A study to compare the effect of Dexmedetomidine and Lignocaine in preventing Etomidate-induced Myoclonus
Not Applicable
- Conditions
- Health Condition 1: 4- Measurement and Monitoring
- Registration Number
- CTRI/2021/06/034499
- Lead Sponsor
- Shammy
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA grade I and II
Patients willing to participate
Exclusion Criteria
1. Bradycardia
2. Upper respiratory tract infection 2 weeks before surgery
3. History of allergy to study drugs (Dexmedetomidine, Lignocaine, Etomidate)
4. Diabetes Mellitus, Hypertension, Cardiovascular, Respiratory and Neurologic disease
5. Adrenocortical dysfunction
6. Morbid obesity
7. Emergency surgery patients
8. Received sedatives, analgesics or opioids within 24 hours prior to surgery
9. Communication problems
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method