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Comparison of the effect of Acetaminophen, Pethidine and Ibuprofen on pain relief in patients with acute cholecystitis

Phase 2
Conditions
Acute cholecystitis.
Acute cholecystitis
Registration Number
IRCT201710059014N191
Lead Sponsor
Vice-chancellor for Research and Technology, Hamadan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
90
Inclusion Criteria

Age of 18 to 75 years;
Acute cholecystitis

Exclusion Criteria

Pregnancy;
using analgesic within pass 6 hours;
Addiction to narcotic or psychedelic;
Contraindication of Acetaminophen, Pethidine, or Ibuprofen;
Chronic renal failure

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Measuring severity of pain. Timepoint: before infusion and 30, 60, and 90 minutes after infusion. Method of measurement: using Visual Analog Scale (VAS).
Secondary Outcome Measures
NameTimeMethod
Assessing nausea and vomiting. Timepoint: before infusion and 30, 60, and 90 minutes after infusion. Method of measurement: by taking history.
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