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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 Jun 25, 2026, 8:08 PM 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

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

Interventions

  • EverFlex™ Self-Expanding Peripheral Stent System Device

Device

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 13, 2013
Primary completion
Oct 22, 2018
Completion
Feb 3, 2019
Last update posted
Dec 25, 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 25, 2019 · Synced Jun 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01680835 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →