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Clinical Trials/CTRI/2019/09/021299
CTRI/2019/09/021299CompletedNot Applicable

An Observational study comparing the efficacy of low dose ketamine and paracetamol pretreatment in alleviating pain due to propofol injection.

DRSHAJI MATHEW1 site in 1 country300 target enrollmentStarted: September 25, 2019Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
300
Locations
1
Primary Endpoint
to observe for pain reduction immediately after administration of 1/3rd dose of propofol then 1 min and 2 min

Study Overview

Brief Summary

Propofol short acting intravenous anaesthetic agent is extensively used because of its smooth induction and recovery .Its a agent of choice in day care anaesthesia ,for sedation in ICU,as maintenance agent in anaesthesia.However pain due to this is major drawback.Various strategies have been practiced to reduce pain  like choosing a larger vein,cooling propofol,dilution of propofol,increasing speed of injection.

Ketamine and paracetamol are good analgesic properties so in this study comparing between two which provides better pain relief.

Study Design

Study Type
Observational

Eligibility Criteria

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

Inclusion Criteria

  • American Society of Anesthesiologists physical status (ASAPS) I and II patients undergoing elective surgeries under general anaesthesia.

Exclusion Criteria

  • Suspected allergy to propofol,ASAPS 3 and 4,patient refusal,emergency surgeries.

Outcomes

Primary Outcomes

to observe for pain reduction immediately after administration of 1/3rd dose of propofol then 1 min and 2 min

Time Frame: to observe for pain reduction immediately after administration of 1/3rd dose of propofol then 1 min and 2 min

Secondary Outcomes

  • to observe for hemodynamic changes if any before administering drug ,after intubation ,5 mins after intubation ,10 mins after intubation(0,5,10 mins)

Investigators

Sponsor
DRSHAJI MATHEW
Sponsor Class
Private medical college

Study Sites (1)

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