MedTrace Logo

Delayed Primary Closure of Skin in Emergency Caesarean Section

NCT04587960 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2021-10-01

No results posted yet for this study

Summary

Pregnant mothers requiring emergency cs with history of ruptured membranes would be allocated randomly into two groups in an aim to study the comparative outcome of different methods of skin closure namely primary and delayed primary closure on the incidence of wound infections requiring secondary closures and to detect the associated risk factors increasing chance of surgical site infections.

Conditions

  • Cesarean Wound Disruption
  • Cesarean Section; Infection

Interventions

PROCEDURE

Delayed primary closure of skin incision in Caesarean section in experimental group

Delayed closure of skin wound of emergency Caesarean section following wound dressing for 2-3 days in experimental group

PROCEDURE

Primary closure of skin incision in Caesarean section in active comparator group

Primary closure of skin wound (incisional) at the time of emergency Caesarean section in active comparator group

Sponsors & Collaborators

  • Dr.Jhuma Biswas

    lead OTHER_GOV

Principal Investigators

  • Jhuma Biswas, MBBS, MS · Dept. of Obstetrics and Gynecology, Calcutta National Medical College and Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-01
Primary Completion
2021-06-15
Completion
2021-06-15

Countries

  • India

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04587960 on ClinicalTrials.gov