ongitudinal versus transverse extension of uterine incision during cesarean section: randomized controlled trial

Not Applicable

• Conditions: Pregnancy and Childbirth; Extension of uterine incision

• Registration Number: PACTR201711002795139
• Lead Sponsor: Airforce specialized Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-11-22
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 392

Inclusion Criteria

Age 18 or more.
Term pregnancy.
Elective previous one cesarean section

Exclusion Criteria

Any previous uterine scar other than CS or more than one previous CS
Multiple pregnancy
Malpresentation
Antepartum hemorrhage
Fetal macrosomia
Polyhydramnios
Any participation in another trial that interferes with this trial.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
nintended extension of the Uterine incision

Secondary Outcome Measures

Name	Time	Method
umber of additional stitches needed;Drop of hemoglobin level