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NCT00054847 · ClinicalTrials.gov registry record · NA

Radial Artery Versus Saphenous Vein Grafts in Coronary Artery Bypass Surgery

A NA study, sponsored by US Department of Veterans Affairs.

Completed
Registry status
NA
Development phase
733
Enrollment target

NCT00054847: Completed NA study, sponsored by US Department of Veterans Affairs.

NCT00054847 is a NA study that has completed, run by US Department of Veterans Affairs. The registered enrollment target is 733 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (48% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00054847, a NA study, has completed, sponsored by US Department of Veterans Affairs.

COMPLETED
Registry status
NA
Development phase
733 participants
Enrollment target

Study Summary

VA patients with coronary artery disease and who have agreed to undergo coronary artery bypass graft surgery would be randomized to receive either radial artery or saphenous vein to the study vessel. The primary outcome variable is graft patency at one year.

Primary Outcome

The primary end point was angiographic graft patency at 1 year after coronary artery bypass surgery, defined as any opacification of distal target by injection of the graft. The window for the 1-year angiogram was 2 to 24 months. This window was chosen to capture early clinically indicated angiograms and late selective angiograms in patients who did not have symptoms. Study grafts that were occluded at 1 week after coronary artery bypass graft surgery were considered occluded at 1 year. One-year

Interventions

  • PROCEDURE saphenous vein graft
  • PROCEDURE radial artery graft

Trial Details

FieldValue
Enrollment Target 733 participants
Start Date 2003-02
Est. Completion 2010-02
Phase NA
US Department of Veterans Affairs

632 total trials

What the finished NCT00054847 record still lists

NCT00054847 is an interventional study that assigns participants to a tested intervention. The registered 733 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (48% lower).

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

NCT00054847 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00054847 about?

NCT00054847 is a clinical study titled "Radial Artery Versus Saphenous Vein Grafts in Coronary Artery Bypass Surgery". VA patients with coronary artery disease and who have agreed to undergo coronary artery bypass graft surgery would be randomized to receive either radial artery or saphenous vein to the study vessel. The primary outcome variable is graft patency at one year.

What is the current status of trial NCT00054847?

This trial is currently completed. It is a NA study. The enrollment target is 733 participants. The study started on 2003-02. Estimated completion is 2010-02.

What interventions are being tested in trial NCT00054847?

The interventions under investigation include: saphenous vein graft (PROCEDURE), radial artery graft (PROCEDURE).

Who is sponsoring clinical trial NCT00054847?

This trial is sponsored by US Department of Veterans Affairs, which has 632 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00054847's enrollment target sits among peer trials

733 145th of 2000 higher than 1,856 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 NCT00054847, the US trial registry maintained by the National Library of Medicine. NCT00054847 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.