# Compression Device Safety Study

> **NCT00732823** · PHASE2 · COMPLETED · sponsor: **ConvaTec Inc.** · enrollment: 16 (actual)

## Conditions studied

- Venous Insufficiency

## Interventions

- **DEVICE:** Placebo - No device worn
- **DEVICE:** Prototype device(unnamed)-A battery operated inflatable pneumatic cuffs
- **DEVICE:** Prototype device(unnamed)-A battery operated inflatable pneumatic cuffs
- **DEVICE:** Prototype device(unnamed)-A battery operated inflatable pneumatic cuffs

## Key facts

- **NCT ID:** NCT00732823
- **Lead sponsor:** ConvaTec Inc.
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE2
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2005-07
- **Primary completion:** 2005-10
- **Final completion:** 2005-10
- **Target enrollment:** 16 (ACTUAL)
- **Last updated:** 2008-10-31

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00732823

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00732823, "Compression Device Safety Study". Retrieved via AI Analytics 2026-06-03 from https://api.ai-analytics.org/clinical/NCT00732823. Licensed CC0.

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