KCT0004766终止未知
The effectiveness of multiple atelocollagen injection in partial thickness rotator cuff tear
试验速览
- 阶段
- 未知
- 状态
- 终止
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational Study
入排标准
- 年龄范围
- 30(Year) 至 69(Year)(—)
- 性别
- All
入选标准
- •Inclusion Criteria
- •1)Adults over 30 and under 70
- •2)Partial thickness rotator cuff tear diagnosed by imaging test (ultrasound or MRI)
- •3)Patients who have been treated for more than 3 months by medication or physical therapy but have not improved
- •4)If the concomitant medication continues to be administered during the trial, patients who have confirmed the correct prescription drug being taken within at least one week and agreed to maintain a constant amount as before injection during the study
- •5)patients who understand the study, agree to participate in the study, and have their own written consent
排除标准
- •Exclusion Criteria
- •1)Patients with previous history of injection therapy within 6 weeks
- •2)Patients with Adhesive capsulitis
- •3)Full thickness rotator cuff tears diagnosed by MRI or ultrasound
- •4)Patients with a history of uncontrolled diabetes, infectious arthritis, rheumatoid arthritis, tumors, fractures, degenerative arthritis
- •5)Patients who refuse injection
- •6)Patients who want surgical treatment
- •7)Patients with hypersensitivity to collagen
- •8)Pregnant or lactating or planning to become pregnant
- •9)Patients expected to have complications because of anticoagulants therapy
- •10)Patients sensitive to pig protein
- •11)Patients with a history of radiotherapy and chemotherapy within the past 2 years (except when it is determined that collagen can be administered as judged by a clinician)
- •12)Patients or family members with autoimmune disease in progress or with past military service
- •13)Patients who are sensitive to implants
- •14)Any clinically significant health abnormalities that can affect the completion of the study
- •15)Patients deemed inappropriate for this study by the judgment of doctor such as mental illness
研究者
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