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Comparison of two techniques of cesarean section (extra peritoneal cesarean section vs trans peritoneal cesarean section)

Comparison of Extra-Peritoneal Cesarean Section with Conventional Trans-Peritoneal Cesarean Section: An Open Label Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/03/032242
Enrollment
68
Registered
2021-03-23
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O82- Encounter for cesarean delivery without indication

Interventions

Intervention1: Extra peritoneal cesarean section: Patients will be recruited from Obstetrics and Gynecology OPD or emergency, AIIMS Rishikesh after screening for eligibility criteria. Once patients ar

Sponsors

AIIMS RISHIKESH
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients who are planned for cesarean section (both emergency and elective sections). Patient with previous LSCS will also be included in the study. Patients who are willing to provide written informed consent.

Exclusion criteria

Exclusion criteria: Acute fetal distress Abnormal placentation (placenta previa, adherent placenta) Abruptio placentae Cord prolapse Coagulation defects An adnexal mass or fibroid at lower uterine segment.

Design outcomes

Primary

MeasureTime frame
fetus delivery time among extra-peritoneal and Trans- peritoneal ap-proaches of cesarean Section.Timepoint: 1 year 6 months

Secondary

MeasureTime frame
Pain score as measured by Visual Analog Scale on day 0 & day 1 Return of bowel function as measured by time of appearance of bowel sounds on auscultation and by time of passage of flatus. Intra operative complications will be documented, if any. Total operation time as measured by time of skin incision to skin closure. APGAR score of fetuses at 1 min and 5 min The incidence of post-operative nausea/ vomiting/ others will be documented. Duration of hospital stay. Timepoint: 1 year 6 months

Countries

India

Contacts

Public ContactDR KAVITA KHOIWAL

AIIMS RISHIKESH

kavita.kh27@gmail.com9013436908

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026