跳至主要内容
临床试验/NCT04312412
NCT04312412招募中不适用

Outcomes of Flexor Tendons Repair in Zones I-III From 2014-2025: a Swiss Multicenter Cohort Study

University of Zurich1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2014年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
500
试验地点
1
主要终点
Grip or pinch strength

研究概览

简要总结

In order to gather enough data for meaningful statistics, a multicenter register of all flexor tendon repairs was established with surgical, clinical and rehabilitation patient data. The controlled active motion (CAM) protocol was administered in all patients after surgery. The purpose was to (i) measure surgery and therapy outcomes in the three centers and (ii) evaluate potential influencing factors on outcomes.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Injury between 2014 and 2025
  • Flexor tendon injury of the fingers or thumb in zones 1-3

排除标准

  • No given consent
  • Concomitant injuries as fractures, large soft tissue injuries, replantation
  • Bony avulsion fracture of flexor tendon (Jersey finger)
  • Basic disease as rheumatoid diseases
  • Primary and secondary tendon reconstruction and tendon transfer

结局指标

主要结局

Grip or pinch strength

时间窗: 52 weeks

Strength

Time return to work

时间窗: 52 weeks

off work time

Range of motion

时间窗: 52 weeks

Total active motion

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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