Skip to content
Bored Studies
Recruiting

The HYALEX Pivotal Study

Hyalex Orthopaedics, Inc. · NCT06368700

View Study & Apply (opens in a new tab)

Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 22–70 · All sexes
Healthy volunteers
Not accepted (a condition is required)
Study type
Interventional · Not applicable
Target enrollment
85
US sites recruiting
4
Study start
April 4, 2024
Record last updated
October 7, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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.

Being studied: Hyalex Knee Cartilage System

Conditions: Damaged Chondral or Osteochondral Area

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria (Phase 1):

  • 22-70 years.
  • Body Mass Index (BMI) ≤ 40.
  • Up to two treatable joint surface lesion, ICRS Grade 3 or 4, located on the medial and/or lateral femoral condyle.
  • 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.
  • Knee Injury and Osteoarthritis Outcome Score (KOOS) pain subscale score between 20 and 65.
  • Ligamentously stable knee.
  • 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:

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

Patient Orthopaedic Health Exclusions

  • Kellgren and Lawrence (KL) grade 3 or 4 on standing radiographs.
  • Hip-knee-ankle (HKA) angle of greater than +/- 8 degrees (varus or valgus malalignment > 8 degrees) on standing X-ray.
  • Lack of normally functioning contralateral knee that restricts activity.
  • Recent Osteochondritis Dissecans within 1 year.
  • Diagnosis of a concomitant knee injury which the investigator believes may interfere with study participation or confound effectiveness assessment.
  • 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:

  • Previous surgical cartilage treatment in the index knee within the last 6 months
  • 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:

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

Recruiting US locations

  • Horizon Clinical Research

    La Mesa, CA 91942

    Site contact: Dino Subasic · (619) 456-6012 · dino@horizontrials.com

  • Ochsner Sports Medicine Institute

    New Orleans, LA 70121

    Site contact: Joseph Laurent · (504) 842-0263 · joseph.laurent@ochsner.org

  • The Ohio State University Wexner Medical Center - Sports Medicine

    Columbus, OH 43202

    Site contact: Jenna DeFranco · 614-293-2761 · jenna.defranco@osumc.edu

  • Oregon Health & Science University

    Portland, OR 97239

    Site contact: Jessica Ballin · 503-418-9580 · ballin@ohsu.edu

Study contacts (from the official record)

  • Chris Cain · 408-439-5154 · chris.cain@hyalex.com
The HYALEX Pivotal Study (NCT06368700) | Bored Studies