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NCT01343667 · ClinicalTrials.gov registry record · NA

GORE Flow Reversal System and GORE Embolic Filter Extension Study

A NA study, sponsored by W.L.Gore & Associates.

Completed
Registry status
NA
Development phase
1,397
Enrollment target

NCT01343667: Completed NA study, sponsored by W.L.Gore & Associates.

NCT01343667 is a NA study that has completed, run by W.L.Gore & Associates. The registered enrollment target is 1,397 participants, roughly in line with the 1,404-participant average among 58,714 other NA trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01343667, a NA study, has completed, sponsored by W.L.Gore & Associates.

COMPLETED
Registry status
NA
Development phase
1,397 participants
Enrollment target

Study Summary

The objective of this study is to provide an ongoing evaluation of clinical outcomes associated with the GORE Flow Reversal System and the GORE Embolic Filter when used for embolic protection during carotid artery stenting.

Primary Outcome

Major Adverse Events include death, stroke and myocardial infarction

Interventions

  • DEVICE Gore Flow Reversal System
  • DEVICE Gore Embolic Filter

Trial Details

FieldValue
Enrollment Target 1,397 participants
Start Date 2011-04
Est. Completion 2014-01
Phase NA
W.L.Gore & Associates

53 total trials

What the finished NCT01343667 record still lists

NCT01343667 is an interventional study that assigns participants to a tested intervention. Its 1,397 participants enrollment target places it among the larger protocols in the corpus, roughly in line with the 1,404-participant average among 58,714 other NA trials with a reported enrollment target.

The record links to 0 conditions, and to 2 interventions - of which Gore Flow Reversal System is the first listed.

NCT01343667 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01343667 about?

NCT01343667 is a clinical study titled "GORE Flow Reversal System and GORE Embolic Filter Extension Study". The objective of this study is to provide an ongoing evaluation of clinical outcomes associated with the GORE Flow Reversal System and the GORE Embolic Filter when used for embolic protection during carotid artery stenting.

What is the current status of trial NCT01343667?

This trial is currently completed. It is a NA study. The enrollment target is 1,397 participants. The study started on 2011-04. Estimated completion is 2014-01.

What interventions are being tested in trial NCT01343667?

The interventions under investigation include: Gore Flow Reversal System (DEVICE), Gore Embolic Filter (DEVICE).

Who is sponsoring clinical trial NCT01343667?

This trial is sponsored by W.L.Gore & Associates, which has 53 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01343667's enrollment target sits among peer trials

1,397 73rd of 2000 higher than 1,928 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 NCT01343667, the US trial registry maintained by the National Library of Medicine. NCT01343667 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.