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NCT00131872 · ClinicalTrials.gov registry record · Phase 2

Study to Evaluate the Performance and Safety of Expedial and Compare it to Expanded Polytetrafluoroethylene (ePTFE) Vascular Access Grafts

A Phase 2 study, sponsored by LeMaitre Vascular.

Terminated
Registry status
Phase 2
Development phase
172
Enrollment target

NCT00131872: Clinical Trial Phase 2 study, sponsored by LeMaitre Vascular.

NCT00131872 is a Phase 2 study that was terminated before completion, run by LeMaitre Vascular. The registered enrollment target is 172 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (29% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00131872, a Phase 2 study, was terminated before completion, sponsored by LeMaitre Vascular.

TERMINATED
Registry status
Phase 2
Development phase
172 participants
Enrollment target

Study Summary

The purpose of this study is to establish the substantial equivalence of Expedial and ePTFE grafts for effectiveness in maintaining primary or assisted primary patency.

Interventions

  • DEVICE Expedial Vascular Access Graft

Trial Details

FieldValue
Enrollment Target 172 participants
Start Date 2004-03
Est. Completion 2006-11
Phase Phase 2
LeMaitre Vascular

2 total trials

Why NCT00131872 stopped before completion

NCT00131872 is an interventional study that assigns participants to a tested intervention. The registered 172 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (29% higher).

The record links to 0 conditions, and to 1 intervention - of which Expedial Vascular Access Graft is the first listed.

NCT00131872 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00131872 about?

NCT00131872 is a clinical study titled "Study to Evaluate the Performance and Safety of Expedial and Compare it to Expanded Polytetrafluoroethylene (ePTFE) Vascular Access Grafts". The purpose of this study is to establish the substantial equivalence of Expedial and ePTFE grafts for effectiveness in maintaining primary or assisted primary patency.

What is the current status of trial NCT00131872?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 172 participants. The study started on 2004-03. Estimated completion is 2006-11.

What interventions are being tested in trial NCT00131872?

The interventions under investigation include: Expedial Vascular Access Graft (DEVICE).

Who is sponsoring clinical trial NCT00131872?

This trial is sponsored by LeMaitre Vascular, which has 2 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00131872's enrollment target sits among peer trials

172 397th of 2000 higher than 1,603 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00131872, the US trial registry maintained by the National Library of Medicine. NCT00131872 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.