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临床试验/NCT02037204
NCT02037204已完成1 期

Instant MSC Product Accompanying Autologous Chondron Transplantation (IMPACT): Safety and Feasibility of a Single-stage Procedure for Focal Cartilage Lesions of the Knee.

UMC Utrecht2 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2013年3月最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
发起方
UMC Utrecht
入组人数
35
试验地点
2
主要终点
Safety: Adverse Events

研究概览

简要总结

Articular cartilage defects in the knee have a poor intrinsic healing capacity and may lead to functional disability and osteoarthritis. Cartilage cell therapy using autologous chondrocyte implantation (ACI) has been established as the first advanced treatment therapy medicinal product. Although this technique has achieved good mid-term results, it is a costly and extensive two-stage procedure which is limited by the number of chondrocytes obtained by biopsy and the dedifferentiation resulting from the expansion phase. Therefore, there is a need for improvement. A new cartilage repair technique should aim at decreasing surgical trauma, lowering complexity, improving logistics and cost-effectiveness while retaining or improving clinical outcome. Direct contact between mesenchymal stromal cells (MSCs) and dedifferentiated articular chondrocytes in vitro showed improvement of the chondrogenic phenotype of dedifferentiated articular chondrocytes. In addition, preserving the pericellular matrix of chondrocytes improves cartilage formation. These chondrons (chondrocytes with their pericellular matrix) have shown improved cartilage formation when combined with allogeneic MSCs in extensive preclinical studies. The cells are mixed with fibrin cell carrier and applied to the cartilage lesion within one surgical procedure. This will reduce patient morbidity and improve patient care through immediate transplantation of a potent cell-based cartilage product. This is a phase I/II prospective monocenter study to evaluate the safety and feasibility of the IMPACT for treatment of focal articular cartilage lesions of the knee.

研究设计

研究类型
Interventional
分配方式
Na
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 45 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age >18 and <45 years old
  • Symptomatic isolated full-thickness articular cartilage lesion on the femoral condyle or trochlea.
  • Size 2 - 8 cm2
  • Intact anterior cruciate ligament

排除标准

  • (History of) osteoarthritis, defined as Kellgren-Lawrence grade >3 as determined from appropriate X-ray.
  • Concomitant inflammatory disease that affects the joint (rheumatoid arthritis, metabolic bone disease, psoriasis, gout, symptomatic chondrocalcinosis)
  • (History of) Septic arthritis.
  • Malalignment requiring an osteotomy.
  • (History of) total menisectomy in the target knee joint.
  • Any surgery in the knee joint 6 months prior to study inclusion.
  • Risk groups for MRI scanning due to the magnetic field like patients with pacemakers, nerve stimulators, metal particles, stents, clips or implants, (possible) pregnancy or breast feeding.
  • Patients with severe anxiety for MRI scans and/or needles

研究组 & 干预措施

Cartilage repair surgery

Experimental

Single-stage cartilage repair surgery using autologous chondrons (10-20%) and allogeneic MSCs (80-90%) in a fibrin glue carrier with a dosage of two million cells/ cm2 applied once during a surgical procedure.

干预措施: Cartilage repair surgery (Other)

结局指标

主要结局

Safety: Adverse Events

时间窗: 18 months

Adverse events rate

次要结局

  • Clinical Improvement, Knee Injury and Osteoarthritis Outcome Score(3 and 18 months)

研究者

发起方
UMC Utrecht
申办方类型
Other
责任方
Principal Investigator
主要研究者

D.B.F. Saris

MD, PhD, Orthopaedic surgeon

UMC Utrecht

研究点 (2)

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