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 @ 9:25 PM
Ignite Modification Date:
2025-12-24 @ 9:25 PM
NCT ID:
NCT00780832
Eligibility Criteria:
Inclusion Criteria:
1. Women with OAB symptoms including urgency, frequency (voids ≥8/day), and urge incontinence
2. Women who consume \> one cup (250ml) caffeinated beverage per day
3. Women who score $ 6 on the QUID Questionnaire for urgency symptoms
Exclusion Criteria:
1. Women currently receiving treatment for OAB symptoms
2. Women with narrow angle Glaucoma
3. Women taking anticholinergics or loop diuretics
4. Women with an untreated urinary tract infection. After resolution of the UTI, and if all other eligibility criteria are met, the woman can be a candidate for inclusion in the study.
5. Women with a diagnosis of painful bladder syndrome or other abnormal urinary tract lesions
6. Women scoring \>4 on the QUID Questionnaire for stress symptoms
7. Women with de novo symptoms following surgery
8. Women with major pelvic prolapse
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT00780832
Study Brief:
Protocol Section:
NCT00780832