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Completed Not applicable Interventional Results available

Percutaneous Endovascular Aneurysm Repair (PEVAR) Trial

ClinicalTrials.gov ID: NCT01070069

Public ClinicalTrials.gov record NCT01070069. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 4:18 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Prospective, Multicenter, Randomized Controlled Trial of Endovascular Aneurysm Repair Using a Bilateral Percutaneous Approach (PEVAR) vs. Standard Approach (SEVAR) Using the IntuiTrak Endovascular AAA Delivery System and the Prostar XL or Perclose ProGlide Suture-Mediated Closure System

Brief summary

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

To determine the safety and effectiveness of PEVAR.

Study identification

NCT ID
NCT01070069
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Endologix
Industry
Enrollment
192 participants

Conditions and interventions

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
Apr 12, 2010
Primary completion
Mar 8, 2012
Completion
Sep 4, 2012
Last update posted
Jun 6, 2022

2010 – 2012

United States locations

U.S. sites
20
U.S. states
12
U.S. cities
18
Facility City State ZIP Site status
Loma Linda VA Medical Center Loma Linda California 92357
VA San Diego San Diego California 92161
Holy Cross Medical Center Fort Lauderdale Florida 33308
VA Gainesville Gainesville Florida 32608
VA Miami Miami Florida 33125
Baptist Cardiac and Vascular Institute Miami Florida 33176
Northwestern University Chicago Illinois 60611
Mercy Hospital Chicago Illinois 60616
Forrest General Hospital Hattiesburg Mississippi 39401
Dartmouth-Hitchcock Medical Center Lebanon New Hampshire 03756
Mission Hospital Asheville North Carolina 28801
Cleveland Clinic Cleveland Ohio 44195
Lake Health Willoughby Ohio 44094
Oklahoma Heart Hospital Oklahoma City Oklahoma 93120
North Central Heart Hospital Sioux Falls South Dakota 57108
Dallas VA Medical Center Dallas Texas 75216
St. Luke's Hospital at Texas Heart Institute Houston Texas 77030
University of Virginia Charlottesville Virginia 22903
Inova Fairfax Falls Church Virginia 22042
University of Wisconsin Madison Wisconsin 53792

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 NCT01070069, 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 Jun 6, 2022 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01070069 live on ClinicalTrials.gov.

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