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

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DIETARY_SUPPLEMENTPumpkin Seed Extract

This is the only intervention


Locations(1)

Northwestern University

Chicago, Illinois, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06944392


Related Trials