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Clinical Trials/IRCT20220727055567N1
IRCT20220727055567N1
Recruiting
Phase 2

Comparing effects of local injection of bupivacaine with and without fentanyl at the site of surgery in open reduction mandibular surgeries on acute pain intensity and opioid requirement: a randomized clinical trial

Tabriz University of Medical Sciences0 sites44 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Fracture of mandible.
Sponsor
Tabriz University of Medical Sciences
Enrollment
44
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Candidate patients for open mandibular surgery
  • Age above 18 years
  • Duration of surgery less than 4 hours
  • Candidate patients for general anesthesia
  • Consent to jaw fixation

Exclusion Criteria

  • Unwillingness to cooperate in the study
  • The occurrence of any complications that prevent participation in the study
  • Hypersensitivity to fentanyl, bupivacaine, and other drugs
  • The patient's lack of satisfaction with intermaxillary fixation after the operation
  • Existence of underlying disease and confounding factor such as: hemorrhagic diseases and coagulopathy, kidney and liver diseases, mental and neurological diseases, obstructive lung diseases, hemostatic disorders and dialysis in patients
  • Addiction to drugs and psychoactive substances and history of drug abuse
  • The presence of infection in the operation site
  • History of taking antidepressants and sedatives and any medicine that changes the perception of pain

Outcomes

Primary Outcomes

Not specified

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