跳至主要内容
临床试验/NCT04965103
NCT04965103已完成不适用

Graft Reconstruction for Irreparable Rotator Cuff Tears: Superior Capsule Reconstruction or Tendon Repair With Graft Interposition

University of Calgary0 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

试验速览

阶段
不适用
状态
已完成
入组人数
50
主要终点
American Shoulder and Elbow Surgeon Outcome - patient portion

研究概览

简要总结

Randomized controlled trial examining superior capsule reconstruction versus tendon repair with graft interposition in "irreparable" rotator cuff tears.

详细描述

RCT n = 50

Groups:

  1. bridging
  2. SCR

Outcomes:

  1. WORC
  2. ASES
  3. QuickDASH
  4. MRI at 12 months post-op

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
Double (Participant, Outcomes Assessor)

盲法说明

Participant and research assistant collecting outcomes were blinded.

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

  • Large to massive rotator cuff tear (with or without subscapularis tear) that may possibly be irreparable without the use of graft materials (confirmed intra-operatively)
  • Either primary tear or re-tear after previous repair
  • Radiographic evidence of Hamada stage 1-3, with or without Samilson & Prieto mild osteoarthritis (<3mm inferior osteophyte)

排除标准

  • Primary glenohumeral osteoarthritis: radiographic evidence of Samilson & Prieto classification moderate or greater
  • Cuff tear arthropathy (CTA): radiographic evidence of Hamada stage 4 or above
  • Inflammatory joint disease of the shoulder (e.g. rheumatoid arthritis)
  • Medical issues precluding surgery
  • Unwilling or unable to complete study outcomes
  • Worker's Compensation Claim or litigation

结局指标

主要结局

American Shoulder and Elbow Surgeon Outcome - patient portion

时间窗: 3 months

American Shoulder and Elbow Surgeon Outcome - patient portion (minimum score = 0, maximum score = 100, best outcome = 100)

次要结局

  • Tendon healing, assessed via MRI(12 months)
  • Western Ontario Rotator Cuff Index(3 months)
  • Disabilities of the Arm, Shoulder and Hand - QuickDASH(3 months)

研究者

申办方类型
Other
责任方
Sponsor

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