The clinical trial concerned with selection of the suturing methods for uterine wound relating to uterine tissue oxygen saturation in cesarean sectio
Not Applicable
Recruiting
- Conditions
- Pregnant women over 36 weeks of gestation who will undergo the first cesarean section
- Registration Number
- JPRN-UMIN000030063
- Lead Sponsor
- Department of Obstetrics and Gynecology, Hamamatsu University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
1. Pregnant women who will undergo cesarean section under general anesthesia 2. Pregnant women who had cesarean section 3. Multiple pregnancy 4. Patients having cardiovascular disturbances or a dyspneic condition 5. Uterine incision method other than lower transverse section 6. Transverse fetal lie
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the tissue oxygen saturation and total hemoglobin index of uterine wound between full thickness myometrial closure including the endometrial layer and myometrial closure excluding the endometrial layer
- Secondary Outcome Measures
Name Time Method To investigate the tissue oxygen saturation and total hemoglobin index compared between two groups as follows: 1. Closure at 1cm pitch versus closure at 2cm pitch in single-layer 2. Single-layer versus double-layer closure of lower uterine segment incision 3. The edge area of uterine wound versus the center of uterine wound 4. The lower side of uterine wound versus the upper side of uterine wound