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A Pilot Study to Evaluate PureWick for Nocturia

RecruitingNAAges 50 Years - anyFemaleNorthwell Health
NCT05090722 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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.

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📋 Eligibility rules (as published)
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.
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What it tests

  • PureWick System
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Where

2 sites
Weill Cornell Medicine
New York, United States
Multi-Specialty NHPP Syosset
Syosset, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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