Osteoarthritis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are 18 years of age or older
- People who have been confirmed by MRI scan to have moderate to severe knee joint wear (grade III or IV) in one knee only
- People whose knee pain is rated at least 3 out of 10 on a standard pain scale
- People with a body mass index (BMI) under 35
- People who are able to give their own informed consent to participate in the study
- People who are covered by a social security or health insurance scheme
Who may not be able to join:
- People who have taken anti-inflammatory medications (NSAIDs) or corticosteroid medicines in the 7 days before joining the trial (note: low-dose aspirin of 160 mg or less per day taken as a blood thinner is generally allowed)
- People who have had a hyaluronic acid injection into the affected knee in the 2 months before joining
- People who have had a PRP (platelet-rich plasma) injection into the affected knee within the past year
- People who have had a corticosteroid injection into the affected knee within the past 5 months (note: corticosteroids given by other routes — such as skin cream, eye drops, or inhaler — affecting a different area of the body may be permitted)
- People currently on blood-thinning (anticoagulant) medication that cannot be safely paused during the injection treatment period
- People who have been diagnosed with any type of cancer in the last 3 years
- People who are pregnant, in labour, or breastfeeding
- People who are under legal guardianship or a court-ordered protection arrangement
- People whose participation may interfere with the study results for any other reason, as judged by the trial doctor (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Jean-Jacques Raymond, MD, Centre Hospitalier Intercommunal Toulon La Seyne sur Mer
Phone: 0483772062
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Functional impact
Can't join this trial?
Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.