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NCT00371423 · ClinicalTrials.gov registry record · Phase 3

Direct Stenting of TAXUS Liberté™-SR Stent for the Treatment of Patients With de Novo Coronary Artery Lesions

A Phase 3 study, sponsored by Boston Scientific Corporation.

Completed
Registry status
Phase 3
Development phase
247
Enrollment target

NCT00371423: Completed Phase 3 study, sponsored by Boston Scientific Corporation.

NCT00371423 is a Phase 3 study that has completed, run by Boston Scientific Corporation. The registered enrollment target is 247 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

NCT00371423, a Phase 3 study, has completed, sponsored by Boston Scientific Corporation.

COMPLETED
Registry status
Phase 3
Development phase
247 participants
Enrollment target

Study Summary

TAXUS ATLAS Direct Stent is a global, multi-center, single-arm, noninferiority trial comparing results from patients in whom the TAXUS Liberté stent was directly implanted (direct stenting) versus results from patients in whom implantation with the TAXUS Liberté stent was preceded by balloon angioplasty (pre-dilatation). The Control group consists of patients in the main TAXUS ATLAS trial, in which pre-dilatation was mandatory. The primary objective is to compare outcomes of direct stenting with balloon catheter pre-dilatation. The primary hypothesis is that late outcomes with direct stenting of the TAXUS™ Liberté Paclitaxel-Eluting Coronary Stent System will be non-inferior to conventional implantation with balloon catheter pre-dilatation

Interventions

  • DEVICE TAXUS Liberté™-SR

Trial Details

FieldValue
Enrollment Target 247 participants
Start Date 2005-03
Est. Completion 2010-09
Phase Phase 3
Boston Scientific Corporation

280 total trials

What the finished NCT00371423 record still lists

NCT00371423 is an interventional study that assigns participants to a tested intervention. The registered 247 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 1 intervention - of which TAXUS Liberté™-SR is the first listed.

NCT00371423 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00371423 about?

NCT00371423 is a clinical study titled "Direct Stenting of TAXUS Liberté™-SR Stent for the Treatment of Patients With de Novo Coronary Artery Lesions". TAXUS ATLAS Direct Stent is a global, multi-center, single-arm, noninferiority trial comparing results from patients in whom the TAXUS Liberté stent was directly implanted (direct stenting) versus results from patients in whom implantation with the TAXUS Liberté stent was preceded by balloon angiopl...

What is the current status of trial NCT00371423?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 247 participants. The study started on 2005-03. Estimated completion is 2010-09.

What interventions are being tested in trial NCT00371423?

The interventions under investigation include: TAXUS Liberté™-SR (DEVICE).

Who is sponsoring clinical trial NCT00371423?

This trial is sponsored by Boston Scientific Corporation, which has 280 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00371423's enrollment target sits among peer trials

247 1266th of 2000 higher than 734 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 NCT00371423, the US trial registry maintained by the National Library of Medicine. NCT00371423 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.