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Comparison of the Effect of Meloxicam and Diclofenac and Their Side Effects on Pain After Inguinal Hernia Repair Operatio

Phase 3
Recruiting
Conditions
Inguinal hernia.
Inguinal hernia
Registration Number
IRCT20221126056613N7
Lead Sponsor
Oroumia University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
60
Inclusion Criteria

Diagnosed with inguinal hernia
American Society of Anesthesiology grade 1 physical status patients
Candidate for inguinal hernia repair surgery

Exclusion Criteria

Emergency surgery
The duration of the surgery more than one hour
A history of hepatic, renal or cardiovascular diseases
A history of upper GI bleeding
A history of taking analgesic medications in a 24 hours period before surgery

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain intensity. Timepoint: 0, 2, 4, and 6 hours after the surgery. Method of measurement: Visual Analogue Scale.;Biomarkers' serum levels. Timepoint: 6 hours after the surgery. Method of measurement: ELISA.;Nausea and vomiting. Timepoint: 0, 2, 4, and 6 hours after the surgery. Method of measurement: Likert scale for nausea and vomiting.
Secondary Outcome Measures
NameTimeMethod
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