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临床试验/NCT05615259
NCT05615259
招募中
不适用

A Prospective, Multi-Center, Randomized Clinical Study of Total Shoulder Arthroplasty Comparing Exactech Guided Personalized Surgery (GPS) vs. Conventional Instrumentation

Exactech1 个研究点 分布在 1 个国家目标入组 260 人2020年9月23日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Technology
发起方
Exactech
入组人数
260
试验地点
1
主要终点
Constant
状态
招募中
最后更新
去年

概览

简要总结

The primary objective of this study is to examine the optimization of Reverse Shouder Arthroplasty implant position between GPS and conventional techniques. The secondary objective is to assess the effect of implant position using GPS vs. conventional techniques on ROM and patient reported outcomes. Long-term follow-up to 10 years with minimum 2 year follow-up for patients.

注册库
clinicaltrials.gov
开始日期
2020年9月23日
结束日期
2031年9月30日
最后更新
去年
研究类型
Observational
性别
All

研究者

发起方
Exactech
责任方
Sponsor

入排标准

入选标准

  • Patient is at least 21 years of age at the time of surgery
  • Patient is indicated for reverse shoulder arthroplasty
  • Patient is willing to participate by complying with pre- and postoperative visit requirements
  • Patient is willing to participate for the entire length of the prescribed follow-up (minimum 2 years)
  • Patient is willing and able to review and sign a study informed consent form
  • Preop CT scan is within 3 months of the date of surgery

排除标准

  • Revision shoulder arthroplasty
  • Reverse shoulder arthroplasty for fracture
  • Need for structural glenoid bone graft
  • Osteomyelitis of the proximal humerus or scapula; if a systemic infection or a secondary remote infection is suspected or confirmed, implantation should be delayed until infection is resolved
  • Inadequate or malformed bone that precludes adequate support or fixation of the prosthesis
  • Neuromuscular disorders that do not allow control of the joint
  • Significant injury to the brachial plexus
  • Non-functional deltoid muscles
  • The patient is unwilling or unable to comply with the post-operative care instructions
  • Patients who are a known drug or alcohol abuser, or have a psychological disorder (e.g. schizophrenia major depression, bipolar disorder, etc.) as defined by the DSM4 that affect follow-up care or treatment outcomes.

结局指标

主要结局

Constant

时间窗: Through study completion, an average of 1 per year

Constant Shoulder Score - 100 points scale about pain, Activities of daily living, Strength test, and Range of Motions questions about shoulder where 100 % corresponds to the highest pain

SPADI

时间窗: Through study completion, an average of 1 per year

Shoulder Pain and Disability Index (SPADI) -13 questions assessing about pain scale (5 questions) and disability scale (8 questions) where 0 indicates no pain/no difficulty and 10 indicates worst pain imaginable/so difficult it requires help while performin these activities

ASES

时间窗: Through study completion, an average of 1 per year

American Shoulder and Elbow Surgeons Score (ASES) - 100 points scale about shoulder pain and performance evaluation in activities of daily living where 100 indicates the best shoulder condition

UCLA

时间窗: Through study completion, an average of 1 per year

University of California Los Angeles Shoulder Score (UCLA) - 5 Items score which combines both physician (3 items) and patient assessment (2 items) whith a total range from 0-35 where 0 indicates worse shoulder function and 35 better shoulder function outcomes

SST-12

时间窗: Through study completion, an average of 1 per year

Shoulder Simple Test (SST) - 12 questions with yes/no responses that measure shoulder pain and function from a patient's perspective - 12 yes corresponds to 100%

研究点 (1)

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