Randomised study to see the effect of adding Transversus Abdominis plane block after Sub arachnoid block in reducing the dose of analgesic drugs postoperatively
Phase 3
- Conditions
- Health Condition 1: K409- Unilateral inguinal hernia, without obstruction or gangrene
- Registration Number
- CTRI/2023/09/057307
- Lead Sponsor
- Department of Anesthesiology and Crit Care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA I AND II FOR LOWER ABDOMEN SURGERY
Exclusion Criteria
history of drug intake (including opioids and benzodiazepines), sensitivity to prescribed analgesics, coagulopathy, Infection of the block injection site, receiving any drugs within 48 h of surgery (except for the study protocol).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method FLACC SCORINGTimepoint: three six twelve & twenty four hours
- Secondary Outcome Measures
Name Time Method total use of analgesic drug in 24 hours <br/ ><br>patient satisfaction scoreTimepoint: twelve & twenty four hours