Pterygopalatine fossa block on postoperative pain relief in Adenotonsillectomy surgeries
Phase 3
- Conditions
- Health Condition 1: 8- Other Procedures
- Registration Number
- CTRI/2024/04/066145
- Lead Sponsor
- Bangalore Medical College and Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age 6 to 16 years
2.Patients belongs to ASA grade 1,2
3.Patients posted for elective adenotonsillectomy surgeries who are willing to give informed consent
Exclusion Criteria
1.Parents/caregivers refusal
2.Patients belongs to ASA grade 3,4
3.Hypersensitivity to Local anaesthetics
4.Any history of developmental delay, bleeding diathesis,mental retardation,upper or lower respiratory tract infections,skin lesions,wounds at the puncture site of block
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the total analgesic requirements in first 24 hrs postoperatively among the patients with and without Pterygopalatine fossa blockTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method To assess the time for first rescue analgesia, intraoperative haemodynamic changes and incidence of any complications among the patients with and without Pterygopalatine fossa blockTimepoint: 24 hours