Powerlink Bifurcated Stent Graft Long-Term Follow-up Study

ClinicalTrials.gov ID: NCT00543270

Open the official record

This page only displays public information reproduced from the official ClinicalTrials.gov record NCT00543270. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

View official ClinicalTrials.gov record → Back to search

ClinicalTrials.gov public records Last synced Nov 14, 2026, 9:58 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Endologix Powerlink Long-Term Follow-up Study

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Endologix Infrarenal Bifurcated Stent Graft Study

Study identification

NCT ID: NCT00543270
Recruitment status: Completed
Study type: Interventional
Phase: Not applicable
Lead sponsor: Endologix; Industry
Enrollment: 258 participants

Conditions and interventions

Conditions

Abdominal Aortic Aneurysm

Interventions

Powerlink infrarenal bifurcated stent graft delivery system Device
Open Surgery Procedure

Device · Procedure

Eligibility (public fields only)

Age range: 18 Years and older
Sex: All
Healthy volunteers: Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date: Oct 2005 (Type not available)
Primary completion: Nov 2009 (Actual)
Completion: Nov 2009 (Actual)
Last update posted: Oct 5, 2021

2005 – 2009

United States locations

U.S. sites: 14
U.S. states: 13
U.S. cities: 14

Facility	City	State	ZIP	Site status
Arizona Heart Institute	Phoenix	Arizona	85006	—
Harbor-UCLA Medical Center	Torrance	California	90506	—
University of Illinois School of Medicine	Peoria	Illinois	61604	—
SIU School of Medicine	Springfield	Illinois	62702	—
Mercy Hospital	Des Moines	Iowa	50314	—
Mayo Clinic	Rochester	Minnesota	55905	—
Barnes Jewish Hospital	St Louis	Missouri	63110	—
Advanced Vascular Associates	Morristown	New Jersey	07960	—
Cleveland Clinic	Cleveland	Ohio	44195	—
Oklahoma Cardiovascular Research Group	Oklahoma City	Oklahoma	73120	—
University Hospital of Pennsylvania	Philadelphia	Pennsylvania	19104	—
Greenville Hospital System	Greenville	South Carolina	29605	—
Heart Hospital of South Dakota	Sioux Falls	South Dakota	57108	—
Vascular and Transplant Specialists	Norfolk	Virginia	23510	—

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT00543270, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do: No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from: Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh: Last update posted Oct 5, 2021 · Synced Nov 14, 2026