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 @ 11:32 PM
Ignite Modification Date:
2025-12-24 @ 11:32 PM
NCT ID:
NCT07271056
Eligibility Criteria:
Inclusion Criteria:
* ≥1 previous cesarean section
* Post cesarean section uterine niche confirmed by saline infusion sonohysterography (niche depth ≥2 mm)
* Residual myometrial thickness ≥2.5 mm as confirmed by saline infusion sonohysterography
* Regular cycles
* Abnormal uterine bleeding for ≥3 consecutive cycles
* Post menstrual spotting or brownish discharge ≥2 days
* Total monthly bleeding duration \>7 days
Exclusion Criteria:
* Irregular cycles
* Amenorrhea
* Abnormal cervical cytology
* Acute or chronic cervicitis
* Pelvic inflammatory disease
* Endometrial polyps
* Uterine fibroids
* Contraindications to spinal or general anesthesia
* Refusal to participate
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT07271056
Study Brief:
Protocol Section:
NCT07271056