Mesenchymal Stem Cells in a Clinical Trial to Heal Articular Cartilage Defects
NCT ID: NCT00885729
Last Updated: 2015-10-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
PHASE1
50 participants
INTERVENTIONAL
2009-04-30
2018-07-31
Brief Summary
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* Compare the treatment efficacy of autologous mesenchymal stem cells (Mesenchymal Stem Cells) versus chondrocytes implanted in a commercial available scaffold in a human clinical trial.
* Determine the effects of specific three months strength training program preoperatively to improve knee function and possible postpone the need of cartilage repair surgery.
* Determine if degenerative changes occur in the knee joints following cartilage repair. This question will be investigated in the proposed clinical trial.
* Determine the characteristics of patients treated either by surgery or by rehabilitation in a long-term follow-up (1, 5 years).
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Stem cells
Cartilage defect are treated surgical either with chondrocytes or stem cells
stem cells
Stem cells or chondrocytes under a commercial available membrane
Chondrocytes
Implantation of chondrocytes
Rehabilitation
Active rehabilitation program
Rehabilitation program
Strength exercises, neuromuscular exercises
Interventions
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stem cells
Stem cells or chondrocytes under a commercial available membrane
Chondrocytes
Implantation of chondrocytes
Rehabilitation program
Strength exercises, neuromuscular exercises
Eligibility Criteria
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Inclusion Criteria
* A full-thickness cartilage lesion (diameter \> 15 mm, but less than 6 cm2 and Lysholm score \< 75 points) located on the femoral condyle
Exclusion Criteria
* Other knee pathology such as ACL injury or a nontreated meniscus injury will not be included in the study to avoid the impact of these knee pathologies on the final results
18 Years
50 Years
ALL
Yes
Sponsors
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University Hospital, Akershus
OTHER
Responsible Party
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Asbjorn Aroen
MD, PhD
Principal Investigators
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Lars Engebretsen, MD,PhD
Role: STUDY_CHAIR
Professor
Locations
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Oslo UniversityHospital-Ullevaal
Oslo, Oslo County, Norway
Countries
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References
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Aroen A, Brogger H, Rotterud JH, Sivertsen EA, Engebretsen L, Risberg MA. Evaluation of focal cartilage lesions of the knee using MRI T2 mapping and delayed Gadolinium Enhanced MRI of Cartilage (dGEMRIC). BMC Musculoskelet Disord. 2016 Feb 11;17:73. doi: 10.1186/s12891-016-0941-y.
Rotterud JH, Reinholt FP, Beckstrom KJ, Risberg MA, Aroen A. Relationship between CTX-II and patient characteristics, patient-reported outcome, muscle strength, and rehabilitation in patients with a focal cartilage lesion of the knee: a prospective exploratory cohort study of 48 patients. BMC Musculoskelet Disord. 2014 Mar 24;15:99. doi: 10.1186/1471-2474-15-99.
Wondrasch B, Aroen A, Rotterud JH, Hoysveen T, Bolstad K, Risberg MA. The feasibility of a 3-month active rehabilitation program for patients with knee full-thickness articular cartilage lesions: the Oslo Cartilage Active Rehabilitation and Education Study. J Orthop Sports Phys Ther. 2013 May;43(5):310-24. doi: 10.2519/jospt.2013.4354. Epub 2013 Mar 13.
Other Identifiers
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S-0738c 2009
Identifier Type: -
Identifier Source: org_study_id
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