跳至主要内容
临床试验/ACTRN12611001082998
ACTRN12611001082998招募中不适用

Study to determine if the addition of a collagen scaffold device will increase tendon thickness with comparable clinical outcomes over subacromial decompression and/or repair alone in patients with a supraspinatus tear.

Rotation Medical, Inc.0 个研究点目标入组 36 人开始时间: 2011年10月19日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
36

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Treatment

入排标准

年龄范围
40 Years 至 65 Years(—)
性别
All

入选标准

  • Patients requiring surgical rotator cuff treatment of a partial- or small full-thickness tear of the supraspinatus tendon, as determined jointly by the surgeon and the patient.
  • Patients with chronic shoulder pain lasting longer than three months and resistant to pain medication and conservative treatment.
  • Patients over 40 years and under 65 years of age at time of surgery.
  • Patients who understand the conditions of the study and are willing to participate for the length of the prescribed term of follow-up and rehabilitation.
  • Patients who are capable of, and have given informed consent to their participation in the study.

排除标准

  • Patients with instability of the index shoulder.
  • Patients with grade 3 or greater chondromalacia of the index shoulder.
  • Patients who require concomitant procedures other than acromioplasty/subacromial decompression, acromioclavicular joint resection, or biceps tenotomy/tenodesis at least 2 cm distal to the site of supraspinatus tendon treatment.
  • Patients with evidence of calcification of the rotator cuff of the index shoulder.
  • Patients with evidence of grade 2 fatty infiltration or greater of the supraspinatus muscle of the index shoulder on a sagittal view of an MRI scan.
  • Patients with insulin dependent diabetes or other autoimmune or immune deficiency disorders.
  • Patients with genetic collagen disease.
  • Patients with chronic inflammatory disease.
  • Pregnant women or those seeking to become pregnant.
  • Patients who have had previous rotator cuff shoulder surgery on the index shoulder.
  • Patients with a history of oral steroid use in the last 2 months or injectable steroid use in the last 4 weeks.
  • Patients with an inability to complete post-surgery physical therapy or return for follow-up visits.
  • Patients who have been heavy smokers within the last 6 months (more than 20 cigarettes per day).
  • Patients with a known history of hypersensitivity to bovine-derived materials.

研究者

发起方
Rotation Medical, Inc.

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