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:
2025-12-25 @ 2:23 AM
Ignite Modification Date:
2025-12-25 @ 2:23 AM
NCT ID:
NCT05417334
Eligibility Criteria:
Inclusion Criteria:
* 4-9 postpartum
* de novo dyspareunia after delivery
* obstetric injury
* Grant informed consent
Exclusion Criteria:
* radiofrequency contraindications (pacemaker, active infection or pregnancy)
* cesarean section
* dyspareunia previous to labour
* previous vulvo-vaginal pathology
* patients with postpartum depression
* patients with a pelvic region oncological history
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT05417334
Study Brief:
Protocol Section:
NCT05417334