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临床试验/NCT03777735
NCT03777735Unknown不适用

Multicentric Observational Study on the Use of a Human Bone Graft in Osteochondral Defects

Medical University of Vienna5 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2018年4月24日最近更新:
适应症

试验速览

阶段
不适用
入组人数
20
试验地点
5
主要终点
incidence of surgical revisions

研究概览

简要总结

This observational study is to document the application of a human bone graft in the surgical repair of bone fragment detachment in the knee joint (osteochondral defect) and its subsequent healing process.

详细描述

For the treatment of bone fractures metal screws have been used for decades. Removal of material is the major disadvantage of conventional osteosynthesis and requires a second intervention, with all the complications and risks for each patient. In order to avoid this second surgery, it is possible to use human bone screw grafts instead of metal screws.

The bone graft helps to create a solid, bony connection. This connection leads to an extension, a bone remodeling, bone installation and optimal reparation process in the affected area.

The comparatively rare occurrence of suitable patients contributes to the fact that there has not been enough systematic research to objectively confirm the benefits of the product, which is why this observational study is being conducted.

In total, 20 patients will be enrolled in several centers in Austria. The low number of cases and the multicenter design is due to the rarity of suitable patients.

This observational study will use Shark Screw® grafts without exception at all participating centers. These grafts are manufactured by two tissue banks, the Austrian Tissue Bank surgebright and the German Institute for Cell and Tissue Replacement (DZIG) and were approved by the competent Austrian authority (AGES) in 2016.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
8 Years 至 99 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Indication for the use of a human bone graft in the surgical treatment of osteochondral defects
  • legal capability of adults, guardians and adolescents aged 14 to 17 years, age-appropriate perceptivity for children 8 to 13 years old
  • Written consent to participation in the study after previous written and oral education (additional consent for participation of minors in the study after prior written and oral education by at least one parent)
  • Age ≥ 8 years

排除标准

  • Insufficient knowledge of the German language
  • Alcohol and drug abuse
  • Pregnant or breastfeeding woman
  • Foreseeable compliance issues
  • Neoplastic diseases, malignant bone tumors, rheumatoid arthritis
  • Active osteomyelitis
  • Ulcerations in the area of the skin of the surgical area
  • Immunosuppressive drugs that can not be discontinued

结局指标

主要结局

incidence of surgical revisions

时间窗: 1 year

Was a surgical revision done postoperatively? YES/NO

incidence of postoperative pseudoarthrosis

时间窗: 1 year

based on x-rays or MRI: Is a postoperative pseudoarthrosis visible? YES/NO

incidence of loosening of the osteochondral fragment

时间窗: 1 year

based on x-rays or MRI: Is a loosening of the osteochondral fragment visible? YES/NO

incidence of loosening of the screw

时间窗: 1 year

based on x-rays or MRI: Is a loosening of the screw visible? YES/NO

incidence of cracking of the osteochondral fragment

时间窗: 1 year

based on x-rays or MRI: Is a cracking of the osteochondral fragment visible? YES/NO

time to healing of the osteochondral fragment

时间窗: 1 year

based on x-rays or MRI: Has the osteochondral fragment healed into the surrounding area? YES/NO

incidence of cracking of the screw

时间窗: 1 year

based on x-rays or MRI: Is a cracking of the screw visible? YES/NO

evaluation postoperative pain (VAS)

时间窗: 1 year

The visual analogue scale (VAS) is a vertical line, 10 centimeters (100 mm) in length, anchored by 2 verbal descriptors, one for each symptom extremes (0mm = no pain - 100mm = worst imaginable pain). A higher score indicates more pain.

duration of postoperative job-related incapacity

时间窗: 1 year

evaluation of duration

次要结局

  • patient satisfaction (VAS)(1 year)
  • Knee Outcome Survey - Activities of Daily Living Scale (KOS-ADL)(1 year)
  • International Knee Documentation Committee Subjective Knee Form (IKDC Score)(1 year)

研究者

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

Catharina Chiari

Univ. Prof. Dr. Catharina Chiari, MSc

Medical University of Vienna

研究点 (5)

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