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Comparison of Postoperative Pain in Two Groups of Children with Bone Fractures Receiving Pethidine and Paracetamol in Kerman Bahonar Hospital: A Clinical Trial Study

Comparison of Postoperative Pain in Two Groups of Children with Bone Fractures Receiving Pethidine and Paracetamol in Kerman Bahonar Hospital: A Clinical Trial Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20200921002
Enrollment
Unknown
Registered
2020-09-21
Start date
2019-09-24
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

6&#44

Interventions

the first group received pethidine (1mg per kg body weight) ,the second group received paracetamol (1gr)
Active Comparator Drug,Active Comparator Drug
pethidine,paracetamol

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 18 Years

Inclusion criteria

Inclusion criteria: Criteria for entering the study included parents’ consent and being aged under 18

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
Postoperative Pain 6,12, 24 hour after Visual Analog Scale—

Secondary

MeasureTime frame
- - -—

Countries

iran

Contacts

Public ContactAli Rokni

1Orthopedic Resident, Department of Orthopedic, Kerman University of Medical Sciences, Kerman, Iran

alirokni698795@gmail.com03432263719

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026