RecruitingNot ApplicableNCT06944392
Evaluating Pumpkin Seed Oil Extract Supplementation on Bladder Function
Sponsor
Northwestern University
Enrollment
40 participants
Start Date
Apr 11, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
This is a pilot study to assess using validated outcome measures how ingesting pumpkin seed oil extract supports patient bladder function in a United States population.
Eligibility
Sex: FEMALEMin Age: 18 Years
Inclusion Criteria1
- All patients evaluated at Northwestern's IPHP who report bladder function consistent with overactive bladder (urinary urgency, with or without urinary frequency more than 8 times daily or nocturia, with or without urgency urinary incontinence) at their index visit, who are also willing to use a dietary supplement and not initiate additional behavioral, medication or procedural treatment for 12 weeks following pumpkin seed oil extract initiation.
Exclusion Criteria11
- Patients with any of the following will be excluded from the study:
- Use of other supplements that contain pumpkin seed oil
- ≥Stage 3 pelvic organ prolapse
- Urinary post-void residual ≥150cc
- Culture-proven urinary tract infection at time of study enrollment
- Recurrent urinary tract infection
- Neurogenic bladder
- Abdominal or pelvic malignancy
- Initiation of new overactive bladder medications or supplements during study period or in the 3 months immediately preceding study enrollment
- History of surgery in the past 12 months for pelvic organ prolapse, stress urinary incontinence, urgency urinary incontinence, or fecal or flatal incontinence
- Patient's primary language is not English
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Interventions
DIETARY_SUPPLEMENTPumpkin Seed Extract
This is the only intervention
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06944392
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