MedPath

A study to find out the extent of adhesions inside the abdominal cavity and the thickness of the uterine scar based on the characteristics of external skin scar in women with previous cesarean sectio

Not Applicable
Conditions
Health Condition 1: O998- Other specified diseases and conditions complicating pregnancy, childbirth and the puerperiumHealth Condition 2: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium
Registration Number
CTRI/2020/07/026713
Lead Sponsor
ot applicable
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

All Pregnant women with previous one caesarean section undergoing repeat caesarean at term

Pfannenstiel/ Midline vertical abdominal skin scar

Exclusion Criteria

Previous classical uterine incision

Previous laparotomy/laparoscopy/Myomectomy

Immunosuppressed individual (HIV, Long term

corticosteroid therapy)

Placenta previa, morbidly adherent placenta

Known endometriosis

Known Connective tissue disorders

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Dense intra-abdominal adhesionsTimepoint: 1 year
Secondary Outcome Measures
NameTimeMethod
Grade 3 or dehisced uterine scar <br/ ><br> <br/ ><br>Clinical factors associated with severity of intra-abdominal adhesions <br/ ><br>Timepoint: 1 year
© Copyright 2025. All Rights Reserved by MedPath