Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 10:55 PM
Ignite Modification Date:
2025-12-24 @ 10:55 PM
NCT ID:
NCT05358769
Eligibility Criteria:
Inclusion Criteria:
* stress UI or stress-dominant mixed UI (stress percent score more than urge percent score)
Exclusion Criteria:
* pregnancy or less than 12-month postpartum
* more than three vaginal deliveries or any prior operative delivery
* self-reported symptoms of pelvic organ prolapse or POP-Q stage \>2
* history of supervised PFMT within 12 months
* current medications for UI
* known zinc or copper deficiency or sensitivity
* connective tissue disease
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT05358769
Study Brief:
Protocol Section:
NCT05358769