# Lutonix or Inpact for tHE tReatment Of fEmeropopliteal Stenosis - Drug Coated Balloon

> **NCT02812966** · NA · TERMINATED · sponsor: **Wake Forest University Health Sciences** · enrollment: 35 (actual)

## Conditions studied

- Peripheral Arterial Disease

## Interventions

- **DEVICE:** Lutonix
- **DEVICE:** IN.PACT

## Key facts

- **NCT ID:** NCT02812966
- **Lead sponsor:** Wake Forest University Health Sciences
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2016-04
- **Primary completion:** 2019-12-02
- **Final completion:** 2019-12-02
- **Target enrollment:** 35 (ACTUAL)
- **Why stopped:** new FDA information regarding drug-coated balloons
- **Last updated:** 2024-10-08


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02812966

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02812966, "Lutonix or Inpact for tHE tReatment Of fEmeropopliteal Stenosis - Drug Coated Balloon". Retrieved via AI Analytics 2026-06-01 from https://api.ai-analytics.org/clinical/NCT02812966. Licensed CC0.

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