IRCT20220727055567N1招募中2 期
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
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 入组人数
- 44
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 years 至 no limit（—）
- 性别
- All
入选标准
- •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
排除标准
- •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
研究者
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