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NCT02448550 · ClinicalTrials.gov registry record · Phase 3

Comparison of Anticoagulation for All-comers Undergoing Percutaneous Coronary Revascularization Trial

A Phase 3 study, sponsored by Kaiser Permanente.

Terminated
Registry status
Phase 3
Development phase
250
Enrollment target

NCT02448550: Clinical Trial Phase 3 study, sponsored by Kaiser Permanente.

NCT02448550 is a Phase 3 study that was terminated before completion, run by Kaiser Permanente. The registered enrollment target is 250 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (68% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02448550, a Phase 3 study, was terminated before completion, sponsored by Kaiser Permanente.

TERMINATED
Registry status
Phase 3
Development phase
250 participants
Enrollment target

Study Summary

The purpose of this trial is to determine whether bivalirudin is non-inferior to unfractionated heparin in patients with stable angina, unstable angina, or non-ST segment elevation myocardial infarction undergoing percutaneous coronary intervention.

Interventions

  • DRUG Bivalirudin
  • DRUG Unfractionated heparin

Trial Details

FieldValue
Enrollment Target 250 participants
Start Date 2015-05
Est. Completion 2016-06-16
Phase Phase 3
Kaiser Permanente

294 total trials

Why NCT02448550 stopped before completion

NCT02448550 is an interventional study that assigns participants to a tested intervention. The registered 250 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (68% lower).

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

NCT02448550 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02448550 about?

NCT02448550 is a clinical study titled "Comparison of Anticoagulation for All-comers Undergoing Percutaneous Coronary Revascularization Trial". The purpose of this trial is to determine whether bivalirudin is non-inferior to unfractionated heparin in patients with stable angina, unstable angina, or non-ST segment elevation myocardial infarction undergoing percutaneous coronary intervention.

What is the current status of trial NCT02448550?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 250 participants. The study started on 2015-05. Estimated completion is 2016-06-16.

What interventions are being tested in trial NCT02448550?

The interventions under investigation include: Bivalirudin (DRUG), Unfractionated heparin (DRUG).

Who is sponsoring clinical trial NCT02448550?

This trial is sponsored by Kaiser Permanente, which has 294 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02448550's enrollment target sits among peer trials

250 1249th of 2000 higher than 735 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT02448550, the US trial registry maintained by the National Library of Medicine. NCT02448550 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.