# This Study Will Collect Clinical and Patient Reported Satisfaction Data From Males Requiring Urine Output Management Overnight in the Home Setting.

> **NCT06850259** · NA · COMPLETED · sponsor: **C. R. Bard** · enrollment: 15 (actual)

## Conditions studied

- Urinary Incontinence

## Interventions

- **DEVICE:** PureWick™ System
- **DEVICE:** UltraFlex™ Self-Adhering Male External Catheter

## Key facts

- **NCT ID:** NCT06850259
- **Lead sponsor:** C. R. Bard
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2025-03-21
- **Primary completion:** 2025-06-15
- **Final completion:** 2025-06-15
- **Target enrollment:** 15 (ACTUAL)
- **Last updated:** 2025-06-29

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06850259

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06850259, "This Study Will Collect Clinical and Patient Reported Satisfaction Data From Males Requiring Urine Output Management Overnight in the Home Setting.". Retrieved via AI Analytics 2026-07-07 from https://api.ai-analytics.org/clinical/NCT06850259. Licensed CC0.

---

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