Comparison of incidence of post-operative vomiting after squint surgery in childre
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/03/031859
- Lead Sponsor
- arayana Nethralaya
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
70 consecutive ASA I-II children aged 1-12 years undergoing strabismus surgery under general anaesthesia will be recruited after obtaining written parental consent.
Exclusion Criteria
Patients with a known allergy to propofol, those with a known difficult airway and those with a severe neurological disorder will be excluded from the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.The primary outcome is to compare the incidence of postoperative vomiting in children undergoing strabismus surgery under intravenous versus balanced anaesthesiaTimepoint: 0-2 hour, 2-6 hour and 6-24 hour
- Secondary Outcome Measures
Name Time Method 2.The secondary outcome is to compare the incidence of emergence agitation in the two groupsTimepoint: 0-2 hour