Comparison of Postoperative Pain in Two Groups of Children with Bone Fractures Receiving Pethidine and Paracetamol in Kerman Bahonar Hospital: A Clinical Trial Study
Not Applicable
Completed
- Conditions
- 6ᄼ,and 24 hours after being treated,both groups'pain intensity was assessed based on the VAS scaleChildren,Pethidine,Paracetamol,Clinical Trial Study
- Registration Number
- TCTR20200921002
- Lead Sponsor
- Kerman University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 25
Inclusion Criteria
Criteria for entering the study included parents’ consent and being aged under 18
Exclusion Criteria
paracetamol restrictions use due to liver issues and allergies, and pethidine restrictions due to respiratory issues, allergy, etc., and opioid abuse such as cases of children addicted to opioids.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative Pain 6,12, 24 hour after Visual Analog Scale
- Secondary Outcome Measures
Name Time Method - - -