Expansion of the low transverse uterine incision at cesarean sectio
Not Applicable
- Conditions
- Cesarean.Single delivery by caesarean section
- Registration Number
- IRCT2017051533989N1
- Lead Sponsor
- Zahedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 288
Inclusion Criteria
All women with singleton pregnancy, gestational age between 37 to 42 weeks who are candidate for elective or emergency cesarean section and give informed constsnt for our research.
Exclusion criteria: Unknown gestational age, preterm or postterm pregnancy, placenta previa, abruptio placenta, severe hemorrhage before cesarean section,BMI greater than 30, polyhydramnios, connective tissue disorders, estimated fetal weight greater than 4000 gr, uterine atony during or after cesarean section
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method nwanted extension of uterine incision to cervix, vagina, upper segment of uterus with need to additional sutures. Timepoint: Just after intervention. Method of measurement: Yes or no with evaluator assessment.;Need to additional sutures for control of bleeding of uterine incision after repair of that. Timepoint: Just after intervention. Method of measurement: yes or no with evaluator assessment.;Need to blood transfusion. Timepoint: After intervention. Method of measurement: Yes or no with evaluator assessment.;More than 10% Hb decrease after cesarean section. Timepoint: After intervention. Method of measurement: Yes or no with medical record assessment.;Assessment of intraoperation blood loss. Timepoint: Just after intervention. Method of measurement: Assessment by evaluator / mili liter.
- Secondary Outcome Measures
Name Time Method