Instant MSC Product Accompanying Autologous Chondron Transplantation (IMPACT): Safety and Feasibility of a Single-stage Procedure for Focal Cartilage Lesions of the Knee.
Trial Snapshot
- Phase
- Phase 1
- Status
- Completed
- Sponsor
- UMC Utrecht
- Enrollment
- 35
- Locations
- 1
- Primary Endpoint
- Safety: Adverse Events
Study Overview
Brief Summary
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.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 45 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •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
Exclusion Criteria
- •(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
Arms & Interventions
Cartilage repair surgery
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.
Intervention: Cartilage repair surgery (Other)
Outcomes
Primary Outcomes
Safety: Adverse Events
Time Frame: 18 months
Adverse events rate
Secondary Outcomes
- Clinical Improvement, Knee Injury and Osteoarthritis Outcome Score(3 and 18 months)
Investigators
D.B.F. Saris
MD, PhD, Orthopaedic surgeon
UMC Utrecht
