A clinical trial to study the efficacy of subtenons block for pain relief in children undergoing vitreoretinal surgery under general anaesthesia as compared to intravenous fentanyl alone
Phase 4
Completed
- Conditions
- Health Condition 1: null- Children undergoing vitreo- retinal surgeryHealth Condition 2: H33- Retinal detachments and breaks
- Registration Number
- CTRI/2009/091/000142
- Lead Sponsor
- one
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 200
Inclusion Criteria
ASA grade I and II children aged 5-15 years undergoing vitreo-retinal surgery will be studied after informed parental consent.
Exclusion Criteria
1.Parents of children unwilling to give consent.
2.Patients on peri-operative steroids.
3.Patients with any contra-indication to administering sub-tenon?s block i.e prior redness, inflammation in the eye.
4. any child undergoing only silicone oil removal surgery ( this is a minor posterior segment surgery.)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method