Comparing efficacy of two different doses of DEXMEDETOMIDINE for supression of haemodynamic responses to laryngoscopy with BIS monitoring
Not Applicable
Completed
- Conditions
- Health Condition 1: Z768- Persons encountering health services in other specified circumstances
- Registration Number
- CTRI/2020/03/024088
- Lead Sponsor
- JLN Medical College Ajmer
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 120
Inclusion Criteria
Age group between 18 and 55 years.
Body weight 50 to 70 kg.
Patients belonging to ASA (American Society of Anaesthesiologists) physical status class-I and II.
Patients undergoing elective surgeries under general anaesthesia.
Exclusion Criteria
Patientâ??s refusal.
Uncooperative patients.
Any known hypersensitivity or contraindication to Dexmedetomidine.
History of convulsion, bleeding disorder, severe neurological deficit, thyroid disorder.
Patient with history of respiratory, cardiac, hepatic or renal disease (necessitating classification in ASA Class III or above).
Patients having a history of significant neurological, psychiatric, or neuromuscular disorders.
Anticipated difficult airway which requires >20seconds to intubate.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method