jRCT1030250650尚未招募不适用
A double-blind randomized controlled trial to evaluate the efficacy of combined femoral nerve block and selective tibial nerve block for postoperative pain management in high tibial osteotomy.
未提供0 个研究点目标入组 60 人开始时间: 待定
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
入排标准
- 年龄范围
- 20age old over 至 No limit（—）
- 性别
- All
入选标准
- •Patients undergoing medial open wedge high tibial osteotomy at our hospital.
- •Patients over 20 years
- •Patients who receive written informed consent.
- •Patients with American Society of Anesthesiologists physical status classification 1-3.
排除标准
- •Patients who are deemed inappropriate as research subjects by the principal investigator
- •Patients who refuse to participate in the study.
- •Patients who have contraindications to the use of usual postoperative analgesics such as NSAIDs and acetaminophen, contraindications to local anesthetics, are pregnant or suspected pregnant women, poorly controlled diabetes, unable to understand the perioperative questionnaire (language or cognitive impairment), severe heart disease, Severe obesity (BMI > 35), patients who have not responded to nerve blocks, emergency surgery.
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