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临床试验/NCT02645097
NCT02645097已完成不适用

Ideal Anatomic Location for Saphenous Nerve Blocks: A Prospective Clinical Evaluation

Paul J. Juliano, M.D.2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2014年7月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30
试验地点
2
主要终点
knee extensor strength measured in kilograms

研究概览

简要总结

This research is being done to compare two different saphenous nerve block locations and will help to determine which site best maintains knee strength and pain control.

详细描述

This is a prospective, randomized, observer blinded clinical trial comparing motor strength in knee extension between two sets of patients, one receiving a proximal thigh block of the saphenous nerve and one receiving a distal thigh block of the saphenous nerve. The secondary objectives are to compare the pain relief and quality of life of participants in these two groups.

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 (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18-65
  • Upcoming elective foot or ankle surgery

排除标准

  • Preoperative weakness in knee extension
  • Documented neuropathy
  • Previous knee surgery
  • Inability to provide informed consent

研究组 & 干预措施

Proximal saphenous nerve block

Active Comparator

The anesthesiologist will administer a saphenous proximal nerve block if specified in the randomization envelope.

干预措施: Saphenous Nerve Block (Procedure)

Distal saphenous nerve block

Active Comparator

The anesthesiologist will administer a saphenous distal nerve block if specified in the randomization envelope.

干预措施: Saphenous Nerve Block (Procedure)

结局指标

主要结局

knee extensor strength measured in kilograms

时间窗: change from baseline preoperatively to 30 minutes after nerve block placement

Strength of the knee extensors in both treatment arms (distal vs. proximal block) will be tested preoperatively and again 30 minutes after the nerve block by using a hand-held dynamometer measured in kilograms

次要结局

  • quality of life assessment(change from baseline preoperatively to two weeks post-operatively)
  • pain level(change from baseline preoperatively to two weeks post-operatively)

研究者

发起方
Paul J. Juliano, M.D.
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Paul J. Juliano, M.D.

Professor of Orthopaedic Surgery

Milton S. Hershey Medical Center

研究点 (2)

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