We're building a better ClinicalTrials.gov. Check it out and tell us what you think!
ClinicalTrials.gov Menu

Evaluation of the Agili-C Biphasic Implant in the Knee Joint

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT01471236
Recruitment Status : Completed
First Posted : November 15, 2011
Last Update Posted : August 26, 2021
Information provided by (Responsible Party):
Cartiheal (2009) Ltd

Brief Summary:
The purpose of this study is to determine the performance of the Agili-C implants. The study hypothesis is that Agili-C implants are effective in the treatment of focal cartilage and cartilage-bone joint surface defects.

Condition or disease Intervention/treatment Phase
Cartilage Diseases Osteochondritis Dissecans Device: Agili-C Bi-phasic Implant Procedure: mini-arthrotomy Not Applicable

Detailed Description:
Agili-C implant is a bi-phasic, porous resorbable tissue regeneration scaffold for the treatment of focal articular cartilage and for osteochondral defects. Up to 50 patients are to be included in the study. Patients suffering from isolated, single and focal cartilage or osteochondral defect at the knee joint are considered for study inclusion.

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 65 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Evaluation of the Agili-C Bi-phasic Implant Performances in the Repair of Cartilage and Osteochondral Defects
Study Start Date : June 2011
Actual Primary Completion Date : November 19, 2018
Actual Study Completion Date : November 19, 2018

Arm Intervention/treatment
Experimental: Agili-c bi-phasic implant
Device: Agili-C Bi-phasic Implant

The implantation site should be created in perpendicular manner to the articular cartilage. The surrounding tissue will be cleaned and scraped to prepare a clean site. The implant will be placed in the correct orientation (drilled channels pointing towards the joint side and chamfer towards the bone).

The implant will be inserted gently in a pressed fit manner.

Other Name: Agili-C implant

Procedure: mini-arthrotomy

The procedure will be conducted according to hospital practice. The implants will be positioned via open incision, depending on lesion location, and Investigator's final decision. Related treatments during the procedure should be recorded.

Device positioning details medications and adverse events during the procedure will be recorded. MOCART (off-site), X-ray evaluation (off-site), ICRS Cartilage injury mapping system, Articular cartilage injury Classification and the Osteochondritis Dissecans classification will be recorded.

Primary Outcome Measures :
  1. improvement in KOOS pain subscales [ Time Frame: 24 months ]
    The primary efficacy endpoint for this trial will be the change from baseline up to 24 months visit in pain score as measured by the KOOS pain subscale

Secondary Outcome Measures :
  1. KOOS total score [ Time Frame: 24 months ]
    • Change from baseline to 3, 6, 9, 12, 18 and 24 months visits as measured by the KOOS total score and subscales.
    • Change from baseline to 18 and 24 months visit in IKDC current health assessment.
    • Change from baseline to 3, 6, 12, 18 and 24 months visit in Lysholm with Tegner knee score.
    • Change from baseline to 3, 6, 12 , 18 and 24 months visit in IKDC knee examination form 2000
    • Change from baseline to 3, 6, 12 , 18 and 24 months visit in IKDC subjective knee evaluation
    • Change in MOCART scoring as measured at 3, 6, 12 , 18 and 24 months visit

Other Outcome Measures:
  1. number of SAE [ Time Frame: 24 months ]
    Complications and adverse events, device-related or not, will be evaluated over the course of the clinical trial, including subsequent surgical interventions

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Layout table for eligibility information
Ages Eligible for Study:   18 Years to 55 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria

  1. 18 to 55 years
  2. Symptomatic, single, focal, full or near full-thickness (ICRS cartilage defect description grades 3 and 4) chondral or osteochondral isolated lesion of the femoral condyle, trochlea or the tibial plateau

    • Defect area is less than 2 cm² after debridement. The defect is completely surrounded on all sides by healthy cartilage.
    • Osteochondral defect ICRS Cartilage defect description type 1, 2, 3, 4A. Maximal defect depth should be up to 3 millimeters.
  3. Primary or secondary articular cartilage repair.
  4. Knee is stable or can be stabilized as a concomitant procedure.
  5. Must be physically and mentally willing and able to comply with post-operative rehabilitation and routinely schedule clinical and radiographic visits.
  6. Signed informed consent.
  7. Any misalignments should be fully corrected at the end of the operative procedure.

Exclusion Criteria

  1. Uncorrected axial misalignments >5° that cannot be corrected.
  2. Patellar cartilage defects or pathology.
  3. Meniscal resection of more than 50%, either in a previous procedure or concomitant with articular cartilage repair.
  4. Any tumor of the ipsilateral knee, any concurrent malignant tumor or any metastatic tumor in the past or in the present.
  5. Active acute or chronic infection of the treated knee.
  6. Inflammatory arthropathy or crystal-deposition arthropathy.
  7. Systemic cartilage and/or bone disorder; This implants integration is dependent on surrounding live bleeding bone; therefore it must not be implanted within sequestrated or necrotic bone.
  8. Bony defect depth over 3 millimeters.
  9. Body mass index >35.
  10. Asymptomatic articular cartilage defects.
  11. Bipolar articular cartilage defects.
  12. Osteoarthritis of the operated knee.
  13. Oral medications such as systemic corticosteroid therapy taken less than one year prior to surgery or chemotherapy.

    • Previous operative treatment of Arthroscopic marrow stimulation technique or cell therapy operated within the last 6 months
    • Any previous operation of cartilage treatment within the last 6 months
  14. Patients who are sensitive to materials containing calcium carbonate or hyaluronate
  15. Pregnant women, women who plan to become pregnant and breastfeeding women.
  16. Evidence of any significant systemic disease (such as but not limited to HIV infection, hepatitis infection or HTLV infection), known coagulopathies, severe vascular or neurological disease or acute injury that might compromise the patient's welfare.
  17. Substance abuse or alcohol abuse.
  18. Participation in another clinical trials in parallel to this study.
  19. Type I diabetes.
  20. Unable to undergo MRI or X-ray.
  21. Any reasons making the patient a poor candidate in the opinion of the investigator.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01471236

Layout table for location information
Clinical Hospital ''Sveti Duh''
Zagreb, Croatia
Fakultní nemocnice Brno
Brno, Czechia
Uzsoki Street Hospital
Budapest, Hungary
Rizzoli Orthopaedic Institute
Bologna, Italy
Avimed Hospital
Katowice, Poland
County Hospital of Timisoara,
Timisoara, Romania
Institut Za Ortopediju "Banjica"
Belgrade, Serbia
Clinical center of Vojvodina
Novi Sad, Serbia
University Medical Centre, Ljubljana
Ljubljana, Slovenia
Sponsors and Collaborators
Cartiheal (2009) Ltd
Layout table for investigator information
Principal Investigator: Elizaveta Kon, MD
Layout table for additonal information
Responsible Party: Cartiheal (2009) Ltd
ClinicalTrials.gov Identifier: NCT01471236    
Other Study ID Numbers: CLN0002
First Posted: November 15, 2011    Key Record Dates
Last Update Posted: August 26, 2021
Last Verified: February 2020
Keywords provided by Cartiheal (2009) Ltd:
Additional relevant MeSH terms:
Layout table for MeSH terms
Osteochondritis Dissecans
Cartilage Diseases
Bone Diseases
Musculoskeletal Diseases
Connective Tissue Diseases