跳至主要内容
临床试验/NCT05867355
NCT05867355招募中不适用

A Multi-Centre Prospective Cohort Study of Surgically Treated Displaced Mid-diaphyseal Clavicle Fractures

University of Calgary1 个研究点 分布在 1 个国家目标入组 111 人开始时间: 2021年3月22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
111
试验地点
1
主要终点
Identify rationale for implant removal

研究概览

简要总结

This prospective, multi-centre study aims to determine clinical, radiographic, and patient-reported outcomes (PROMs) following surgical fixation of displaced mid-diaphyseal clavicle fractures and to compare implant removal rates between techniques within 2-years of the procedure.

详细描述

Given the substantially lower implant removal rate in combination with a high union rate with the dual mini-fragment technique, we do not believe there is clinical equipoise required for a randomized clinical trial.

This study is a multi-centre, prospective cohort study (11 sites confirmed to date) of all operatively treated clavicle fractures, in order to objectively evaluate all current surgical techniques used across Canada. This pragmatic approach will allow us to observe surgical decision-making, rationale for implant removal, and report on clinical, radiographic, and patient-reported outcomes for all techniques over a 2-year follow-up timeframe, for the first time.

All enrolled patients will be encouraged to begin immediate range of motion as tolerated and weightbearing as tolerated post-operatively. This will be assessed at each follow-up and any reason for delayed motion or weightbearing will be reported.

研究设计

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

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

  • Treated with surgical fixation for a displace mid-diaphyseal clavicle fracture.
  • Aged 18 years of age or older and skeletally mature.
  • Enrolled within 21 (+3 days) of injury.
  • Willing and able to complete consent and study participation.

排除标准

  • Pathological fractures.
  • Clavicle non-unions.
  • Current or prior ipsilateral upper extremity injury that may impact functional outcomes.
  • Polytrauma patients with injuries projected to affect rehabilitation course.
  • Active malignancy.
  • Inability to provide consent or complete follow-up.
  • Incarcerated patients.

结局指标

主要结局

Identify rationale for implant removal

时间窗: 4 years

To report rationale for implant removal in an appropriately powered prospective cohort study.

Determine implant removal rates

时间窗: 4 years

To report implant removal rates in an appropriately powered prospective cohort study.

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

Prism Schneider

Orthopedic Trauma Research Lead

University of Calgary

研究点 (1)

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