primary Outcome

Maximum platelet aggregation (MPA) to 20 micromolar adenosine diphosphase (ADP) as measured with light transmittance aggregometry (LTA).

Interventions

  • DRUG clopidogrel
  • DRUG prasugrel 10 mg
  • DRUG prasugrel placebo
  • DRUG prasugrel 60 mg
  • DRUG clopidogrel placebo

Trial Details

FieldValue
Enrollment Target 139 participants
Start Date 2006-07
Est. Completion 2008-12
Phase Phase 2
Eli Lilly and Company

1,341 total trials

What the finished NCT00356135 record still lists

NCT00356135 is an interventional study that assigns participants to a tested intervention. The registered 139 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.

The record links to 0 conditions, and to 5 interventions - of which clopidogrel is the first listed.

NCT00356135 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00356135 about?

NCT00356135 is a clinical study titled "Effect of Prasugrel on Platelets After One Week in Patients Already Taking Clopidogrel After a Cardiac Event". This study will compare the effect of a prasugrel 10-mg maintenance dose with a clopidogrel 75-mg maintenance dose on platelet activity, approximately 1 week after the first dose of study drug, in subjects who have been taking clopidogrel 75 mg daily following a percutaneous coronary intervention (P...

What is the current status of trial NCT00356135?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 139 participants. The study started on 2006-07. Estimated completion is 2008-12.

What interventions are being tested in trial NCT00356135?

The interventions under investigation include: clopidogrel (DRUG), prasugrel 10 mg (DRUG), prasugrel placebo (DRUG), prasugrel 60 mg (DRUG), clopidogrel placebo (DRUG).

Who is sponsoring clinical trial NCT00356135?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00356135's enrollment target sits among peer trials

139 525th of 2000 higher than 1,476 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

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Source: ClinicalTrials.gov NCT00356135, the US trial registry maintained by the National Library of Medicine. NCT00356135 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.