MedTrace Logo

34mm Cuff Study for Endovascular Repair of Abdominal Aortic Aneurysms

NCT00706394 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 19

Last updated 2021-11-01

Study results available
· View outcomes & findings →

Summary

Study of anatomical fixation with a 34mm proximal extension

Conditions

  • Abdominal Aortic Aneurysm

Interventions

DEVICE

Endologix Powerlink 34 mm stent graft cuff

Endovascular abdominal aortic aneurysm repair

Sponsors & Collaborators

  • Endologix

    lead INDUSTRY

Principal Investigators

  • Edward Y Woo, MD · Hospital at the University of Pennsylvania, Philadelphia, PA 19104, United States

  • O. W. Brown, MD · William Beaumont Hospital, Royal Oak, MI 48073, United States

  • James G. Melton, DO · Oklahoma Cardiovascular Research Group, Oklahoma City, OK 73120, United States

  • Steven H. Tyndall, MD · Nebraska Heart Hospital, Lincoln, NE 68526, United States

  • William M. Moore, MD · Lexington Medical Center, West Columbia, SC 29169, United States

  • Salem George, MD · Baptist Hospital East, Louisville, KY 40207, United States

  • Kerry C. Prewitt, MD · St. Joseph Medical Center, Towson, MD 21204, United States

  • Paul Anain, MD · Sisters of Charity Hospital, Buffalo, NY 14214, United States

  • Robert Beasley, MD · Mount Sinai Medical Center, Miami Beach, FL 33140, United States

  • Barry T. Katzen, MD · Baptist Cardiac and Vascular Institute, Miami, FL 33176, United States

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-08-10
Primary Completion
2013-09-30
Completion
2013-09-30

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00706394 on ClinicalTrials.gov