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临床试验/CTRI/2022/11/047339
CTRI/2022/11/047339已完成4 期

A retrospective observational study on functional outcomes following arthroscopic Anterior Cruciate Ligament (ACL) reconstruction using loop suture button and/or interference screw of SIRONIX

Healthium Medtech Limited0 个研究点目标入组 33 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
入组人数
33

研究概览

简要总结

暂无简介。

研究设计

研究类型
Pms

入排标准

入选标准

  • 1. Male and female patients aged between 18 to 60 years at the time of surgery
  • 2. Patients who underwent ACL reconstruction using loop suture button and/or HELYSIS interference screw of SIRONIX between April 2018 to July 2022
  • 3. Patients who have provided verbal consent or written informed consent (if subject visits the site) to participate in the study

排除标准

  • 1. Unable to provide verbal consent or written informed consent and unwilling to be followed up telephonically
  • 2. Patients who have suffered traumatic injury after surgery affecting the operated knee
  • 3. Patients who are unable to move/walk due to critical illness other than operated knee complications

研究者

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