Comparison of two techniques of pain relief using blocks for anorectal surgery in childre
Not Applicable
- Conditions
- Health Condition 1: Q429- Congenital absence, atresia and stenosis of large intestine, part unspecified
- Registration Number
- CTRI/2022/07/044214
- Lead Sponsor
- AIIMS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA-I or II
Undergoing anorectal surgeries
Exclusion Criteria
1 History of developmental delay or
intellectual deficit
2 parental refusal
3 history of allergy to local anaesthetics
4 rash or infection at local site
5 anatomical abnormalities
6 bleeding diathesis
7 coagulation disorders
8 history of renal
9 hepatic
10 neurological disorders
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Total post operative fentanyl requirement at 24 hoursTimepoint: Total post operative fentanyl requirement at 24 hours
- Secondary Outcome Measures
Name Time Method 1) Time to first analgesic requirement <br/ ><br>2) Intra operative fentanyl consumption <br/ ><br>3) Procedure time <br/ ><br>4) FLACC (recorded at postoperative 0.5,1,2,4,6,12,24 hours) <br/ ><br>5) adverse events during and after surgery <br/ ><br>6) intraoperative hemodynamic parameters ( HR, BP, Sp02) <br/ ><br>7) parental satisfaction regarding analgesia at the end of 24 hours following surgery <br/ ><br>8) quality of sleep on the first night following surgeryTimepoint: 0.5,1,2,4,6,12,24 hours