A randomized control study to evaluate the of effect of infiltration of a long acting local anesthetic like bupivacaine, on post operative pain outcome in patients undergoing tonsillectomy .
Phase 1
- Conditions
- Health Condition 1: J039- Acute tonsillitis, unspecifiedHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2023/10/058194
- Lead Sponsor
- Shubham bhatnagar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Children between 5-14 years of age scheduled to undergo tonsillectomy for chronic tonsillitis .
Exclusion Criteria
1.Patients whose parents/guardians are not giving consent for participating in the study.
2. Patients unfit for surgery .
3. Patients having hypersenstivity to bupivacaine .
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method pain outcomeTimepoint: post operative pain outcome on post operative day 0 , 1 , 3 and 5
- Secondary Outcome Measures
Name Time Method 1)Tonsillar fossa healing score <br/ ><br>2)Mean time of return to normal diet (in days) , Post op intake(duration, input) <br/ ><br>3)Post tonsillectomy requirement of analgesic(I.V Paracetamol) <br/ ><br>Timepoint: 18 months