Home › Nocturia › NCT05090722

A Pilot Study to Evaluate PureWick for Nocturia

Who can join

Ages 50 and older · Women · Healthy volunteers welcome

Inclusion Criteria:

* Women aged 50 years or older.
* Experiences 2 or more voids per night as assessed on a 3-day bladder diary.

Exclusion Criteria:

* Compromised skin integrity in the perineal area (e.g., ulcers, open wounds, etc.).
* Neurological impairment or psychiatric disorder preventing proper understanding of consent.
* Unable to operate the PureWick system.
* Unable to complete required questionnaires and diaries.
* Investigator deems subject as unsuitable for enrollment.

About the study

This is a single-center prospective pilot study of PureWick used as a management for nocturia and reduction of nighttime falls associated with going to the bathroom. Subjects are followed up to 3 months after the intervention. As a pilot study, it is expected that a 3-month follow-up will adequately capture urinary and sleep outcomes data and any adverse events related or unrelated to the study device.

What is being tested

• PureWick System (device)

Sponsor: Northwell Health · Participants: 40 · Started: Dec 16, 2021

Contact the study team

• Bilal Chughtai, MD · Phone: 516-628-5910
• Jennifer Polo, CCRC · Phone: 516-628-5910

Official record on ClinicalTrials.gov — NCT05090722

Locations in the U.S.

Conditions

• Nocturia

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.