EUCTR2021-000242-17-DK进行中（未招募）1 期
The effect of the popliteal plexus block on postoperative opioid consumption, pain, muscle strength and mobilization after total knee arthroplasty- a randomized, controlled, blinded study
Region Hospital Silkeborg0 个研究点目标入组 165 人开始时间: 2021年1月27日最近更新:
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 165
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Scheduled to undergo primary total knee arthroplasty in spinal anesthesia
- •Able to perform a Timed Up and Go (TUG) test
- •Age > 50 years old
- •Ability to give their written informed consent to participating in the study after having fully understood the contents of the study
- •American Society of Anesthesiologists (ASA) physical status 1, 2, or 3
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 45
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 120
排除标准
- •Patients who cannot cooperate
- •Patients who cannot understand or speak Danish.
- •Patients with allergy or intolerance to the medicines used in the study
- •Patients with a daily intake of strong opioids (morphine, oxycodone, ketobemidone, methadone, fentanyl)
- •Patients suffering from alcohol and/or drug abuse – based on the investigator's assessment
- •Diagnosed with chronic central or peripheral neurodegenerative disorders
- •Body Mass Index > 40
研究者
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