# EverFlex Post Approval Study

> **NCT01680835** · NA · COMPLETED · sponsor: **Medtronic Endovascular** · enrollment: 108 (actual)

## Conditions studied

- Peripheral Arterial Disease
- Lower Extremity Arterial Disease

## Interventions

- **DEVICE:** EverFlex™ Self-Expanding Peripheral Stent System

## Key facts

- **NCT ID:** NCT01680835
- **Lead sponsor:** Medtronic Endovascular
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2013-01-14
- **Primary completion:** 2018-10-23
- **Final completion:** 2019-02-04
- **Target enrollment:** 108 (ACTUAL)
- **Last updated:** 2019-12-26


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01680835

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01680835, "EverFlex Post Approval Study". Retrieved via AI Analytics 2026-05-27 from https://api.ai-analytics.org/clinical/NCT01680835. Licensed CC0.

---

*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*