Chondro-Gide® Bilayer Collagen Membrane in Knee Cartilage Defect Repair
- Conditions
- Cartilage Defects
- Interventions
- Procedure: MicrofractureDevice: Chondro-Gide bilayer collagen membrane
- Registration Number
- NCT05785949
- Lead Sponsor
- Geistlich Pharma AG
- Brief Summary
A prospective, multicenter, randomized, parallel controlled study evaluating the safety and efficacy of Chondro-Gide® bilayer collagen membrane in knee cartilage defect repair. The objective of this clinical trial is to evaluate the efficacy and safety of Chondro-Gide® bilayer collagen membrane in knee cartilage defect repair
- Detailed Description
This is a prospective, multicenter, randomized, parallel controlled and superiority clinical trial. It is planned to be carried out in hospitals with qualifications as a national-level clinical trial institution. Subjects who have signed the ICF, meet all inclusion criteria and do not meet any exclusion criteria will be included in this study. Subjects included will be randomly assigned into the experimental group and the control group at a ratio of 1:1. Those in the control group will receive microfracture, and those in the experimental group will receive microfracture plus Chondro-Gide® bilayer collagen membrane. The primary efficacy evaluation indicator of this clinical study is the MOCART score at 24 months postoperative. The secondary efficacy evaluation indicators are IKDC score (before operation, 3, 6, 12 and 24 months postoperative), MOCART score (6 and 12 months postoperative), hyaline cartilage production (T2 mapping ratio) (12 and 24 months postoperative), Lysholm score (before operation, 3, 6, 12 and 24 months postoperative), and device performance evaluation of the investigational product. Safety evaluation indicators include adverse events (or serious adverse events), device-related adverse events (or serious adverse events), device deficiencies and laboratory examination.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 140
- Male or female patients aged 18-55 years (including 18 years and 55 years);
- Localized cartilage defects on knee joint, the size of the defect after debridement is 2.0 squared cm - 8.0 squared cm (including 2.0 squared cm and 8.0 squared cm), which was classified by the International Cartilage Repair Society (ICRS) as grade Ⅲ or grade IV;
- The subjects voluntarily consent to participate in this trial and sign the informed consent form (ICF).
- Body mass index (BMI) ≥ 30 kg/meter squared (BMI = weight divided by height squared);
- Unilateral knee cartilage defect with the ICRS classification of grade III or grade IV, and with three or more defects;
- Patients with abnormal lower limb mechanical axis requiring correction, except those that could be corrected during the treatment of cartilage injury;
- Varus or valgus of lower limb axis > 5°, requiring osteotomy for correction;
- Patients with multiple ligament injury or total meniscectomy;
- Those who are known to be allergic to porcine-derived materials or collagen, or refuse to use porcine-derived medical products;
- Those with severe arthroclisis or arthrofibrosis;
- Those who have received open knee surgery in the past 6 months;
- Those who have received microfracture, mosaicplasty or autologous cartilage implantation in the past 3 months;
- Those who have serious primary cardiovascular diseases, lung diseases, endocrine and metabolic diseases (severe diabetes, severe osteoporosis) or serious diseases affecting their survival, and are considered unsuitable for inclusion by the investigators;
- Pregnant and lactating women, or those who plan to conceive during the trial, and those who have positive blood/urine pregnancy test results before the trial;
- Patients with knee infection；
- Those with connective tissue diseases;
- Those with nervous system diseases or muscle degeneration;
- Patients who participated in drug clinical trials within 3 months prior to the enrollment or patients who participated in any other device clinical trials within 1 months prior to the enrollment;
- Other circumstances which are considered by the investigator not suitable for enrollment in this study.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Microfracture Microfracture Microfracture Microfracture + Chondro-Gide® Microfracture Microfracture + Chondro-Gide® bilayer collagen membrane Microfracture + Chondro-Gide® Chondro-Gide bilayer collagen membrane Microfracture + Chondro-Gide® bilayer collagen membrane
- Primary Outcome Measures
Name Time Method Magnetic Resonance Observation of Cartilage Repair Tissue (MOCART) 24 months postoperative Cartilage repair is evaluated by MOCART score from nine aspects, such as degree of defect repair and filling of the defect, integration to border zone, surface of repair tissue, structure of the repair tissue, adhesions and subchondral lamina.
- Secondary Outcome Measures
Name Time Method International Knee Documentation Committee (IKDC) score before operation and at 3, 6, 12 and 24 months postoperative The therapeutic effect for subjects is evaluated based on the difference between IKDC score at the different timepoints. The score ranges from 0 - 87 points, where higher scores mean a better outcome.
Safety indicators; adverse events and device deficiencies through study completion, an average of 2 years 1. Incidence (%) and number of (serious) adverse events, and those of device-related (serious) adverse events;
2. Incidence (%) and number of device deficiencies;Magnetic Resonance Observation of Cartilage Repair Tissue (MOCART) 6 and 12 months postoperative Cartilage repair is evaluated by MOCART score from nine aspects, such as degree of defect repair and filling of the defect, integration to border zone, surface of repair tissue, structure of the repair tissue, adhesions and subchondral lamina. The Score ranges from 0 - 100, where higher scores mean a better outcome.
Hyaline cartilage production (T2 mapping ratio) 12 and 24 months postoperative Please refer to YY/T 1636-2018 Tissue engineering medical device products-In vivo evaluation of knee cartilage implanted tissue using MRI technique for the specific operation, measurement and evaluation method of T2 mapping technology of MRI.
Device performance evaluation questionnaire perioperative (after surgical intervention), on the day of surgery The investigator evaluates the performance of the device based on a questionnaire. The evaluation criteria are as follows. There are three answer options to every question:
1. Is the product operation convenient?
2. Is the product easy to trim?
3. Is the product easy to fix?
4. Is the product compliant after being fixed?Safety indicators; Laboratory examination before operation, 7 days and 6 months postoperative Determination of clinical significance of laboratory examination: 1) normal; 2) abnormal but without clinical significance; 3) abnormal with clinical significance; 4) not examined. If the clinical significance is judged as 3) abnormal with clinical significance, the abnormality is explained, followed up, and reexamined until normal or reaching baseline level or stable.
Lysholm score before operation and at 3, 6, 12 and 24 months postoperative The Lysholm score is assessing patient's knee specific symptoms. The total Lysholm score is 100 (0: worst, 100: best).
Trial Locations
- Locations (10)
The Third Affiliated Hospital of Southern Medical University
🇨🇳Guangzhou, China
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
🇨🇳Nanjing, China
The Second Hospital of Jilin University
🇨🇳Changchun, China
The First Affiliated Hospital of Jinan University
🇨🇳Guangzhou, China
The First Affiliated Hospital Of Nanchang University
🇨🇳Nanchang, China
The second affiliated hospital of Zhejiang University School of Medicine
🇨🇳Hanzhou, China
Sino-Japanese Friendship Hospital
🇨🇳Peking, China
Inner Mongolia People's Hospital
🇨🇳Hohhot, China
The First Affiliated Hospital of Kunming Medical University
🇨🇳Kunming, China
Peking University Third Hospital
🇨🇳Peking, China