Recruiting

Observational Study

Sponsor:

Hyalex Orthopaedics, Inc.

Code:

NCT06368700

Conditions

Damaged Chondral or Osteochondral Area

Eligibility Criteria

Sex: All

Age: 22 - 70

Healthy Volunteers: Not accepted

Interventions

Hyalex Knee Cartilage System

Study Details

Brief summary:

A multicenter, open-label, single-arm, pivotal study to evaluate the safety and effectiveness of the HYALEX Freestyle Resurfacing System for replacement of loss of articular cartilage and bone of the knee femoral condyles in symptomatic patients who require surgical treatment, will be enrolled in the study and undergo implantation of the HYALEX Freestyle Resurfacing Implant.

Conditions

Damaged Chondral or Osteochondral Area

Study ID

NCT06368700

Start date

Apr 4, 2024

Status verified date

Apr, 2026

Completion date

Dec, 2028

Anticipated

Primary completion date

Dec, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 22 - 70

Healthy Volunteers: Not accepted

Inclusion Criteria (Phase 1):

1. 22-70 years.
2. Body Mass Index (BMI) ≤ 40.
3. Up to two treatable joint surface lesion, ICRS Grade 3 or 4, located on the medial and/or lateral femoral condyle.
4. Up to 2 implants (one implant per condyle) to treat up to 2 individual symptomatic lesions with a total summative area up to 4.52cm2 / condyle.
5. Knee Injury and Osteoarthritis Outcome Score (KOOS) pain subscale score between 20 and 65.
6. Ligamentously stable knee.
7. Failure of non-operative treatment (e.g., physical therapy, physician-directed at home exercise program, intra-articular injections, bracing) for at least 4 months prior to consideration for participation in the study.

Exclusion Criteria:

HYALEX Implant, Surgical Technique, and Lesion Site Exclusions:

1. Known allergy to polyurethanes, bone cement, acrylic, or titanium.
2. Lack of 2mm of cartilage (ICRS Grade 0 to 2) and 2mm of vital bone wall on all sides of the implant site.
3. Osteochondral defect affecting subchondral bone more than 11mm in depth from adjacent non-defect articular surface.
4. Bipolar cartilage lesions involving patellar or tibial lesions ICRS Grade 3 - 4 opposite the lesion intended for treatment.
5. Insufficient bone stock or bone density determined intra-operatively preventing implant press fit.

Patient Orthopaedic Health Exclusions:

1. Kellgren and Lawrence (KL) grade 3 or 4 on standing radiographs.
2. Hip-knee-ankle (HKA) angle of greater than +/- 8 degrees (varus or valgus malalignment > 8 degrees) on standing X-ray.
3. Lack of normally functioning contralateral knee that restricts activity.
4. Recent Osteochondritis Dissecans within 1 year.
5. Diagnosis of a concomitant knee injury which the investigator believes may interfere with study participation or confound effectiveness assessment.
6. Untreated ACL and/or PCL deficiency or complex ligamentous instability of the study knee according to IKDC Grade C (abnormal) or D (severely abnormal).

Previous Surgery and Intervention Exclusions:

1. Previous surgical cartilage treatment in the index knee within the last 6 months
2. Previous intra-articular injections, including HA and steroids, within the last 3 months prior to the date of surgery.

Patient Overall Health and Health History Exclusions:

1. Any known history of inflammatory arthropathy or untreated or uncontrolled crystal-deposition arthropathy.
2. Current cigarette smoker or user of other nicotine products.
3. Known Type 1 or Type 2 insulin-dependent diabetes mellitus.
4. Currently undergoing immunosuppressive therapy or long-term steroid use (corticosteroid, excluding inhalers) or within 3 months prior to surgery.

Study Design

Enrollment

85 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: HYALEX Freestyle Resurfacing System

Implantation of the HYALEX Implant

Interventions

Hyalex Knee Cartilage System

Surgical implantation of the Hyalex Knee Cartilage System

Primary outcome measure

  • Composite Primary Endpoint [ Time Frame: 12 months ]
  • Change in the Knee Injury & Osteoarthritis Outcome Score (KOOS) at 12 months. [ Time Frame: 12 months ]

Central Contacts and Locations

Central contacts

Locations

Horizon Clinical Research

Recruiting

La Mesa, California, United States, 91942

Contacts

Principal Investigator:

Scott Hacker, M.D.

Ochsner Sports Medicine Institute

Recruiting

New Orleans, Louisiana, United States, 70121

Contacts

Principal Investigator:

Brian Godshaw, M.D.

Hospital for Special Surgery

Recruiting

New York, New York, United States, 10021

Contacts

Principal Investigator:

Sabrina Strickland, M.D.

Oregon Health & Science University

Recruiting

Portland, Oregon, United States, 97239

Contacts

Principal Investigator:

Dennis Crawford, M.D.

More Information

Sponsor

Hyalex Orthopaedics, Inc.

Last update posted

Apr 16, 2026

Last verified

Apr, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Hyalex Orthopaedics, Inc. on 2026-04-16.