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.
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