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临床试验/NCT01601951
NCT01601951已完成不适用

Autologous Bone Marrow Concentrate Database Outcomes Research Project

Regenerative Pain Center, Illinois1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2012年4月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
12
试验地点
1
主要终点
Visual Analog Pain Scale

研究概览

简要总结

The purpose of this study is to determine if Bone Marrow Concentrate may be successful in the treatment of osteoarthritis. Bone Marrow Concentrate is known to contain a community of cells that has been shown to have "regenerative" properties. This study is designed to evaluate the short-term clinical and x-ray outcomes of injections for hip and knee osteoarthritis.

Inclusion Criteria:

  • Subjects must be scheduled for an autologous bone marrow hip or knee injection
  • Subjects must have a diagnosis of hip or knee osteoarthritis
  • Subjects must be between the ages of 18 and 85
  • Subjects must be willing and able to sign Informed Consent
  • Subjects must be willing and able to return for scheduled follow-up evaluations

Exclusion Criteria:

  • Subjects who have had any type of visco-supplementation in the treated joint within the last three months prior to enrollment
  • Subjects for whom baseline data is not available

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
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects must be scheduled for an autologous bone marrow hip or knee injection
  • Subjects must have a diagnosis of hip or knee osteoarthritis
  • Subjects must be between the ages of 18 and 85
  • Subjects must be willing and able to sign Informed Consent
  • Subjects must be willing and able to return for scheduled follow-up evaluations

排除标准

  • Subjects who have had any type of visco-supplementation in the treated joint within the last three months prior to enrollment
  • Subjects for whom baseline data is not available

结局指标

主要结局

Visual Analog Pain Scale

时间窗: Baseline, 6 weeks, 3 months, 1 year

Change in subjective pain measure

Harris Hip Score or Knee Society Score

时间窗: Baeline, 6 weeks, 3 months, 1 year

Change in subjective pain, function, functional activity measurement and a clinical physical exam

Physician Global Assessment

时间窗: Baseline, 6 weeks, 3 months, 1 year

Change in physician rated disease activity measurement

次要结局

  • Radiologic(Baseline, 1 year)

研究者

发起方
Regenerative Pain Center, Illinois
申办方类型
Other
责任方
Sponsor

研究点 (1)

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