A Pilot Study to Evaluate PureWick for Nocturia
Northwell Health · with Becton, Dickinson and Company · NCT05090722
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 50+ · Women only
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 40
- US sites recruiting
- 1
- Study start
- December 16, 2021
- Record last updated
- June 15, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: PureWick System
Conditions: Nocturia
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
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.
Recruiting US locations
Multi-Specialty NHPP Syosset
Syosset, NY 11791
Site contact: Bilal Chughtai, MD · 516-628-5910 · Bchughtai@northwell.edu
Study contacts (from the official record)
- Bilal Chughtai, MD · 516-628-5910 · bchughtai@northwell.edu
- Jennifer Polo, CCRC · 516-628-5910 · Jpolo1@northwell.edu
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