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Clinical Trials/IRCT20210511051268N1
IRCT20210511051268N1
Not yet recruiting
Phase 3

The effect of premedication with oral acetaminophen on the prevention of localized pain from intravenous injection of propofol as induction agent in patients under general anesthesia

Tehran University of Medical Sciences0 sites150 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
ocal Pain due to intravenous injection of propofol.
Sponsor
Tehran University of Medical Sciences
Enrollment
150
Status
Not yet recruiting
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
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • All patients for whom propofol is used as an induction of anesthesia

Exclusion Criteria

  • Weight less than 50 kg
  • Chronic pain in any area of ??the body
  • High blood pressure
  • Cardiovascular disease
  • Cerebrovascular disease
  • Difficulty communicating (even if there is a marked drop in level of consciousness with the initial injection dose)
  • Abnormal liver function test results (AST and ALT more than twice normal)
  • Kidney failure or creatinine clearance greater than 1\.2
  • Allergy to acetaminophen
  • Allergy to propofol

Outcomes

Primary Outcomes

Not specified

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