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NCT00757003 · ClinicalTrials.gov registry record · Phase 3

To Evaluate the Safety and Efficacy for GORE TAG Thoracic Endoprosthesis in the Treatment of Thoracic Aortic Disease

A Phase 3 study, sponsored by Stanford University.

Completed
Registry status
Phase 3
Development phase
100
Enrollment target

NCT00757003: Completed Phase 3 study, sponsored by Stanford University.

NCT00757003 is a Phase 3 study that has completed, run by Stanford University. The registered enrollment target is 100 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT00757003, a Phase 3 study, has completed, sponsored by Stanford University.

COMPLETED
Registry status
Phase 3
Development phase
100 participants
Enrollment target

Study Summary

PURPOSE OF RESEARCH: Endovascular stent-graft repair of aortic pathologies is a minimally-invasive alternative to open surgery that may decrease morbidity and mortality, particularly in high risk patients. Optimal patient selection, based on pathology and anatomy, is being defined. Technically successful implantation requires adequate assessment of pathology and anatomy, and development and execution of novel and delicate procedures that resolve the pathology while minimizing morbidity and mortality.

Primary Outcome

The percentage of participants with technically successful implantation as assessed by the investigator is reported.

Interventions

  • DEVICE Endovascular Stent-graft repair of descending thoracic aorta

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2001-10
Est. Completion 2014-05
Phase Phase 3
Stanford University

1,744 total trials

What the finished NCT00757003 record still lists

NCT00757003 is an interventional study that assigns participants to a tested intervention. The registered 100 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 (87% lower).

The record links to 0 conditions, and to 1 intervention - of which Endovascular Stent-graft repair of descending thoracic aorta is the first listed.

NCT00757003 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00757003 about?

NCT00757003 is a clinical study titled "To Evaluate the Safety and Efficacy for GORE TAG Thoracic Endoprosthesis in the Treatment of Thoracic Aortic Disease". PURPOSE OF RESEARCH: Endovascular stent-graft repair of aortic pathologies is a minimally-invasive alternative to open surgery that may decrease morbidity and mortality, particularly in high risk patients. Optimal patient selection, based on pathology and anatomy, is being defined. Technically succ...

What is the current status of trial NCT00757003?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 100 participants. The study started on 2001-10. Estimated completion is 2014-05.

What interventions are being tested in trial NCT00757003?

The interventions under investigation include: Endovascular Stent-graft repair of descending thoracic aorta (DEVICE).

Who is sponsoring clinical trial NCT00757003?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00757003's enrollment target sits among peer trials

100 1681st of 2000 higher than 288 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 NCT00757003, the US trial registry maintained by the National Library of Medicine. NCT00757003 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.