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

Phase 3
Recruiting
Conditions
distal radius surgery.
Fracture of lower end of radius
S52.5
Registration Number
IRCT20230716058807N1
Lead Sponsor
Qazvin University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
90
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
The duration of surgery should be less than 45 minutes

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The amount and intensity of pain. Timepoint: 1, 3, 6 and 12 hours after the operation. Method of measurement: Using a ruler-like grading system (Visual Analog Scale) from 0 (no pain) to 10 (the most severe pain imaginable).
Secondary Outcome Measures
NameTimeMethod
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