Comparison between Clonidine and Lignocaine in response to laryngoscopy and endotracheal intubatio
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/10/037063
- Lead Sponsor
- Dr Shahbaz Haroon
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Age between 18-60 yr of either sex.
2. ASA grade I and grade II.
3. Patients posted for elective surgeries under general anesthesia requiring intubation.
4. Hemodynamically stable patients having all routine investigations within normal limits.
5. Patients who give written informed consent and are willing to be part of the study.
Exclusion Criteria
1. Patients refusal.
2. Patients with ASA physical status III and more.
3. Patients with any pre-existing cardiovascular disease.
4. Patients with h/o allergy to test drugs.
5. Patients posted for emergency surgeries.
6. Patients with difficult airway.
7. Patients with neurological disorders and muscle diseases.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To observe the attenuation of pressor responses to laryngoscopy and endotracheal intubation with intravenous clonidineTimepoint: PRE INTUBATION, SCOPY 0 MINS, EVERY 5 MINUTES, UPTO 2 HOURS INTRA-OP, POST OP VAS, SEDATIO
- Secondary Outcome Measures
Name Time Method To study the side effects of Clonidine and Lignocaine, if any and Ramsay sedation scaleTimepoint: Ramsay sedation scale: immediately, 1 hour, 6 hour and 12 hour after surgery