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ClinicalTrials.gov record
Completed Not applicable Interventional

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

ClinicalTrials.gov ID: NCT06666426

Public ClinicalTrials.gov record NCT06666426. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 6:28 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Controlled Trial on the Safety, Efficacy, and Patient Reported Experience Comparing PureWick™ System With an Established Comparator Overnight in the Home Setting (PUREST)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This post-market study will assess the performance of and user experience with the PureWick™ System in a home setting. The study will also observe safety of the study device and collect information from participants about their quality of life before and after using the device.

Study identification

NCT ID
NCT06666426
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
C. R. Bard
Industry
Enrollment
171 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2024 (Actual)
Primary completion
Jun 30, 2025 (Actual)
Completion
Jun 30, 2025 (Actual)
Last update posted
Jul 24, 2025

2024 – 2025

United States locations

U.S. sites
15
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
Lakeview Clinical Research Guntersville Alabama 35976 —
New Horizons Clinical Trials Chandler Arizona 85224 —
The Practice of Medicine INC. Eagle Rock California 90041 —
Finlay Medical Research Greenacres City Florida 33467 —
Finlay Medical Research Miami Florida 33126 —
Smith Medical Center Dunwoody Georgia 30338 —
Sonar Clinical Research Riverdale Georgia 30274 —
Leavitt Clinical Research Idaho Falls Idaho 83404 —
Research Integrity Owensboro Kentucky 42303 —
Revive Research Institute Dearborn Heights Michigan 48127 —
Trialfinity Clinical Research Center Hamilton New Jersey 08619 —
Albuquerque Clinical Trials Albuquerque New Mexico 87102 —
Prime Global Research The Bronx New York 10456 —
MultiSpecialty Clinical Research Johnson City Tennessee 37604 —
Trio Clinical Trials Houston Texas 77008 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06666426, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 24, 2025 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06666426 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →