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Clinical Trials/CTRI/2018/03/012482
CTRI/2018/03/012482Not yet recruitingUnknown

Evaluation of pretreatment with Lignocaine,Dexmedetomidine or Ketamine in providing relieffrom Propofol injection pain and withdrawalmovements during induction of Anaesthesia

Vardhaman Mahavir Medical College and Safdarjung Hospital1 site in 1 country135 target enrollmentStarted: March 15, 2018Last updated:

Trial Snapshot

Phase
Unknown
Status
Not yet recruiting
Sponsor
Enrollment
135
Locations
1
Primary Endpoint
during induction of anaesthesia, using lignocaine, dexmedetomidine or ketamine as

Study Overview

Brief Summary

1.To study the degree of alleviation of pain and withdrawal movements, with propofol injection during induction of anaesthesia, using lignocaine, dexmedetomidine or ketamine as pretreatment.

2.To study the variations in haemodynamic parameters.

HYPOTHESIS : Pretreatment with dexmedetomidine would be comparable to ketamine and lignocaine in providing relief from pain and withdrawal movements associated with propofol injection during induction of anaesthesia.

Study Design

Study Type
Interventional
Allocation
Computer generated randomization
Masking
Participant Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 65.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • ASA grade I & II
  • BMI less than or equal to 30 kg/m2
  • undergoing elective surgical procedures under general anaesthesia with endotracheal intubation.

Exclusion Criteria

  • History of pulmonary, renal, hepatic, endocrine, neurological or cardiovascular disease(including hypertension, those on beta blockers or digitalis),patients on any sedatives, anxiolytics or analgesics, history of drug abuse and psychiatric illness, known hypersensitivity to the study drugs.
  • Pregnant and nursing females and emergency surgical procedures.
  • Subjects with anticipated difficulty in venous access.

Outcomes

Primary Outcomes

during induction of anaesthesia, using lignocaine, dexmedetomidine or ketamine as

Time Frame: At the time of induction.

To study the degree of alleviation of pain and withdrawal movements, with propofol injection

Time Frame: At the time of induction.

pretreatment.

Time Frame: At the time of induction.

Secondary Outcomes

  • To study the variations in haemodynamic parameters.(At the time of induction, preintubation , intubation and post intubation.)

Investigators

Sponsor
Vardhaman Mahavir Medical College and Safdarjung Hospital
Sponsor Class
Government medical college

Study Sites (1)

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