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 @ 10:14 PM
Ignite Modification Date:
2025-12-24 @ 10:14 PM
NCT ID:
NCT01123135
Eligibility Criteria:
Inclusion Criteria:
* English speaking
* Postmenopausal women (No menses for a minimum period of 1 year)
* Urodynamic stress urinary incontinence
Exclusion Criteria:
* History of breast or uterine cancer
* History of venous thrombolic event
* Hormone replacement therapy within 3 months of study
* Sensitivity or allergy to premarin cream
* Current use of any medications for urge or stress incontinence
* Prior surgery for stress incontinence
* Overactive bladder or Detrussor instability
* Active vaginal/ bladder infection (patients will be treated and have a negative test for cure in order to be enrolled in the study)
* History of pelvic or vaginal radiation therapy
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT01123135
Study Brief:
Protocol Section:
NCT01123135