IRCT20201026049147N1已完成3 期
Evaluating the effect of preoperative sublingual buprenorphine on pain intensity after lumbar disc surgery
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 78
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
- 35 years 至 70 years（—）
- 性别
- All
入选标准
- •Patient candidate for elective discectomy with 1 or 2 lumbar discs
- •With ASA class I and II
- •Age range 35-70
- •Conscious consent to participate in the study
- •Hypersensitivity to buprenorphine
- •Confirmation of diagnosis by physical examination, CT scan and MRI
- •Patient's willingness to participate in the study and obtaining informed consent
排除标准
- •Patient's unwillingness at any time to continue the study
- •Incidence of any uncommon side effects during surgery.
- •Alcohol or drug abuse
- •Opioids use 24 hours prior to intervention
- •Involvement of more than two lumbar disc
研究者
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