跳至主要内容
临床试验/NCT00435149
NCT00435149已完成不适用

Post-operative Mobilization for Carpal Tunnel

Vanderbilt University2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2006年12月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
2
主要终点
Function assessment questionnaire score, pain score questionnaire, and measurements will be used to determine outcome.

研究概览

简要总结

This study will investigate the effect of one week of immobilization following carpal tunnel release surgery versus no immobilization.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients undergoing open carpal tunnel release will be included in this study.
  • Patients must have clinical evidence of carpal tunnel syndrome.
  • Patients must have positive EMG results.
  • English speaking patients only.
  • Patient selection factors include:
  • Ability and willingness to follow instructions.
  • Patients who are able and willing to return for follow-up evaluations.
  • Patients of all races and genders.
  • Patients who are able to follow care instructions.

排除标准

  • Patients less than 18 years old.
  • Patients who are pregnant.
  • Patients unwilling or unable to comply with a rehabilitation program for carpal tunnel release who indicate difficulty or inability to return for follow-up visits prescribed by the study protocol.
  • Patients who qualify for inclusion in the study, but refuse consent to participate in the study.

结局指标

主要结局

Function assessment questionnaire score, pain score questionnaire, and measurements will be used to determine outcome.

时间窗: 6 months

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (2)

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