Evaluating Pumpkin Seed Oil Extract Supplementation on Bladder Function
Recruiting now · Not applicable
Conditions studied: Overactive Bladder (OAB)
In brief
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.
Key facts
- Study ID
- NCT06944392
- Run by
- Northwestern University
- People needed
- 40
- Starts
- 2025-04-11
- Expected to finish
- 2026-10-01
- Last updated by the study team
- 2026-04-23
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- 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.
You may not qualify if…
- 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
Where it is running
- Northwestern University — Chicago, Illinois, United States (enrolling)
Full record on ClinicalTrials.gov
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