# A Clinical Study to Assess a Compression Device in Patients With Venous Leg Ulcers

> **NCT02561013** · NA · WITHDRAWN · sponsor: **3M**

## Conditions studied

- Varicose Ulcer

## Interventions

- **DEVICE:** 3M™ Coban™ Custom Fit Compression System
- **DEVICE:** Profore

## Key facts

- **NCT ID:** NCT02561013
- **Lead sponsor:** 3M
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** WITHDRAWN
- **Start date:** 2015-09
- **Primary completion:** 2016-03
- **Final completion:** 2016-03
- **Target enrollment:** 0 (ACTUAL)
- **Why stopped:** Business reasons
- **Last updated:** 2015-11-25


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02561013

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02561013, "A Clinical Study to Assess a Compression Device in Patients With Venous Leg Ulcers". Retrieved via AI Analytics 2026-06-03 from https://api.ai-analytics.org/clinical/NCT02561013. Licensed CC0.

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