A Pilot Study to Evaluate PureWick for Nocturia

Recruiting N/A Interventional Study
Nocturia
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
50 and older
Sex
Female
Study type
Interventional
Purpose
Treatment
Participants needed
40 (estimated)
Sponsor
Northwell Health · Other
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About This Trial
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 de…
Trial Locations
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Eligibility 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 p…
Contacts

Bilal Chughtai, MD

516-628-5910

bchughtai@northwell.edu

CONTACT

Jennifer Polo, CCRC

516-628-5910

Jpolo1@northwell.edu

CONTACT