NCT01254825已完成4 期
The Efficacy of Adductor-Canal-Block (ACB) in Patients After Knee Arthroscopy
Glostrup University Hospital, Copenhagen2 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2010年11月1日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 72
- 试验地点
- 2
- 主要终点
- Pain-Score (VAS) - patient standing
研究概览
简要总结
The Purpose of this study is to determine whether Adductor-Canal-Block (ACB) is superior to placebo when it comes to analgetic efficacy after Knee-Arthroscopy.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •18-80 years
- •Knee-arthroscopy
- •Written consent
- •ASA I-III
- •BMI 19-35
排除标准
- •Unable to communicate in Danish
- •Allergic reactions toward drugs used in the trial
- •Pregnancy
- •Abuse of alcohol/drugs
- •Daily opioid intake
- •Infection at injection site
- •Can not be mobilised to 5 meters of walk; pre-surgery
结局指标
主要结局
Pain-Score (VAS) - patient standing
时间窗: 2 hours postoperative
Pain-score messured on a Visual Analog Scale (VAS) 2 hours after adductor canal block. Patient standing. Intervention-group vs. placebo-group.
次要结局
- Pain-score (VAS), patient standing(1,2,4,6,8,24 hours postoperative)
- Pain-score (VAS), patient at rest(0,1,2,4,6,8,24 hours postoperative)
- Pain-score (VAS), after 5 meters of walk(2,4,6,8,24 hours postoperative)
- Total Opioid-consumption(0-24 hours postoperative)
- Opioid-consumption, postoperative(0-2, 2-4, 4-6, 6-8, 8-24 hours postoperative)
- Postoperative Nausea and vomiting(0-1, 1-2, 2-4, 4-6, 6-8, 8-24 hours postoperative)
- Postoperative ondansetron consumption(In-hospital)
- Sedation(0,1,2,4,6,8,24 hours postoperative)
研究者
Malene Espelund
MD
Glostrup University Hospital, Copenhagen
研究点 (2)
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