to study the effectiveness of propofol administered at the end of the surgery for prevention of emergence agitation in children undergoing adenotonsillectomy
Not Applicable
- Conditions
- Health Condition 1: J353- Hypertrophy of tonsils with hypertrophy of adenoids
- Registration Number
- CTRI/2024/08/071825
- Lead Sponsor
- Department of anaesthesia Sawai Man Singh Medical College JLN marg Jaipur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. All elective ASA I & II paediatric patients of either sex, age between 3-10 years
undergoing adenotonsillectomy under general anaesthesia.
2. Patient’s parents willing to give consent.
Exclusion Criteria
1. Patients part of any other study.
2. Non co-operative patient.
3. Patient with known allergy to propofol.
4. Patient with known psychiatric disorder.
5. Patients having upper respiratory tract infection.
6. Patient requiring intra operative propofol for any indication
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method