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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 Jul 21, 2026, 6:51 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)

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

Interventions

  • PureWick System Device
  • Hollister Female Urinary Pouch External Collection Device Device

Device

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 30, 2024
Primary completion
Jun 29, 2025
Completion
Jun 29, 2025
Last update posted
Jul 23, 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 23, 2025 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06666426 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →