ketamine and postoperative pain management

Not Applicable

• Conditions: Pregnancy and Childbirth; Surgery; Postoperative pain; Anaesthesia

• Registration Number: PACTR201404000807178
• Lead Sponsor: SELF

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2014-04-03
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 88

Inclusion Criteria

¿Informed and consenting patients
¿All Pregnant mothers scheduled for elective caesarean section under spinal anaesthesia
¿ASA 1 and ASA 2

Exclusion Criteria

¿Hypertensive disorders
¿Known clearly documented allergy to the study medication
¿History of psychiatric disorders(hallucinations)
¿Chronic opioid therapy
¿Sickle cell disease
¿Epilepsy
¿Emergency obstetric cases
¿Conversion to general anaesthesia

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The time to breakthrough pain experienced by the patients in the first 24 hours following caesarean section delivery;The time to breakthrough pain experienced by the patients in the first 24 hours following caesarean section delivery

Secondary Outcome Measures

Name	Time	Method
umeric pain score at break through pain Total analgesia requirement in the 24 hours