Effect of remifentanyl on intubation response in hyper tensive patients.
Not Applicable
- Conditions
- Health Condition 1: - Health Condition 2: O- Medical and SurgicalHealth Condition 3: O- Medical and Surgical
- Registration Number
- CTRI/2024/08/072528
- Lead Sponsor
- Dr Annu Choudhary
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with Primary Hypertension Grade 1 & 2, ASA II, posted for elective surgery under general anaesthesia
Exclusion Criteria
•Patient’s refusal to participate
•Uncompensated cardiovascular, pulmonary, neurological, hepato-renal, endocrine disorders
• Allergy to study drugs
• Any substance abuse disorders.
•Viral marker status positive
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method change in BIS values on laryngoscopyTimepoint: immediately after intubation (Ti)
- Secondary Outcome Measures
Name Time Method Comparison of time to achieve BIS 50 in between two groups <br/ ><br> 2. Comparison of total propofol consumption for induction in between the two groups <br/ ><br> 3. Incidence of any adverse effects in two groups <br/ ><br> 4. Comparison of change in vital parameter ( HR, MAP,SpO2, RR) <br/ ><br>Timepoint: Baseline <br/ ><br>(0min) 1 min2 min3 min4 min5 min6 min7 min8 min9 min10 min <br/ ><br>Before inductionAfter inductionBefore laryngoscopyAfter intubation (Ti)5 min10 mins30 min60 min <br/ ><br>end of surgery <br/ ><br>