NCT01459861终止不适用
Assessment of Early Ambulation in Patients Receiving Continuous Adductor Canal Block With Ultrasound Guided Posterior Capsular Knee Injection vs. Femoral Nerve Block With Tibial Nerve Block Following Total Knee Replacement
Trinity Health Of New England2 个研究点 分布在 1 个国家目标入组 11 人开始时间: 2011年10月1日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 发起方
- 入组人数
- 11
- 试验地点
- 2
- 主要终点
- Ability to ambulate post operatively.
研究概览
简要总结
The purpose of this study is to assess early ambulation following total knee replacement in patients receiving continuous adductor canal block with posterior capsular injection compared to continuous femoral nerve block with tibial nerve block.
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
- Single (Care Provider)
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
- 否
入选标准
- •knee arthroplasty
- •ages 18-80
排除标准
- •history of neurological disease
- •pregnancy
- •neuropathy
- •chronic narcotic use
- •allergy to local anesthetic solution or NSAIDS
- •inability to give consent or cooperate with the study protocol
结局指标
主要结局
Ability to ambulate post operatively.
时间窗: Up to 3 days (72 hours) post surgery.
Ability to ambulate and perform tasks of the rehabilitation program and reach rehabilitation milestones after total knee arthroplasty.
次要结局
- Pain scores at rest and with knee flexion.(Up to 3 days ( 72 hours) after surgery)
- Pain Medication Consumption(Up to 3 days (72 hours) post surgery)
研究者
研究点 (2)
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