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 @ 8:03 PM
Ignite Modification Date:
2025-12-24 @ 8:03 PM
NCT ID:
NCT06111404
Eligibility Criteria:
Inclusion Criteria:
.Patients undergoing total laparoscopic hysterectomy for benign conditions (e.g., dysfunctional uterine bleeding, adenomyosis and uterine fibroids) with presence of previous cesarean section scar.
Exclusion Criteria:
* Patients with prior abdominal surgery other than CS.
* Patients treated with concomitant surgery, including laparoscopic pelvic lymphadenectomy, posterior vaginal colporrhaphy and tension-free vaginal or obturator tape procedures.
* Tubo-ovarian abscess.
* Endometriosis.
* Pelvic tuberculosis.
* Pelvic organ prolapses. .Patients with relative contraindication to general anesthesia (e.g. chronic liver cell failure.
.Patients with contraindication to laparoscopic surgery (e.g. severe cardio-pulmonary dysfunction).
* Bleeding tendency (e.g. anticoagulants, platelets disorders)
* Body mass index more than 35 Kg/m2
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT06111404
Study Brief:
Protocol Section:
NCT06111404