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 @ 7:39 PM
Ignite Modification Date:
2025-12-24 @ 7:39 PM
NCT ID:
NCT03475303
Eligibility Criteria:
Inclusion Criteria:
* Age between 20 and 35 years
* Gestational age between 37-42 weeks
* BMI less than 30 kg/m2
* Have normal uncomplicated pregnancy
* Planned lower uterine segment Cesarean section
* Planned for primigravida or previous one or two Cesarean sections
* Planned to have spinal anesthesia
* Cesarean sections without intra-operative complications
* Accepting to participate in the study
Exclusion Criteria:
* • Emergency Cesarean section
* Gestational age less than 37 or more than 42 weeks
* BMI 30 kg/m2 or more.
* Multiple pregnancies
* Polyhydraminos
* Abnormal placenta
* Premature rupture of membranes
* Previous abdominal surgeries or uterine surgeries
* Not more than previous two Cesarean sections
* Anemia: Hemoglobin level less than 10 g/dl
* Cesarean section with intraoperative complications
* General anesthesia
* Fibroid uterus
* RH incompatibility ( as there maybe delay of availability of anti-d immunoglobulins)
* History of complicated pregnancy or delivery
* Medical disorders(hypertension, diabetes mellitus, cardiac, pulmonary, renal, hepatic, endocrine and autoimmune disorders).
* Women refusing participating in the study
* Women having any contraindications or refusing spinal anesthesia
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
35 Years
Study:
NCT03475303
Study Brief:
Protocol Section:
NCT03475303