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Effect of Autologous Ear Cartilage Micrografting in Knee Osteoarthritis (EAR2KNEE)

2026年8月4日 更新者:Regenera Activa Worldwide S.L.

Effect of Autologous Cartilage Micrografting in Knee Cartilage Disease

The goal of this clinical trial is to learn if a single injection of autologous cartilage micrografts suspension, obtained through processing with a specialized technology patient's own small piece of ear cartilage, can improve knee osteoarthritis in adult men and women aged 18-75 with confirmed moderate knee osteoarthritis. The main questions it aims to answer are:

  • Does a single intra-articular injection of autologous ear-cartilage micrografts improve patients' clinical symptoms and knee function over 12 months?
  • What percentage of patients experience improvement in their complaints following treatment?
  • Do MRI scans show measurable improvement in knee cartilage condition 6 months after treatment?
  • Do inflammatory cytokine levels (IL-1β, IL-1α, IL-6, TNF-α) in joint fluid and cartilage tissue correlate with treatment response?

調査の概要

詳細な説明

Background and Rationale Knee osteoarthritis is among the most common orthopedic conditions, affecting an estimated 10-12% of the population. Left untreated, it tends to progress, leading to worsening degenerative joint changes and functional loss. Treatment remains difficult because articular cartilage has very limited natural regenerative capacity. Currently used approaches - arthroscopic debridement, radiofrequency chondroplasty, and hyaluronic acid injection - have inconsistent or unsatisfactory efficacy.

This study reproduces a previously published treatment procedure using autologous cartilage micrografts sourced from the patient's own auricular (ear) cartilage, rather than from the knee joint itself or from cultured chondrocytes. Ear cartilage was selected as the donor tissue for three reasons: (1) elastic auricular cartilage has physical and biological properties closer to the hyaline cartilage found in the knee joint than other readily accessible cartilage sources; (2) the sampling procedure is simple and minimally invasive compared to harvesting from a weight-bearing joint; and (3) the perichondrial tissue surrounding ear cartilage contains a high density of chondroprogenitor cells responsible for regenerative processes.

Study Design The research has two components conducted on the same patient cohort: a clinical component evaluating the treatment's effect on patients' symptoms and joint imaging, and a laboratory component measuring inflammatory cytokine concentrations in tissue and joint fluid samples collected during the same procedure. This is a single-arm interventional study; there is no placebo or active comparator, and no randomization or blinding, since every enrolled participant receives the identical intervention on one knee affected by osteoarthritis.

Procedure

Each participant is treated on a single, affected knee. The procedure begins with drainage and storage of synovial fluid from the affected knee, for two reasons: synovial fluid in patients with knee osteoarthritis is expected to carry a high concentration of inflammatory cytokines that may impede improvement or contribute to discomfort, and removing it prevents dilution of the cartilage micrograft suspension subsequently injected.

Cartilage tissue is then harvested from the patient's own ear using a 2,5 mm dermatological punch - 3 biopsies maintaining a sterile field, under local anesthesia with lidocaine to ensure the harvesting is painless. The biopsies are placed inside a sterile medical disposable device class IIa (Rigeneracons RS) and 4 milliliters of sterile physiological saline are added to the harvested tissue. The device mechanically mills the cartilage into 80 microns micrografts thanks to Rigenera Technology - Mytocel MSK. This suspension is drawn into a syringe and delivered via a single anterolateral-approach injection directly into the synovial space of the osteoarthritic knee. The full procedure takes approximately 30 minutes and is considered as minimally invasive.

Cytokine Sub-Study For the laboratory component, a small aliquot (100 microliters) of the harvested ear cartilage suspension is frozen and stored (initially at -20°C, then at -80°C) at the time of tissue collection, before the remainder is injected. The synovial fluid drained from the knee prior to injection is handled and stored the same way. Concentrations of four cytokines associated with inflammation - IL-1β, IL-1α, IL-6, and TNF-α - are measured in both sample types. These measurements generate an individual inflammatory profile for each participant at baseline, which is then considered when interpreting each patient's clinical outcomes, on the hypothesis that a patient's baseline inflammatory state may influence how well they respond to treatment.

Basis for Expected Results A prior study using the same procedure and the same medical device reported successful interventions in all cases, with no wound-healing disorder or infection, no aesthetic deficit at the ear donor site, universal patient-reported pain relief and return to daily activity, significant improvement on clinical questionnaires, and an increase in lateral femoral condyle thickness on MRI performed at three years post-intervention. This study is designed to evaluate whether comparable outcomes are observed in the current knee osteoarthritis patient cohort.

Data Handling Data collection and processing are conducted solely for research purposes. Samples are processed anonymously using a code number system. A single technical record is maintained per participant, documenting all data, facts, and events relevant to or potentially influencing the study outcome. Code sheets linking code numbers to personal identifying data are kept in a locked file and separated from experimental data. Data are handled confidentially and are not shared with third parties. After processing, participant data are aggregated so that individuals cannot be identified from published results.

Statistical Analysis Outcome measures (KOOS subscales, including Pain and Symptoms/Stiffness; and Visual Analog Scale pain scores for current, worst, and best pain) were analyzed using repeated-measures ANOVA across five assessment timepoints (Baseline, Week 1, Month 3, Month 6, and Year 1) to test for an overall effect of visit/time. Mauchly's test of sphericity was applied to each outcome; where sphericity was violated, the Greenhouse-Geisser correction was used to adjust the degrees of freedom and significance values.

Where the overall visit effect was significant, simple contrasts compared each follow-up timepoint (Week 1, Month 3, Month 6, Year 1) against Baseline, with effect sizes reported as Cohen's d for each pairwise comparison. Descriptive statistics (mean, standard deviation, standard error, coefficient of variation) were reported for each timepoint.

研究の種類

介入

入学 (実際)

33

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  • Diagnosed knee OA L-K grade II-III
  • Symptomatic knee OA (with pain)
  • Reduced mobility

Exclusion Criteria:

  • Knee OA L-K grade IV
  • Systemic Joint Disease (e.g. rheumatoid arthritis)
  • Active autoimmune disease
  • Active Oncologic process
  • If other orthobiologic treatments administered in the last 3 months

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
他の:Intervention Group
Autologous Cartilage Micrografting is performed to all subjects with moderate knee osteoarthritis
Autologous Ear Cartilage micrografting using Rigenera Technology - Mytocel MSK. A 2.5 mm punch biopsy of the patient's own auricular ear cartilage is harvested under local anesthesia. The tissue is mechanically disaggregated within the device after addition of 4mL sterile physiological saline, yielding a micrograft suspension containing autologous cartilage progenitor cells - without cell culture, expansion, or enzymatic digestion. The micrograft suspension is then delivered as a single intra-articular injection. The procedure is performed once per patient, on one knee, in a single outpatient session lasting approximately 30 minutes.
他の名前:
  • Mytocel MSK
  • Autologous Micrografting
  • Rigenera Technology

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Change in Knee Osteoarthritis Outcome Score (KOOS)
時間枠:Baseline, 1 week, 3 months, 6 months, 12 months, and 24 months
Change from baseline in KOOS subscale scores (including Pain and Symptoms/Stiffness), scored 0-100 with higher scores indicating better knee-related quality of life and function. Assessed via repeated-measures analysis across follow-up visits relative to baseline
Baseline, 1 week, 3 months, 6 months, 12 months, and 24 months

二次結果の測定

結果測定
メジャーの説明
時間枠
Change in knee cartilage thickness on MRI
時間枠:Baseline, 6 months
MRI-assessed change in knee joint cartilage structure (e.g., lateral femoral condyle thickness) following treatment.
Baseline, 6 months
Baseline synovial fluid and cartilage tissue cytokine concentrations
時間枠:Time of the procedure
Concentrations of IL-1β, IL-1α, IL-6, and TNF-α measured in synovial fluid and harvested ear cartilage tissue, used to generate an inflammatory profile for each participant at baseline.
Time of the procedure

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:Zsombor Lacza, Dr、Prof. of Sports Science at University of Sports Science, Budapest, Hungary

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2023年5月22日

一次修了 (実際)

2025年12月21日

研究の完了 (推定)

2027年12月21日

試験登録日

最初に提出

2026年8月4日

QC基準を満たした最初の提出物

2026年8月4日

最初の投稿 (実際)

2026年8月10日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月10日

QC基準を満たした最後の更新が送信されました

2026年8月4日

最終確認日

2026年8月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • MYTOCEL-KNEE-OA-052023
  • Official Research Registration (レジストリ識別子:863)
  • ref. BM/1298-3/2024 (その他の識別子:ETT TEKUB)
  • OGYÉI/67359-9/2023 (その他の識別子:OGEIY Hungary)

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

未定

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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