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Completed Not applicable Interventional Results available

EverFlex Post Approval Study

ClinicalTrials.gov ID: NCT01680835

Public ClinicalTrials.gov record NCT01680835. 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 Oct 23, 2026, 2:14 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

The US StuDy for EvalUating EndovasculaR TreAtments of Lesions in the Superficial Femoral Artery and Proximal Popliteal By usIng the EverfLex NitInol STent System Post Approval Study

Brief summary

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

This post-approval study is designed to confirm the long-term safety and effectiveness of the EverFlex™ Self-Expanding Stent System for the treatment of atherosclerotic superficial femoral artery (SFA) and proximal popliteal arteries.

Study identification

NCT ID
NCT01680835
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Medtronic Endovascular
Industry
Enrollment
108 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
Jan 14, 2013 (Actual)
Primary completion
Oct 23, 2018 (Actual)
Completion
Feb 4, 2019 (Actual)
Last update posted
Dec 26, 2019

2013 – 2019

United States locations

U.S. sites
23
U.S. states
18
U.S. cities
23
Facility City State ZIP Site status
St. Luke's Medical Center Phoenix Arizona 85006 —
Memorial Medical Center Modesto California 95355 —
Sutter Memorial Hospital Sacramento California 95819 —
Christiana Care Health Services Newark Delaware 19713 —
First Coast Cardiovascular Institute, P.A. Jacksonville Florida 32216 —
Augusta Vascular Center Augusta Georgia 30901 —
DuPage Medical Group Downers Grove Illinois 60515 —
Rockford Cardiovascular Associates Rockford Illinois 61107 —
Central Iowa Hospital Corporation Des Moines Iowa 50266 —
Cardiovascular Solutions, LLC Shreveport Louisiana 71103 —
Sparrow Hospital Lansing Michigan 48912 —
Mercy Hospital/Metropolitan Cardiology Consultants Coon Rapids Minnesota 55433 —
Deborah Heart and Lung Center Browns Mills New Jersey 08015 —
Wake Heart Research Raleigh North Carolina 27607 —
Oklahoma Heart Institute Tulsa Oklahoma 74104 —
Lankenau Institute for Medical Research Bryn Mawr Pennsylvania 19010 —
Thomas Jefferson University Philadelphia Pennsylvania 19147 —
Allegheny General Hospital Pittsburgh Pennsylvania 15212 —
Black Hills Cardiovascular Research Rapid City South Dakota 57701 —
Sanford Research Sioux Falls South Dakota 57117 —
Premier Surgical Associates Knoxville Tennessee 37909 —
The University of Texas Health Science Center at San Antonio San Antonio Texas 78229 —
Bellin Memorial Hospital Green Bay Wisconsin 54301 —

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 NCT01680835, 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 Dec 26, 2019 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01680835 live on ClinicalTrials.gov.

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