- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07641868
Management of Focal Cartilage Lesions of the Knee: The Benefits of an Autograft Procedure (CART-MCI Knee)
Cartilage is a tissue whose primary function is to transmit and distribute loads when joints are under stress. It acts as a buffer between bones at the joints. Over time, or due to diseases and/or trauma, this surface can disappear, leading to pain and limited movement. Cartilage lesions are particularly difficult to treat because cartilage has a limited capacity for regeneration.
When cartilage lesions are characterized by a localized defect, several surgical techniques are available to restore cartilage tissue to the affected area.
The most frequently used surgical technique is bone marrow stimulation, also known as microfracture. The cartilage lesion is debrided, the subchondral bone exposed, and then a punch is used to perforate the subchondral bone, allowing a clot to form within the defect. This clot will proliferate and differentiate into scar tissue. However, this cellular differentiation results in fibrocartilaginous tissue rather than hyaline cartilage, sometimes with disappointing clinical outcomes.
Other techniques for cartilage restoration exist and are used routinely, including more biological techniques such as Minced Cartilage Implantation (MCI). Autologous cartilage is first harvested from around the defect, chopped into very small fragments, and then reimplanted. Cartilage fragmentation activates cell proliferation and migration, followed by the synthesis of an extracellular, cartilaginous matrix. The effectiveness of this fragmentation is increased with fine fragments (<0.3 mm). Cell proliferation and activity appear to be stimulated by the systematic addition of PRP (Platelet-Rich Plasma) during the MCI procedure.
The expected benefit of an MCI approach lies in clinical improvement and better cartilage regeneration (observed on imaging) compared to microfracture.
The objective is to conduct a controlled, randomized, blinded study (blinded to both the patient and the MRI assessor of the bone graft) to determine the benefit of an MCI approach versus microfracture.
Panoramica dello studio
Stato
Condizioni
Descrizione dettagliata
Objective : Primary objective: To demonstrate the benefit of the MCI approach in terms of lesion filling at 24 months post-surgery.
Secondary objectives:
- To demonstrate the clinical benefit (based on functional scores and the need for re-intervention) of the MCI approach at different follow-up visits.
- To describe all post-operative complications.
- To demonstrate the benefit of the MCI approach in terms of lesion filling at 24 months post-surgery in patients with lesions larger than 2 cm².
Outcome Measures :
Primary endpoint: Bone grafting will be measured by magnetic resonance imaging at 24 months using the MOCART score (Magnetic Resonance Observation of Cartilage Repair Tissue 2.0 Knee Score), which assesses the rate and quality of grafting. The evaluator will be blinded to the randomization arm.
Secondary endpoints:
- Functional scores at baseline, at 3, 9, and 24 months:
- Visual Analog Scale (VAS)
- Self Knee Value (SKV)
- Knee Injury and Osteoarthritis Outcome Score (KOOS score)
- and Tegner-Lysholm activity score
- Postoperative complications from all causes at each visit
- Need for reoperation at 3, 9, and 24 months post-surgery.
Single-center, controlled, randomized, blinded (patient and MRI assessor blinded), two parallel arms with a 1:1 ratio:
- Arm 1: Microfractures
- Arm 2: Minced Cartilage Implantation (MCI)
Randomization will be stratified by:
- Age (< 30 years vs ≥ 30 years)
- Lesion size (< 2 cm² vs ≥ 2 cm²)
Inclusion criteria:
- Male or female, aged over 18 years.
- Patient who has signed an informed consent form.
- Patient with focal cartilage lesions of the knee, classified as grade 4 on MRI according to the International Cartilage Repair Society classification (exposure of subchondral bone), regardless of their size, and for which surgery is indicated.
- Be affiliated with a social security scheme or a beneficiary of such a scheme
Exclusion criteria:
- Revision knee surgery
- Body Mass Index (BMI) > 27 kg/m2
- Joint space narrowing on standard radiographic examination
- Refusal of consent
- Patient unable to read, write, or understand French
- Vulnerable patient according to Article L1121-6 of the French Public Health Code (CSP)
- Adult patient under guardianship, curatorship, or legal protection
- Patient unable to personally give consent according to Article L.1121-8 of the French Public Health Code (CSP) or an adult protected by law
- Pregnant or breastfeeding woman according to Article L1121-5 of the French Public Health Code (CSP)
- Patient who has already participated in a study within the last 12 months
- Patient already enrolled in another ongoing clinical trial
For patients randomized to the Microfracture arm, the procedure will be as follows: under arthroscopy, the lesion is prepared by debriding it.
Using a specific punch, perforations are made perpendicular to the exposed bone surface.
The technical principles are as follows:
- Perforation depth: approximately 3 to 4 mm, allowing access to the bone marrow,
- Regular spacing between perforations: 3 to 4 mm,
- Preservation of the integrity of the interfracture bone bridges to avoid excessive weakening of the bone endplate.
For patients randomized to the MCI arm, the procedure will be as follows: during surgery, after visualization and debridement of the lesion, cartilage tissue is harvested from a low-weight, and therefore low-stress, area. This cartilage tissue is then fragmented and mixed with PRP (Platelet-Rich Plasma), collected from the patient's blood. Platelets are unique in that they have a high concentration of universal growth factors, enabling them to heal virtually all organic tissues. Adding PRP to the fragmented cartilage tissue promotes cartilage regeneration and the incorporation of the graft into the lesion. To ensure the graft adheres to the bone tissue, it is secured biologically (with thrombin). Post-operative recovery is typical, with a gradual return to walking and other activities.
The participant participation scheme is as follows:
- Baseline: clinical examination + MRI + self-administered questionnaires
- Inclusion and randomization after eligibility verification
- Day 0: surgical intervention according to randomization (MCI vs. microfractures)
- Discharge from hospital: clinical examination + complications
- Post-surgery visit (M3 +/- 1 month): clinical examination + self-administered questionnaires + complications + need for re-surgery
- Post-surgery visit (M9 +/- 1 month): clinical examination + self-administered questionnaires + complications + need for re-surgery
- Post-surgery visit (M24 +/- 1 month): clinical examination + MRI with MOCART score calculation + self-administered questionnaires + complications + need for re-surgery
To demonstrate a difference in filling rate of 30 points (90% in the MCI arm versus 60% in the Microfractures arm) with a standard deviation of 40%, a type I error rate of 5%, and a power of 80%, 28 evaluable subjects per arm are required. To account for unanalyzable data and the potential for patients lost to follow-up, we propose including a total of 80 subjects (40 per arm) in this study.
Tipo di studio
Iscrizione (Stimato)
Fase
- Non applicabile
Contatti e Sedi
Contatto studio
- Nome: Charlotte BOUVET
- Numero di telefono: +33383188340
- Email: charlotte.bouvet@louispasteursante.fr
Luoghi di studio
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Grand Est
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Essey-lès-Nancy, Grand Est, Francia, 54270
- Clinique Louis Pasteur - Louis Pasteur Santé Lorraine
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Contatto:
- Frank WEIN
- Numero di telefono: +33383188340
- Email: frankwein@yahoo.fr
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Investigatore principale:
- Frank WEIN
-
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
Inclusion Criteria:
- Male or female, aged over 18 years.
- Patient who has signed an informed consent form.
- Patient with focal cartilage lesions of the knee, classified as grade 4 on MRI according to the International Cartilage Repair Society classification (exposure of subchondral bone), regardless of size, and for which surgery is indicated.
- Be affiliated with or a beneficiary of a social security scheme.
Exclusion Criteria:
- Revision knee surgery
- Body Mass Index (BMI) > 27 kg/m²
- Joint space narrowing on standard radiographic examination
- Refusal of consent
- Patient unable to read, write, or understand French
- Vulnerable patient according to Article L1121-6 of the French Public Health Code (CSP)
- Adult patient under guardianship, curatorship, or legal protection
- Patient unable to give Personally, their consent according to Article L.1121-8 of the French Public Health Code (CSP) or an adult protected by law
- Pregnant or breastfeeding woman according to Article L1121-5 of the French Public Health Code (CSP)
- Patient who has already participated in a study within the last 12 months
- Patient already enrolled in another ongoing clinical trial
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Doppio
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Comparatore attivo: Arm 1: Microfractures
For patients randomized to the Microfracture arm, the procedure will be as follows: under arthroscopy, the lesion is prepared by debriding it. Using a specific punch, perforations are made perpendicular to the exposed bone surface. The technical principles are as follows:
|
Patients will be randomized in the study to:
Altri nomi:
|
|
Sperimentale: Arm 2: Minced Cartilage Implantation (MCI)
For patients randomized to the MCI arm, the procedure will be as follows: during surgery, after visualization and debridement of the lesion, cartilage tissue is harvested from a low-weight, and therefore low-stress, area.
This cartilage tissue is then fragmented and mixed with PRP (Platelet-Rich Plasma), collected from the patient's blood.
Platelets are unique in their high concentration of universal growth factors, and therefore have the ability to promote the healing of almost all organic tissues.
This addition of PRP to the fragmented cartilage tissue will thus promote cartilage regeneration and the incorporation of the graft within the lesion.
To ensure the graft adheres to the bone tissue, the entire structure is secured biologically (thrombin).
Postoperative recovery is standard, with a gradual resumption of walking and activities.
|
Patients will be randomized in the study to:
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Bone grafting
Lasso di tempo: at 24 months after surgery
|
Bone grafting will be measured by magnetic resonance imaging at 24 months using the MOCART score (Magnetic Resonance Observation of Cartilage Repair Tissue 2.0 Knee Score), which assesses the rate and quality of grafting.
The evaluator will be blinded to the randomization arm.
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at 24 months after surgery
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Functional scores
Lasso di tempo: Baseline, at 3 months, 9 months, 24 months after surgery
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Scores fonctionnels : - Visual Analogic Scale (VAS) |
Baseline, at 3 months, 9 months, 24 months after surgery
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Functional scores
Lasso di tempo: Baseline 3 months, 9 months, 24 months after surgery
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Scores fonctionnels : - Self Knee Value (SKV) |
Baseline 3 months, 9 months, 24 months after surgery
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Functional scores
Lasso di tempo: Baseline 3 months, 9 months, 24 months after surgery
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Functional scores : Knee Injury and Osteoarthritis Outcome Score (KOOS score)
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Baseline 3 months, 9 months, 24 months after surgery
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Functional scores
Lasso di tempo: Baseline 3 months, 9 months and 24 months after surgery
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Tegner Lysholm activity score
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Baseline 3 months, 9 months and 24 months after surgery
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Post-operative complications
Lasso di tempo: Immediately after surgery until max. 96 hours after surgery (corresponding to hospital discharge), 3 months, 9 months, 24 months after surgery
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Post-operative complications of all causes
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Immediately after surgery until max. 96 hours after surgery (corresponding to hospital discharge), 3 months, 9 months, 24 months after surgery
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Re-intervention required
Lasso di tempo: at 3, 9, and 24 months post-surgery
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Re-intervention required
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at 3, 9, and 24 months post-surgery
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Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Frank WEIN, Louis Pasteur Santé Lorraine
Pubblicazioni e link utili
Pubblicazioni generali
- Massen FK, Inauen CR, Harder LP, Runer A, Preiss S, Salzmann GM. One-Step Autologous Minced Cartilage Procedure for the Treatment of Knee Joint Chondral and Osteochondral Lesions: A Series of 27 Patients With 2-Year Follow-up. Orthop J Sports Med. 2019 Jun 13;7(6):2325967119853773. doi: 10.1177/2325967119853773. eCollection 2019 Jun.
- Schreiner MM, Raudner M, Marlovits S, Bohndorf K, Weber M, Zalaudek M, Rohrich S, Szomolanyi P, Filardo G, Windhager R, Trattnig S. The MOCART (Magnetic Resonance Observation of Cartilage Repair Tissue) 2.0 Knee Score and Atlas. Cartilage. 2021 Dec;13(1_suppl):571S-587S. doi: 10.1177/1947603519865308. Epub 2019 Aug 17.
- Wylie JD, Hartley MK, Kapron AL, Aoki SK, Maak TG. Failures and Reoperations After Matrix-Assisted Cartilage Repair of the Knee: A Systematic Review. Arthroscopy. 2016 Feb;32(2):386-92. doi: 10.1016/j.arthro.2015.07.025. Epub 2015 Sep 28.
- Tsuyuguchi Y, Nakasa T, Ishikawa M, Miyaki S, Matsushita R, Kanemitsu M, Adachi N. The Benefit of Minced Cartilage Over Isolated Chondrocytes in Atelocollagen Gel on Chondrocyte Proliferation and Migration. Cartilage. 2021 Jan;12(1):93-101. doi: 10.1177/1947603518805205. Epub 2018 Oct 12.
- Triana J, Hughes AJ, Rao N, Li ZI, Moore MR, Garra S, Strauss EJ, Jazrawi LM, Campbell KA, Gonzalez-Lomas G. Comparable Clinical and Functional Outcomes Between Osteochondral Allograft Transplantation and Autologous Chondrocyte Implantation for Articular Cartilage Lesions in the Patellofemoral Joint at a Mean Follow-Up of 5 Years. Arthroscopy. 2025 Mar;41(3):745-758. doi: 10.1016/j.arthro.2024.05.018. Epub 2024 Jun 4.
- Smith L, Jakubiec A, Biant L, Tawy G. The biomechanical and functional outcomes of autologous chondrocyte implantation for articular cartilage defects of the knee: A systematic review. Knee. 2023 Oct;44:31-42. doi: 10.1016/j.knee.2023.07.004. Epub 2023 Jul 27.
- Schneider S, Ossendorff R, Holz J, Salzmann GM. Arthroscopic Minced Cartilage Implantation (MCI): A Technical Note. Arthrosc Tech. 2020 Dec 19;10(1):e97-e101. doi: 10.1016/j.eats.2020.09.015. eCollection 2021 Jan.
- Saris DB, Vanlauwe J, Victor J, Almqvist KF, Verdonk R, Bellemans J, Luyten FP; TIG/ACT/01/2000&EXT Study Group. Treatment of symptomatic cartilage defects of the knee: characterized chondrocyte implantation results in better clinical outcome at 36 months in a randomized trial compared to microfracture. Am J Sports Med. 2009 Nov;37 Suppl 1:10S-19S. doi: 10.1177/0363546509350694. Epub 2009 Oct 21.
- Salzmann GM, Sah B, Sudkamp NP, Niemeyer P. Reoperative characteristics after microfracture of knee cartilage lesions in 454 patients. Knee Surg Sports Traumatol Arthrosc. 2013 Feb;21(2):365-71. doi: 10.1007/s00167-012-1973-y. Epub 2012 Apr 8.
- Salzmann GM, Ossendorff R, Gilat R, Cole BJ. Autologous Minced Cartilage Implantation for Treatment of Chondral and Osteochondral Lesions in the Knee Joint: An Overview. Cartilage. 2021 Dec;13(1_suppl):1124S-1136S. doi: 10.1177/1947603520942952. Epub 2020 Jul 25.
- Runer A, Ossendorff R, Ottl F, Stadelmann VA, Schneider S, Preiss S, Salzmann GM, Hax J. Autologous minced cartilage repair for chondral and osteochondral lesions of the knee joint demonstrates good postoperative outcomes and low reoperation rates at minimum five-year follow-up. Knee Surg Sports Traumatol Arthrosc. 2023 Nov;31(11):4977-4987. doi: 10.1007/s00167-023-07546-1. Epub 2023 Aug 27.
- Rothdiener M, Uynuk-Ool T, Sudkamp N, Aurich M, Grodzinsky AJ, Kurz B, Rolauffs B. Human osteoarthritic chondrons outnumber patient- and joint-matched chondrocytes in hydrogel culture-Future application in autologous cell-based OA cartilage repair? J Tissue Eng Regen Med. 2018 Feb;12(2):e1206-e1220. doi: 10.1002/term.2516. Epub 2017 Nov 8.
- Moser LB, Fickert S, Pitzek S, Bauer C, Neubauer M, Dammerer D, Zantop T, Landgraeber S, Nehrer S. Minced cartilage for focal cartilage defects-A comprehensive systematic review of surgical techniques in clinical studies, animal studies and basic research studies. Knee Surg Sports Traumatol Arthrosc. 2025 Oct;33(10):3571-3591. doi: 10.1002/ksa.12608. Epub 2025 Mar 7.
- Milano G, Deriu L, Sanna Passino E, Masala G, Manunta A, Postacchini R, Saccomanno MF, Fabbriciani C. Repeated platelet concentrate injections enhance reparative response of microfractures in the treatment of chondral defects of the knee: an experimental study in an animal model. Arthroscopy. 2012 May;28(5):688-701. doi: 10.1016/j.arthro.2011.09.016. Epub 2012 Jan 25.
- Migliorini F, Baroncini A, Bell A, Weber C, Hildebrand F, Maffulli N. Surgical strategies for chondral defects of the patellofemoral joint: a systematic review. J Orthop Surg Res. 2022 Dec 5;17(1):524. doi: 10.1186/s13018-022-03419-4.
- Meyerkort D, Ebert JR, Ackland TR, Robertson WB, Fallon M, Zheng MH, Wood DJ. Matrix-induced autologous chondrocyte implantation (MACI) for chondral defects in the patellofemoral joint. Knee Surg Sports Traumatol Arthrosc. 2014 Oct;22(10):2522-30. doi: 10.1007/s00167-014-3046-x. Epub 2014 May 11.
- Metzler NF, Kondo M, Matsukura K, Ford AJ, Grainger DW, Okano T. Differentiated and Untreated Juvenile Chondrocyte Sheets Regenerate Cartilage Similarly In Vivo. Tissue Eng Part A. 2025 Feb;31(3-4):184-194. doi: 10.1089/ten.tea.2024.0208. Epub 2024 Nov 18.
- Mayr J, Warth F, Oehler N, Majewski M, Lutter C, Blanke F. Treatment of large chondral lesions with an autologous minced cartilage technique and synovial flap leads to superior results compared to matrix associated autologous chondrocyte transplantation technique after 24 months: A controlled clinical trial. Knee Surg Sports Traumatol Arthrosc. 2026 Mar;34(3):815-824. doi: 10.1002/ksa.12708. Epub 2025 May 26.
- Marot V, Justo A, Alshanquiti A, Reina N, Accadbled F, Berard E, Cavaignac E. Simple Knee Value: a simple evaluation correlated to existing knee PROMs. Knee Surg Sports Traumatol Arthrosc. 2021 Jun;29(6):1952-1959. doi: 10.1007/s00167-020-06281-1. Epub 2020 Sep 23.
- Lu Y, Dhanaraj S, Wang Z, Bradley DM, Bowman SM, Cole BJ, Binette F. Minced cartilage without cell culture serves as an effective intraoperative cell source for cartilage repair. J Orthop Res. 2006 Jun;24(6):1261-70. doi: 10.1002/jor.20135.
- Leyh M, Seitz A, Durselen L, Schaumburger J, Ignatius A, Grifka J, Grassel S. Subchondral bone influences chondrogenic differentiation and collagen production of human bone marrow-derived mesenchymal stem cells and articular chondrocytes. Arthritis Res Ther. 2014 Oct 7;16(5):453. doi: 10.1186/s13075-014-0453-9.
- Kraeutler MJ, Belk JW, Purcell JM, McCarty EC. Microfracture Versus Autologous Chondrocyte Implantation for Articular Cartilage Lesions in the Knee: A Systematic Review of 5-Year Outcomes. Am J Sports Med. 2018 Mar;46(4):995-999. doi: 10.1177/0363546517701912. Epub 2017 Apr 19.
- von Keudell A, Han R, Bryant T, Minas T. Autologous Chondrocyte Implantation to Isolated Patella Cartilage Defects. Cartilage. 2017 Apr;8(2):146-154. doi: 10.1177/1947603516654944. Epub 2016 Jul 8.
- Jia Shyan Ong J, Fen Tan S, Kurien T. A systematic review on Autologous Matrix Induced Chondrogenesis (AMIC) for chondral knee defects. Knee. 2024 Dec;51:102-113. doi: 10.1016/j.knee.2024.08.003. Epub 2024 Sep 5.
- Irwin RM, Bonassar LJ, Cohen I, Matuska AM, Commins J, Cole B, Fortier LA. The clot thickens: Autologous and allogeneic fibrin sealants are mechanically equivalent in an ex vivo model of cartilage repair. PLoS One. 2019 Nov 8;14(11):e0224756. doi: 10.1371/journal.pone.0224756. eCollection 2019.
- Hambly K, Griva K. IKDC or KOOS? Which measures symptoms and disabilities most important to postoperative articular cartilage repair patients? Am J Sports Med. 2008 Sep;36(9):1695-704. doi: 10.1177/0363546508317718. Epub 2008 Jun 24.
- Hahn O, Kieb M, Jonitz-Heincke A, Bader R, Peters K, Tischer T. Dose-Dependent Effects of Platelet-Rich Plasma Powder on Chondrocytes In Vitro. Am J Sports Med. 2020 Jun;48(7):1727-1734. doi: 10.1177/0363546520911035. Epub 2020 Apr 13.
- Goller SS, Heuck A, Erber B, Fink N, Ruckel J, Niethammer TR, Muller PE, Ricke J, Baur-Melnyk A. Magnetic resonance observation of cartilage repair tissue (MOCART) 2.0 for the evaluation of retropatellar autologous chondrocyte transplantation and correlation to clinical outcome. Knee. 2022 Jan;34:42-54. doi: 10.1016/j.knee.2021.11.003. Epub 2021 Dec 6.
- Gebhardt S, Zimmerer A, Balcarek P, Wassilew GI, Schoon J. The Influence of Arthroscopic Shaver Mincing and Platelet-Rich Plasma on Chondrocytes of Intraoperatively Harvested Human Cartilage. Am J Sports Med. 2023 Aug;51(10):2679-2687. doi: 10.1177/03635465231181633. Epub 2023 Jul 14.
- Frodl A, Siegel M, Fuchs A, Wagner FC, Schmal H, Izadpanah K, Yilmaz T. Minced Cartilage Is a One-Step Cartilage Repair Procedure for Small Defects in the Knee-A Systematic-Review and Meta-Analysis. J Pers Med. 2022 Nov 18;12(11):1923. doi: 10.3390/jpm12111923.
- Farr J, Tabet SK, Margerrison E, Cole BJ. Clinical, Radiographic, and Histological Outcomes After Cartilage Repair With Particulated Juvenile Articular Cartilage: A 2-Year Prospective Study. Am J Sports Med. 2014 Jun;42(6):1417-25. doi: 10.1177/0363546514528671. Epub 2014 Apr 9.
- Ebert JR, Klinken S, Fallon M, Wood DJ, Janes GC. Clinical and Radiological Outcomes at >/=10-Year Follow-up After Matrix-induced Autologous Chondrocyte Implantation in the Patellofemoral Joint. Am J Sports Med. 2024 Aug;52(10):2532-2540. doi: 10.1177/03635465241262337. Epub 2024 Aug 5.
- Dasari SP, Jawanda H, Mameri ES, Fortier LM, Polce EM, Kerzner B, Gursoy S, Hevesi M, Khan ZA, Jackson GR, Cole BJ, Yanke AB, Verma NN, Chahla J. Single-stage autologous cartilage repair results in positive patient-reported outcomes for chondral lesions of the knee: a systematic review. J ISAKOS. 2023 Oct;8(5):372-380. doi: 10.1016/j.jisako.2023.05.003. Epub 2023 May 24.
- Cotter EJ, Sachs JP, Cole BJ. Editorial Commentary: Autologous Minced Repair of Knee Cartilage Is Safely and Effectively Performed Using Arthroscopic Techniques. Arthroscopy. 2025 Mar;41(3):771-773. doi: 10.1016/j.arthro.2024.06.025. Epub 2024 Jun 21.
- Cole BJ, Farr J, Winalski CS, Hosea T, Richmond J, Mandelbaum B, De Deyne PG. Outcomes after a single-stage procedure for cell-based cartilage repair: a prospective clinical safety trial with 2-year follow-up. Am J Sports Med. 2011 Jun;39(6):1170-9. doi: 10.1177/0363546511399382. Epub 2011 Apr 1.
- Christensen BB, Olesen ML, Lind M, Foldager CB. Autologous Cartilage Chip Transplantation Improves Repair Tissue Composition Compared With Marrow Stimulation. Am J Sports Med. 2017 Jun;45(7):1490-1496. doi: 10.1177/0363546517694617. Epub 2017 Mar 20.
- Christensen BB, Foldager CB, Jensen J, Lind M. Autologous Dual-Tissue Transplantation for Osteochondral Repair: Early Clinical and Radiological Results. Cartilage. 2015 Jul;6(3):166-73. doi: 10.1177/1947603515580983.
- Chahal J, Lansdown DA, Davey A, Davis AM, Cole BJ. The Clinically Important Difference and Patient Acceptable Symptomatic State for Commonly Used Patient-Reported Outcomes After Knee Cartilage Repair. Am J Sports Med. 2021 Jan;49(1):193-199. doi: 10.1177/0363546520969883. Epub 2020 Nov 23.
- Bos PK, Kops N, Verhaar JA, van Osch GJ. Cellular origin of neocartilage formed at wound edges of articular cartilage in a tissue culture experiment. Osteoarthritis Cartilage. 2008 Feb;16(2):204-11. doi: 10.1016/j.joca.2007.06.007. Epub 2007 Jul 27.
- Bonasia DE, Marmotti A, Mattia S, Cosentino A, Spolaore S, Governale G, Castoldi F, Rossi R. The Degree of Chondral Fragmentation Affects Extracellular Matrix Production in Cartilage Autograft Implantation: An In Vitro Study. Arthroscopy. 2015 Dec;31(12):2335-41. doi: 10.1016/j.arthro.2015.06.025. Epub 2015 Aug 28.
- Basad E, Wissing FR, Fehrenbach P, Rickert M, Steinmeyer J, Ishaque B. Matrix-induced autologous chondrocyte implantation (MACI) in the knee: clinical outcomes and challenges. Knee Surg Sports Traumatol Arthrosc. 2015 Dec;23(12):3729-35. doi: 10.1007/s00167-014-3295-8. Epub 2014 Sep 14.
- Albrecht F, Roessner A, Zimmermann E. Closure of osteochondral lesions using chondral fragments and fibrin adhesive. Arch Orthop Trauma Surg (1978). 1983;101(3):213-7. doi: 10.1007/BF00436773.
- Abraamyan T, Johnson AJ, Wiedrick J, Crawford DC. Marrow Stimulation Has Relatively Inferior Patient-Reported Outcomes in Cartilage Restoration Surgery of the Knee: A Systematic Review and Meta-analysis of Randomized Controlled Trials. Am J Sports Med. 2022 Mar;50(3):858-866. doi: 10.1177/03635465211003595. Epub 2021 Apr 23.
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