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临床试验/NCT03228849
NCT03228849已完成不适用

Conservative Management Equally Effective to New Suture Anchor Technique for Acute Mallet Finger Deformity: A Prospective Randomized Clinical Trial

Istanbul University2 个研究点 分布在 1 个国家目标入组 29 人开始时间: 2013年6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
入组人数
29
试验地点
2
主要终点
Extension deficit

研究概览

简要总结

This study aims to compare conservative treatment versus a new suture anchor technique for bony mallet finger in 29 patients.

详细描述

This study aims to compare conservative treatment versus a new suture anchor technique for bony mallet finger in 29 patients who presented to investigators' clinic between 2013 and 2015. Patients were randomly assigned to conservative or surgical treatment groups. Patients in the conservative group were followed with immobilization with aluminum splint and physical therapy. Patients in the surgical group were treated with investigators' new surgical suture anchor technique and then received physical therapy. The patients were followed for 12 months. Primary study outcomes were extension deficit, days to return to work and DIP flexion.

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
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Wehbe Schneider type 1 - 2 and type A - B fractures
  • ability to provide closed reduction
  • patients' voluntariness

排除标准

  • Wehbe Schneider type C and type 3 fractures

研究组 & 干预措施

Conservative Treatment

Active Comparator

Patients were treated with 6 weeks with splinting and were then started on physical therapy for 2 weeks.

干预措施: Conservative Treatment (Procedure)

Surgical Treatment

Active Comparator

Patients were treated with the new suture anchor technique and after 6 weeks were started on physical therapy for 2 weeks.

干预措施: Suture anchor technique (Procedure)

结局指标

主要结局

Extension deficit

时间窗: 12 months

The inability to actively extend DIP joint to 0 degrees.

DIP flexion

时间窗: 12 months

The maximum angle of flexion at DIP joint

Days to return to work

时间窗: Starting from the date of the start of treatment until patients returns to work, assessed up to 12 months

Time to return to work

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Hayati Durmaz

Professor, MD

Istanbul University

研究点 (2)

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