A Pilot Study to Evaluate PureWick for Nocturia

Recruiting now · Not applicable

Conditions studied: Nocturia

In brief

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.

Key facts

Study ID

NCT05090722

Run by

Northwell Health

People needed

40

Starts

2021-12-16

Expected to finish

2027-10-01

Last updated by the study team

2026-06-15

Who can join

Age: 50 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

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

You may not qualify if…

• 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.

Where it is running

• Multi-Specialty NHPP Syosset — Syosset, New York, United States (enrolling)
• Weill Cornell Medicine — New York, New York, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.