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临床试验/NCT03061942
NCT03061942已完成不适用

Arthroscopic Rotator Cuff Repair With Synovectomy; Prospective Randomized Controlled Study

Seoul National University Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2017年3月8日最近更新:
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
60
试验地点
1
主要终点
The worst pain VAS(visual analogue scale)

研究概览

简要总结

The purpose of this study is to assess the effect of synovectomy on clinical outcomes of arthroscopic rotator cuff repair.

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)

入排标准

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

入选标准

  • Patients with a full-thickness rotator cuff tear undergoing arthroscopic rotator cuff repair

排除标准

  • History of shoulder surgery
  • Acute trauma on affected shoulder
  • Chronic dislocation
  • Pyogenic infection
  • Rotator cuff arthropathy with glenohumeral osteoarthritis and superior migration of the humeral head
  • Isolated subscapularis tear
  • Psychiatric problems that precluded informed consent
  • An inability to read or write
  • Other serious issues that precluded participation in the study
  • Open surgery
  • Rotator cuff tear with worker's compensation claim
  • Refuse to participate in the study
  • LOM that need brisement force
  • Partial-thickness tear with focal full-thickness extension
  • Irrepairable rotator cuff tear
  • Subjects who, for any reason, are judged by the investigator to be inappropriate for this study, including a subject who had other severe medical condition or laboratory abnormality, or who is unable to communicate or to cooperate with the investigator

研究组 & 干预措施

Conventional

Active Comparator

Arthroscopic rotator cuff repair without synovectomy

干预措施: Arthroscopic rotator cuff repair without synovectomy (Other)

Synovectomy

Experimental

Arthroscopic rotator cuff repair with synovectomy

干预措施: Arthroscopic rotator cuff repair with synovectomy (Other)

结局指标

主要结局

The worst pain VAS(visual analogue scale)

时间窗: at 3 months after surgery

A 10-cm scale marked from ''no pain''(0) to ''unbearable pain''(10) was used.

次要结局

  • The average pain VAS(visual analogue scale)(at 3 months after surgery)
  • Constant-Murley score(at 3 months after surgery)

研究者

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

Hyunchul Jo

Associate professor

Seoul National University Hospital

研究点 (1)

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