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to develop and use a patient information leaflet for patients undergoing Caserean section

Development, validation and evaluation of patient information leaflet for women undergoing Caesarean section - nil

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/04/065460
Enrollment
240
Registered
2024-04-09
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: 1- Obstetrics

Interventions

Intervention1: nil: nil

Sponsors

Dr B R Ambedkar State Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.American Society of Anesthesiologists (ASA) physical status I - II 2. Age – 18- 45 years females with full term gestation posted for elective Caesarean delivery.

Exclusion criteria

Exclusion criteria: 1.Unwilling to take part in the study

Design outcomes

Primary

MeasureTime frame
A change in the knowledge regarding the operationTimepoint: A Pre test will be given 1 day before scheduled Caesarean section and post test will be given after reading of PIL for minimum 20 minutes—

Secondary

MeasureTime frame
change in knowledge score in post caesarean patientsTimepoint: A Pre test will be given 1 day before scheduled Caesarean section and post test will be given after reading of PIL for minimum 20 minutes—

Countries

India

Contacts

Public ContactDr Ravneet Kaur Gill

Dr B R Ambedkar State Institute of Medical Sciences

drravneetkgill@gmail.com9501988361

Outcome results

None listed

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