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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
NameTimeMethod
post operative painOne hour before cesarean and 24 hour postoperatively

Perceived pain scores will be measured by an visual analog scale.

Secondary Outcome Measures
NameTimeMethod
delivery time2 minutes after delivery

skin incision to delivery

operation time5 minutes postoperatively

skin incision to skin closure

hemoglobin differencesone hour before cesarean, 48 hour postoperatively
vomiting48 hour
thoracic and shoulder pain48 hour
Urogenital distress measured by Urogenital Distress InventoryOne hour before cesarean and 24 hour postoperatively
Oral intake48 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.

nausea48 hour
need for extra analgesic48 hour

Trial Locations

Locations (1)

Ataturk University Hospital

🇹🇷

Erzurum, Turkey

Ataturk University Hospital
🇹🇷Erzurum, Turkey

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