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
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.
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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