A quality improvement study for documentation in caesarean sections.

Not Applicable

• Conditions: Health Condition 1: O30-O48- Maternal care related to the fetus and amniotic cavity and possible delivery problems

• Registration Number: CTRI/2020/05/025079
• Lead Sponsor: Jawaharlal Institute of Postgraduate Medical Education and Research

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Primiparous women undergoing emergency caesarean section in JIPMER.

Exclusion Criteria

Primiparous women with malpresentations undergoing emergency caesarean section.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Completeness in documentation by the end of study quater (each quater is 3 months-total of 3 quaters is studied-9 months) after introduction of comprehensive proforma.Timepoint: From the time of surgery in JIPMER till the discharge around 4 to 6 days.

Secondary Outcome Measures

Name	Time	Method
ILTimepoint: NI