Comparative study between general anaesthesia without using drugs which reduces pain and plain general anaesthesia for stabilizing vitals in ear surgery:a prospective randomized clinical study
Phase 4
- Conditions
- Health Condition 1: H673- Otitis media in diseases classified elsewhere, bilateral
- Registration Number
- CTRI/2023/09/057341
- Lead Sponsor
- Baroda medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA grade 1 and 2
malampatti grade 1 and 2
patient diagnose with acute and chronic suppurative otitis media scheduled for mastoid surgery
patient able to give written and informed consent
patient able to understand Visual analogue scale regarding assessment of pain
Exclusion Criteria
Patient not willing for procedure
patient having uncontrolled diabetes,hypertention,liver and kidney disorder
pregnant patients
hypersensitivity to any local anaesthetic drug or drug used in this study
patient with significant history of drug or alcohol abuse,psychiatric illness
patient on beta blocker and calcium channel blockers
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary objective is to monitor hemodynamic stability intraoperativelyTimepoint: Baseline <br/ ><br>Before intubation <br/ ><br>During intubation <br/ ><br>After intubation <br/ ><br>Maintainance anaesthesia <br/ ><br>2 min <br/ ><br>5 min <br/ ><br>10 min <br/ ><br>20 min <br/ ><br>30 min <br/ ><br>60 min <br/ ><br>90 min <br/ ><br>120 min <br/ ><br>150 min <br/ ><br>180 min
- Secondary Outcome Measures
Name Time Method To observe <br/ ><br>post operative pain relief( first rescue analgesia) <br/ ><br>post operative any complication like nausea & vomitingTimepoint: Immediately post operative,30 min,1 hr,2 hr,4 hr,6 hr,8 hr,12 hr,16 hr,20 hr