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NCT01852162 · ClinicalTrials.gov registry record · NA

Pharmacodynamic Effects of Dabigatran in Patients on Dual Antiplatelet Therapy

A NA study, sponsored by University of Florida.

Completed
Registry status
NA
Development phase
35
Enrollment target

NCT01852162: Completed NA study, sponsored by University of Florida.

NCT01852162 is a NA study that has completed, run by University of Florida. The registered enrollment target is 35 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01852162, a NA study, has completed, sponsored by University of Florida.

COMPLETED
Registry status
NA
Development phase
35 participants
Enrollment target

Study Summary

Dual antiplatelet therapy consisting of aspirin and clopidogrel is the cornerstone of treatment for prevention of atherothrombotic events in patients with coronary artery disease (CAD) undergoing percutaneous coronary interventions (PCI). Many patients on dual antiplatelet therapy in this setting may be affected by other thromboembolic conditions, in particular atrial fibrillation, therefore having an indication to also receive oral anticoagulation for stroke prevention. Thus, a considerable percentage of patients are under "triple therapy" which consists of aspirin plus clopidogrel plus an oral anticoagulant. The ever raising population with CAD warranting triple therapy and the growing number of patients being treated with dabigatran underscores the importance of understanding the pharmacodynamic effects of this treatment regimen.

Primary Outcome

TRAP-induced platelet aggregation measured by light transmittance aggregometry (LTA) was similar between groups

Interventions

  • DRUG Placebo
  • DRUG Dabigatran

Trial Details

FieldValue
Enrollment Target 35 participants
Start Date 2012-02
Est. Completion 2014-02
Phase NA
University of Florida

1,106 total trials

What the finished NCT01852162 record still lists

NCT01852162 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 35 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

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

NCT01852162 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01852162 about?

NCT01852162 is a clinical study titled "Pharmacodynamic Effects of Dabigatran in Patients on Dual Antiplatelet Therapy". Dual antiplatelet therapy consisting of aspirin and clopidogrel is the cornerstone of treatment for prevention of atherothrombotic events in patients with coronary artery disease (CAD) undergoing percutaneous coronary interventions (PCI). Many patients on dual antiplatelet therapy in this setting ma...

What is the current status of trial NCT01852162?

This trial is currently completed. It is a NA study. The enrollment target is 35 participants. The study started on 2012-02. Estimated completion is 2014-02.

What interventions are being tested in trial NCT01852162?

The interventions under investigation include: Placebo (DRUG), Dabigatran (DRUG).

Who is sponsoring clinical trial NCT01852162?

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

How this trial's enrollment target compares

Where NCT01852162's enrollment target sits among peer trials

35 1564th of 2000 higher than 431 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT01852162, the US trial registry maintained by the National Library of Medicine. NCT01852162 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.