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 @ 10:38 PM
Ignite Modification Date:
2025-12-24 @ 10:38 PM
NCT ID:
NCT07129135
Eligibility Criteria:
Inclusion Criteria:
* Age 18-45 years
* Pregnant women diagnosed antenatally with placenta accreta spectrum (PAS).
* Pregnant women with history of previous one or more caesarian deliveries .
* Planned cesarean hysterectomy at ≥33 weeks of gestation.
* Singleton pregnancy.
* BMI \<35 kg/m²
* Suitable for standardized General anaesthesia
Exclusion Criteria:
* Previous bladder surgery or known urologic abnormalities.
* Bleeding tendency disorder
* Renal failure .
* Allergy to methylene blue dye.
* Emergency hysterectomy without time for protocol preparation.
* Conservative uterine- preservation management.
* Refusal or inability to provide informed written consent
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT07129135
Study Brief:
Protocol Section:
NCT07129135