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 @ 9:43 PM
Ignite Modification Date:
2025-12-24 @ 9:43 PM
NCT ID:
NCT06615232
Eligibility Criteria:
Inclusion Criteria:
* Reports vaginal washing beyond the introitus in the past week
* Female, aged 18-50
* Presence of a cervix
* Informed consent obtained and form signed
* HIV-seronegative
* Non-pregnant (urine β-hCG negative)
* Willing to abstain from sex for 14 days after biopsy
* Post-menarche and pre-menopause
Exclusion Criteria:
* \<3 months postpartum or current breastfeeding
* Current menstruation (can enroll after menses)
* History of bleeding disorder
* Visible cervical abnormality requiring evaluation
* Medical contraindication to study protocol
* Visible cervicovaginal ulcers or lesions
* Positive test for gonorrhea, chlamydia, trichomonas, or wet preparation and examination findings indicating vulvovaginal candidiasis
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT06615232
Study Brief:
Protocol Section:
NCT06615232