MedPath

A study done to assess the perception of labour pain relief management among mothers who undergo delivery at our institute.

Not Applicable
Conditions
Health Condition 1: 8- Other Procedures
Registration Number
CTRI/2023/08/056381
Lead Sponsor
Shilpa Dan D
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

All women who had delivered in our institution via normal vaginal delivery, instrumental delivery, emergency Caesarean section

Exclusion Criteria

Women who are not willing to participate in the study

Women who have undergone elective Caesarean section

Women in the age group of less than 19 years or more than 40 years

Women who are unable to read and write on their own

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess the perception of postnatal women on labour pain relief methodsTimepoint: 24hrs to 48hrs
Secondary Outcome Measures
NameTimeMethod
Correlation between socio-demographic factors & the perception on labour pain relief methods & labour epidural will be assessed. The variables in the questionnaire include age, level of education of the women, income, occupation, previous experience on labour, previous knowledge of epidural analgesia. <br/ ><br>To find out the various reasons for the refusal of labour epidural among our postnatal patients. <br/ ><br>Timepoint: 24hrs to 48hrs
© Copyright 2025. All Rights Reserved by MedPath