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Clinical Trials/CTRI/2015/01/005424
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
nil

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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