Efficacy of a regional block in eye (Subtenons Block)for prevention of pain and changes in heart rate during squint surgery in children under general anaesthesia- A study
Phase 3
Completed
- Conditions
- Health Condition 1: null- squint surgery
- Registration Number
- CTRI/2012/12/003244
- Lead Sponsor
- All India Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
ASA 1 and 2 patients posted for elective squint surgery
Exclusion Criteria
a)Parent refusal
b)hypersensitivity to local anesthetic drugs
c)Any contraindication to subtenonâ??s block
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the efficacy of Subtenonâ??s Block in decreasing perioperative pain <br/ ><br>Timepoint: Intraoperative period, 0.5 hours, 1 hours, 2 hours, 4 hours, 6 hours, 12 hours and 24 hours
- Secondary Outcome Measures
Name Time Method To evaluate the efficacy of subtenons block in decreasing perioperative oculocardiac reflex and postoperative nausea and vomitingTimepoint: 0, 0.5, 1, 2, 6, 12, 24 hours