Extraperitoneal Versus Transperitoneal Cesarean Section
Not Applicable
Completed
- Conditions
- Cesarean, Extraperitoneal
- Registration Number
- NCT02155569
- Lead Sponsor
- Ataturk University
- Brief Summary
The aim of the study is to compare post operative morbidity between extra peritoneal cesarian and trans peritoneal cesarean section.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
- elective cesarean (primary or repeated up to four)
Exclusion Criteria
- emergent cesarean
- macrosomia (fetal weight > 4500 g)
- history of major abdominal surgery
- suspected abnormal placentation
- placenta previa
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method post operative pain One hour before cesarean and 24 hour postoperatively Perceived pain scores will be measured by an visual analog scale.
- Secondary Outcome Measures
Name Time Method delivery time 2 minutes after delivery skin incision to delivery
operation time 5 minutes postoperatively skin incision to skin closure
hemoglobin differences one hour before cesarean, 48 hour postoperatively vomiting 48 hour thoracic and shoulder pain 48 hour Urogenital distress measured by Urogenital Distress Inventory One hour before cesarean and 24 hour postoperatively Oral intake 48 hour The percentage of patients who tolerates oral intake. Oral intake will be allowed 4-6 hour after cesarean for extraperitoneal group. For intraperitoneal group it will be allowed when patient passed gas.
nausea 48 hour need for extra analgesic 48 hour
Trial Locations
- Locations (1)
Ataturk University Hospital
🇹🇷Erzurum, Turkey
Ataturk University Hospital🇹🇷Erzurum, Turkey