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临床试验/NCT00158613
NCT00158613已完成4 期

A Prospective, Longitudinal Within-Patient Evaluation of the Effectiveness (Durability) of Carticel® (Autologous Cultured Chondrocytes) Compared to Non-Carticel Surgical Treatment for Articular Cartilage Defects of the Knee.

Vericel Corporation56 个研究点 分布在 2 个国家目标入组 126 人开始时间: 2000年3月最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
126
试验地点
56
主要终点
Mean change from baseline in the KOOS

研究概览

简要总结

This study is a prospective, longitudinal, multi-center, within patient evaluation of patients with articular cartilage defects of the knee who have had an inadequate response to a prior non-Carticel surgical treatment. Patients who met eligibility criteria were enrolled in the study. Subsequent to implantation with Carticel patients have follow-up every 6-months up to 48-months.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Provided written informed consent
  • Documented history of at least one Grade III or Grade IV defect (modified Outerbridge classification) on the medial or lateral femoral condyle or trochlea
  • Failed prior treatment for articular cartilage defects of the knee, e.g. inadequate response to a non- ACI surgical procedure to treat the lesion, within past 3 yrs
  • Patient reported overall knee condition of 5 or less on the Modified Cinn Rating System
  • patients must have had a cartilage defect located on the medial or lateral femoral condyle or trochlea which had an inadequate response to a prior arthroscopic or other non-Carticel surgical repair procedure

排除标准

  • see above

结局指标

主要结局

Mean change from baseline in the KOOS

时间窗: Baseline, 6 month, 12 months, 24 months, 36 months, 48 months

次要结局

  • Change from Baseline in the Modified Cincinnati Score(6mo, 12mo, 18mo, 24mo, 30mo, 36mo, 42mo, 48mo)
  • Change from Baseline in the Knee injury and Osteoarthritis Outcome Score (KOOS)Which consists of five sub- categories = Pain, ADL, QOL, Symptoms, Sport(12mo, 24mo, 36mo, 48mo)
  • Change from Baseline in the SF-36 Health Status Survey(12mo, 24mo, 36mo, 48mo)

研究者

申办方类型
Industry

研究点 (56)

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Study of the Treatment of Articular Repair (STAR) | 临床试验