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Clinical Trials/IRCT20230716058807N1
IRCT20230716058807N1
Recruiting
Phase 3

Comparison of postoperative analgesic effect of intravenous acetaminophen versus intravenous caffeine in distal radius surgery

Qazvin University of Medical Sciences0 sites90 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Qazvin University of Medical Sciences
Enrollment
90
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Willingness to participate in research with informed consent after giving necessary and sufficient explanations about the study
  • Age 20 to 60 years
  • Distal radius fracture
  • General anesthesia

Exclusion Criteria

  • Unwillingness to cooperate in the study
  • Cardiac patients with a history of HTN (heart rate over 100 during surgery/blood pressure over 140 mm Hg during surgery)
  • Occurrence of any problems and complications during the study
  • Pregnancy, breastfeeding and abortion less than 3 months
  • Allergy to acetaminophen/caffeine/morphine
  • Long\-term use of corticosteroids, antihistamines, narcotics and pain relievers
  • Vision and hearing problems and other disabilities
  • Chronic mental and physical illness (schizophrenia, diabetes, etc)
  • Liver patients (hepatitis, cirrhosis, etc.)
  • History of smoking, alcohol and drugs

Outcomes

Primary Outcomes

Not specified

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