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Study identifier: NCT05090722 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Pilot Study to Evaluate PureWick for Nocturia

Condition: Nocturia  ·  Sponsor: Northwell Health

PhaseNA
Planned participants40
Who can joinFemale, 50 Years to no upper limit
Healthy volunteersYes

About this 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.

This description comes directly from the study's public registry record.

Talk to the study team

Bilal Chughtai, MD  ·  516-628-5910  ·  bchughtai@northwell.edu

Jennifer Polo, CCRC  ·  516-628-5910  ·  Jpolo1@northwell.edu

Always discuss trial participation with your own doctor first.

Locations (2)

Weill Cornell MedicineNew York, New York, United StatesCompleted
Multi-Specialty NHPP SyossetSyosset, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05090722