CTRI/2015/01/005424
Completed
未知
Prevention of pain due to propofol injection: A comparative study of lignocaine, dexmedetomidine and placebo.
nil0 sites90 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- ASA I & II undergoing surgery under general anaesthesia
- Sponsor
- nil
- Enrollment
- 90
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Written informed consent.
- •Patients of either sex.
- •Aged between 17 \-70 years
- •Belonging to ASA GRADE 1 and 2( Based on the physical status,the patients are classified into categories by American Society of Anaesthesiologists)
- •Requiring standard General Anaesthesia (G.A)
Exclusion Criteria
- •Concomitant analgesic or sedative medication, patients requiring rapid sequence induction, anticipated difficulty venous access, difficulty in communication
- •Known sensitivity to lignocaine or dexmedetomidine
- •Conditions where use of lignocaine and dexmedetomidine may be harmful
- •Presence of infection on the dorsum of hand
Outcomes
Primary Outcomes
Not specified
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Not Applicable
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