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 @ 7:35 PM
Ignite Modification Date:
2025-12-24 @ 7:35 PM
NCT ID:
NCT05806203
Eligibility Criteria:
Inclusion Criteria:
* Primary diagnosis of dyspareunia (pain with intercourse and/or vaginal penetration)
* Cisgender female or have natal vaginal tissu
* Has not started hormonal therapy within the past 2 weeks
* Has not received pelvic floor physical therapy within the past 2 weeks
* Is able to electronically access informed consent and outcomes measures forms
Exclusion Criteria:
* Have a diagnosis of lichen sclerosis
* Have an active infection (e.g. herpes)
* Are earlier than 12 weeks post-surgery
* Are earlier than 6 weeks postpartum
* Have a history of gynecological cancer
* Have a history of pelvic radiation
* Are actively undergoing cancer treatments
* Are currently pregnant
* Currently using lidocaine or cortisone
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
21 Years
Maximum Age:
65 Years
Study:
NCT05806203
Study Brief:
Protocol Section:
NCT05806203