跳至主要内容
临床试验/NCT01032356
NCT01032356Unknown不适用

Contracture Reduction Following Distal Radius Fracture Surgical Management

Dynasplint Systems, Inc.0 个研究点目标入组 50 人开始时间: 2016年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
50
主要终点
The dependent variable will be change in maximal, active range of motion in extension and the independent variables will include DASH scores and measurements taken from radiographic imaging

研究概览

简要总结

The purpose of this study was to examine the efficacy of dynamic splinting as a therapeutic modality in reducing contracture following surgical treatment of distal radius fractures.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

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

  • •Distal radius fracture treated with surgical management and wrist flexion contracture upon follow up

排除标准

  • •Carpal Fractures (Scaphoid, Lunate, Hamate, and Trapezium)
  • •Radial nerve entrapment
  • •Arthrodesis
  • •Traumatic dislocation of the distal ulna

研究组 & 干预措施

Dynasplint

Experimental

Patients will be treated with the current standard of care and the Wrist Extension Dynasplint.

干预措施: Wrist Extension Dynasplint (Device)

结局指标

主要结局

The dependent variable will be change in maximal, active range of motion in extension and the independent variables will include DASH scores and measurements taken from radiographic imaging

时间窗: 12 weeks

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

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