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 @ 3:56 AM
Ignite Modification Date:
2025-12-25 @ 3:56 AM
NCT ID:
NCT05471102
Eligibility Criteria:
Inclusion Criteria:
* Age: 20-40 years old.
* Pregnancy of singleton living fetus.
* Previous one or more cesarean sections.
* Gestational age: \> 36 weeks.
* Elective termination of pregnancy.
* Cases not requiring preoperative blood transfusion.
* Cases with focal area of placental adherence or invasion leaving sufficient healthy myometrial tissue for uterine repair and preservation.
* The following ultrasound markers such as "loss of clear retroplacental translucency", "myometrial thinning", "abnormal lacunae", "irregular bladder wall", "utero-vesical hypervascularity".
Exclusion Criteria:
* Multifetal pregnancy.
* More than four previous sections.
* Emergency termination of pregnancy due to antepartum hemorrhage, placental separation or rupture uterus.
* Intrauterine fetal death.
* Women with history of any medical disorder with pregnancy eg. Gestational diabetes and hypertension.
* Premature rupture of membranes.
* Cases misdiagnosed as placenta accreta by ultrasound preoperatively, and spontaneous full placental separation occurred intraoperative. "will be excluded before randomization"
* Cases with PAS with total invasion involving all placental lobules.
* Cases who will be managed by cesarean hysterectomy due to uncontrolled intraoperative bleeding.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
40 Years
Study:
NCT05471102
Study Brief:
Protocol Section:
NCT05471102