Comparison of two different drugs in attenuating the pressor response to laryngoscopy.
Phase 1
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/02/062801
- Lead Sponsor
- Dr V.Subikssha
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Elective surgery under general anaesthesia, ASA grade 1 and 2, Body weight 45-85 kg
Exclusion Criteria
Pregnant women, Anticipated difficult airway, nasotracheal intubation, allergy to general anaesthetic drugs, inability to give consent precluding to language barrier, patient refusal
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To observe changes in heart rate between the two study groupsTimepoint: Heart rate before induction, 1 min, 3 min, 5 min & 10 min after laryngoscopy
- Secondary Outcome Measures
Name Time Method To observe changes in systolic blood pressure, diastolic blood pressure & mean arterial pressureTimepoint: systolic blood pressure, diastolic blood pressure & mean arterial pressure before induction, 1min, 3 min, 5 min and 10 min after laryngoscopy