# Α Pre CE-Marking Study Using the Rontis Drug Coated Balloon for Treatment of Lesions in Femoropopliteal Arteries

> **NCT04821388** · NA · UNKNOWN · sponsor: **Rontis Hellas SA** · enrollment: 30 (actual)

## Conditions studied

- Peripheral Artery Disease (PAD)

## Interventions

- **DEVICE:** Rontis DCB

## Key facts

- **NCT ID:** NCT04821388
- **Lead sponsor:** Rontis Hellas SA
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2019-01-11
- **Primary completion:** 2020-08-30
- **Final completion:** 2021-08-30
- **Target enrollment:** 30 (ACTUAL)
- **Last updated:** 2021-03-29

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04821388

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04821388, "Α Pre CE-Marking Study Using the Rontis Drug Coated Balloon for Treatment of Lesions in Femoropopliteal Arteries". Retrieved via AI Analytics 2026-06-01 from https://api.ai-analytics.org/clinical/NCT04821388. Licensed CC0.

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