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Validating the Clinical Effect of a Knee Orthosis

Medial Gonarthrosis

The aging population is steadily increasing, partly due to increasing life expectancy. At the same time, chronic diseases, including those affecting the musculoskeletal system (e.g., osteoarthritis), whose prevalence increases with age, limit the daily activities of those affected and thus affect more and more people. Arthrosis is the most common form of these diseases worldwide. According to the l'Institut de la statistique du Québec, nearly one in two Quebecers aged 15 and over is affected by a chronic health problem.

Knee orthosis is one form of treatment that helps patients suffering from knee gonarthrosis. This treatment aims to compensate for certain biomechanical deficits in patients. A variety of joint configurations exists to target specific biomechanical deficits. A constant challenge for companies manufacturing orthoses is transmitting the orthosis's biomechanical effect to the patient. The desired effect requires a change in the forces applied inside the knee, but the orthosis cannot directly transmit forces to the patient's bones due to its external nature to the body. Customization of orthoses is crucial to improve the transmission of the biomechanical effect as well as tolerance to it. O3D Inc. aims to validate the effectiveness of its new custom orthosis for treating knee gonarthrosis symptoms.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 to 75

Participation Criteria

Inclusion Criteria:

* Suffering from medial gonarthrosis
* Receiving a regular model of the O3D orthosis

Exclusion Criteria:

* Suffering from tricompartmental gonarthosis
* Having completed the delivery appointment for a O3D orthosis

Study Location

Topmed
Topmed
Québec, Quebec
Canada

Contact Study Team

Backup Contact

Edith Martin, Phd. metallurgical engineering

Primary Contact

Mathieu Germain Robitaille, M. Sc. in kinesiology

[email protected]
418-683-2104
Backup Contact

Marianne Lancelot, M.Sc

[email protected]
418-683-2104
Study Sponsored By
TOPMED
Participants Required
More Information
Study ID: NCT06655558