If you decide to participate, the first step is signing an Informed Consent Form. This document explains the study details, procedures, potential risks, and your rights as a participant. Our research team will guide you through every step and answer any questions you may have.
Once consent is provided, you’ll undergo a screening visit that includes medical evaluations and an MRI of your knee. This MRI will determine eligibility based on specific bone-shape measurements used in osteoarthritis research.
If eligible, you will be randomly assigned to either the investigational treatment group or the placebo group. All injections are administered by trained professionals using imaging guidance to ensure accuracy and safety.
You will attend several follow-up appointments for approximately one year. These visits allow our team to monitor your symptoms, evaluate your knee structure with MRI, and track changes in mobility and comfort levels.
* Study-related care is offered at no charge. Expert physicians and healthcare professionals conduct thorough physical exams and assessments.
