NCT01593566已完成4 期
Femoral Nerve Block Using 0.25% Versus 0.5% Bupivacaine for Analgesia After Arthroscopic Anterior Cruciate Ligament Reconstruction
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- time to first analgesic requirement
研究概览
简要总结
Femoral nerve block using 0.25% bupivacaine or 0.5% bupivacaine provides a longer time for analgesia after Anterior Cruciate Ligament (ACL) reconstruction.
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 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients scheduled for ACL reconstruction
- •ASA physical status I-II
- •Body weight > or = 50 kg.
排除标准
- •Patients with redo ACL reconstruction
- •Contraindication to neuraxial block
- •allergy to local anesthetics, sulfa, NSAIDs, morphine, paracetamol
- •Patients with communication problem
研究组 & 干预措施
0.25% bupivacaine
Active Comparator
femoral nerve block using 0.25% bupivacaine versus 0.5% bupivacaine
干预措施: 0.25% Bupivacaine (Drug)
0.5% bupivacaine
Active Comparator
femoral nerve block using 0.25% bupivacaine versus 0.5% bupivacaine
干预措施: 0.5% Bupivacaine (Drug)
结局指标
主要结局
time to first analgesic requirement
时间窗: 48 hr
次要结局
- pain score scale(48 hr)
研究者
arissara iamaroon
associated professor
Mahidol University
研究点 (1)
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