Comparison of pediatric intravenous acetaminophen and acetaminophen suppository in hernia surgery
Phase 2
Recruiting
- Conditions
- Patients with inguinal hernia who are candidates for surgery.Inguinal hernia
- Registration Number
- IRCT20120911010811N2
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 159
Inclusion Criteria
Candidate for inguinal hernia repair surgery
Parents' consent based on children's participation in the study
Participants are children from 6 months to 3 years
Exclusion Criteria
History of bupivacaine allergy
Existence of local infection in the spine
Presence of pilonidal cyst
History of acetaminophen allergy
History of liver problems
History of heart disease
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The amount of analgesia. Timepoint: After inguinal hernia surgery in recovery. Method of measurement: Based on the behaivorial-FLACC criteria.
- Secondary Outcome Measures
Name Time Method