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 @ 5:10 PM
Ignite Modification Date:
2025-12-24 @ 5:10 PM
NCT ID:
NCT00420550
Eligibility Criteria:
Inclusion Criteria:
* Established diagnosed IC patient
* Women at least 18 years of age
* Self reported pelvic pain
* Capable of giving informed consent
* Capable and willing to follow all study related procedures (e.g. keep voiding diary, pain diary, complete questionnaires, listening to CD, obtaining salivary samples).
* Participants must have a stable medication regimen.
* Neuromodulation (if present) must stay stable throughout the study.
Exclusion Criteria:
* Currently participating or have participated within the past 30 days in any clinical investigation involving or impacting urinary or renal function. Patients with neuromodulation devices are excluded for the first 3 months after insertion of the device.
* Use of this guided imagery CD within the past 30 days.
* Diagnosed depression
* Pregnancy or intending to become pregnant during the study
* Cannot independently comprehend and complete the questionnaires.
* The subject is deemed unsuitable for enrollment in this study by the investigators based on their history.
* Men are excluded
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT00420550
Study Brief:
Protocol Section:
NCT00420550