comparison of two simple tools for relatability to acute postoperative pain after caeserean delivery
Not Applicable
Completed
- Conditions
- Health Condition 1: 1- Obstetrics
- Registration Number
- CTRI/2019/03/018076
- Lead Sponsor
- Divya Gupta
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 150
Inclusion Criteria
1.Healthy parturient
2.Uncomplicated singleton pregnancy under spinal anaesthesia
Exclusion Criteria
1.Category 1 Emergency caesarean section
2.Documented psychiatric illness
3.History of chronic alcohol, opioid or drug abuse
4.Failure of neuraxial anaesthesia
5.Allergy to study medications
•Unwilling to participate
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evoked pain on VAS scale(1-10)Timepoint: 24 hours postoperative
- Secondary Outcome Measures
Name Time Method Pain at rest <br/ ><br>Analgesics consumption in 24 hours <br/ ><br>â?¢Patient satisfaction. <br/ ><br>Timepoint: at 24 hours