Actively Recruiting

Phase Not Applicable
Age: 22Years - 60Years
All Genders
NCT07249489

Nanochon Chondrograft First in Human (FIH) Early Feasibility Study (EFS) - Canada

Led by Nanochon, Inc. · Updated on 2026-04-22

10

Participants Needed

2

Research Sites

69 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this First in Human study is to learn if the Nanochon Chondrograft Implant is a safe primary surgical treatment for participants with cartilage lesions in the knee. This study will include males and females between the ages of 22 and 60.

CONDITIONS

Official Title

Nanochon Chondrograft First in Human (FIH) Early Feasibility Study (EFS) - Canada

Who Can Participate

Age: 22Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female aged 22 to 60 years
  • MRI knee evaluation completed within 6 months prior to enrollment
  • Able to read and speak English
  • Voluntarily signed informed consent form
Not Eligible

You will not qualify if you...

  • Known systemic cartilage or bone disorders such as osteoporosis, chondrodysplasia, or osteogenesis imperfecta
  • Requires bilateral knee surgery
  • Pregnant, planning pregnancy, or breastfeeding
  • Significant illness reducing survival probability to 12 months (e.g., metastatic cancer)
  • Known insulin dependent diabetes mellitus
  • Steroid treatment (oral or IV) within past 6 months
  • Receiving workman's compensation
  • Receiving prescription narcotic medication
  • Involved in litigation related to musculoskeletal injuries or disorders
  • Prisoner or pending incarceration
  • Comorbidities affecting participation or results (e.g., autoimmune disorders, HIV, neuropathic pain, fibromyalgia, restless leg syndrome, active infection, chronic pain management)
  • Significant psychiatric disorders (major depression, anxiety disorders, bipolar disorder, schizophrenia)
  • Substance or alcohol dependence or abuse
  • Participating in another drug or device study that may interfere
  • Claustrophobia or implanted metallic devices contraindicating MRI
  • Known allergy or hypersensitivity to investigational device materials

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Fraser Orthopaedic Institute

New Westminster, British Columbia, Canada, V3L OE4

Actively Recruiting

2

University of British Columbia

Vancouver, British Columbia, Canada, V6T 1Z4

Actively Recruiting

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Research Team

C

Chief Clinical Officer

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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