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NCT00314275 · ClinicalTrials.gov registry record · NA

The ENDEAVOR Pharmacokinetic (PK) Registry: The Medtronic Endeavor Drug Eluting Coronary Stent System

A NA study, sponsored by Medtronic Vascular.

Completed
Registry status
NA
Development phase
43
Enrollment target

NCT00314275: Completed NA study, sponsored by Medtronic Vascular.

NCT00314275 is a NA study that has completed, run by Medtronic Vascular. The registered enrollment target is 43 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00314275, a NA study, has completed, sponsored by Medtronic Vascular.

COMPLETED
Registry status
NA
Development phase
43 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the pharmacokinetics (PK) and safety associated with ABT-578 administered using the Medtronic Endeavor Drug Eluting Coronary Stent system in the treatment of single de novo lesions in native coronary arteries between 2.5 - 3.5 mm in diameter.

Interventions

  • DEVICE Endeavor
  • DEVICE Coronary Artery Stenting

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2006-01
Est. Completion 2011-08
Phase NA
Medtronic Vascular

26 total trials

What the finished NCT00314275 record still lists

NCT00314275 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 43 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

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

NCT00314275 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00314275 about?

NCT00314275 is a clinical study titled "The ENDEAVOR Pharmacokinetic (PK) Registry: The Medtronic Endeavor Drug Eluting Coronary Stent System". The purpose of this study is to evaluate the pharmacokinetics (PK) and safety associated with ABT-578 administered using the Medtronic Endeavor Drug Eluting Coronary Stent system in the treatment of single de novo lesions in native coronary arteries between 2.5 - 3.5 mm in diameter.

What is the current status of trial NCT00314275?

This trial is currently completed. It is a NA study. The enrollment target is 43 participants. The study started on 2006-01. Estimated completion is 2011-08.

What interventions are being tested in trial NCT00314275?

The interventions under investigation include: Endeavor (DEVICE), Coronary Artery Stenting (DEVICE).

Who is sponsoring clinical trial NCT00314275?

This trial is sponsored by Medtronic Vascular, which has 26 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00314275's enrollment target sits among peer trials

43 1435th of 2000 higher than 565 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 NCT00314275, the US trial registry maintained by the National Library of Medicine. NCT00314275 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.