NCT06666426 - This Study Will Collect Clinical and Patient Reported Experience Data From Participants Requiring Urine Output Management Overnight in the Home Setting. | Biotech Hunter

Enrollment

171

Participants

Timeline

Start Date

October 31, 2024

Primary Completion Date

June 30, 2025

Study Completion Date

June 30, 2025

Conditions

Adult Nocturnal EnuresisUrinary Incontinence (UI)

Interventions

DEVICE

PureWick System

The PureWick System consists of the PureWick Urine Collection System used with the PureWick Flex Female External Catheter, which are intended for non-invasive urine output management.

DEVICE

Hollister Female Urinary Pouch External Collection Device

The Hollister Female Urinary Pouch External Collection Device is intended to collect and contain urine for individuals with urinary incontinence.

Trial Locations (15)

10456

Prime Global Research, The Bronx

30274

Sonar Clinical Research, Riverdale

30338

Smith Medical Center, Dunwoody

33126

Finlay Medical Research, Miami

33467

Finlay Medical Research, Greenacres City

35976

Lakeview Clinical Research, Guntersville

37604

MultiSpecialty Clinical Research, Johnson City

42303

Research Integrity, Owensboro

48127

Revive Research Institute, Dearborn Heights

77008

Trio Clinical Trials, Houston

83404

Leavitt Clinical Research, Idaho Falls

85224

New Horizons Clinical Trials, Chandler

87102

Albuquerque Clinical Trials, Albuquerque

90041

The Practice of Medicine INC., Eagle Rock

08619

Trialfinity Clinical Research Center, Hamilton