CTRI/2020/03/024088
Completed
未知
A prospective randomised double blinded study to compare efficacy of two different doses of dexmedetomidine for attenuation of pressor responses to laryngoscopy and endotracheal intubation under bispectral index- controlled general anaesthesia
JLN Medical College Ajmer0 sites120 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: Z768- Persons encountering health services in other specified circumstances
- Sponsor
- JLN Medical College Ajmer
- Enrollment
- 120
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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.
Outcomes
Primary Outcomes
Not specified
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