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Clinical Trials/TCTR20210802005
TCTR20210802005
Completed
Phase 1

Comparison of postoperative pain between pethidine and paracetamol recipients with tibial fractures undergoing nailing surgery in Bahonar Hospital

Kerman University of Medical Sciences0 sites96 target enrollmentAugust 2, 2021

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
compare the postoperative pain intensity between pethidine and paracetamol (Aptol) recipients with tibial fractures who underwent nailing surgery.
Sponsor
Kerman University of Medical Sciences
Enrollment
96
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 2, 2021
End Date
August 14, 2019
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Patients with tibial fracture over 18 years of age and under 50 years of age who were candidates for tibial nail surgery.
  • 2\. Patients with tibial fracture who were classified into 42a, 42b and 42c groups according to AO classification.

Exclusion Criteria

  • 1\. Any contraindications to paracetamol include liver disease and allergies
  • 2\. Any contraindications to the use of pethidine, including respiratory and drug\-sensitive diseases.
  • 3\. If it is not possible to use the tibial nailing (such as fractures at the end and beginning of the tibia bone that cannot be nailed, or the tibial canal diameter is less than 8mm and thus, the nail cannot pass, or the tibia physe is open where nailing is forbidden).
  • 4\. Lack of consent to participate in the research project
  • 5\. Age over 50 years
  • 6\. Opium consumption
  • 7\. History of substance abuse (addicts)
  • 8\. People who received analgesics for any reason.

Outcomes

Primary Outcomes

Not specified

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