Knee pain relief without surgery? PRP injections tested against standard care
NCT ID NCT07016672
First seen Jun 24, 2026 · Last updated Jul 08, 2026 · Updated 3 times
Summary
This study tests whether injections of platelet-rich plasma (PRP) work better than hyaluronic acid (HA) for people with advanced knee osteoarthritis (grades III or IV). 150 participants will receive three injections of either PRP or HA and be followed for a year. The goal is to see which treatment reduces pain and improves knee function more.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Platelet-rich plasma (PRP) and hyaluronic acid (HA)
- What this could lead to
- If PRP works better than HA, it could offer a longer-lasting, non-surgical option for people with advanced knee osteoarthritis who cannot have surgery.
- What could go wrong
- This is a small, early-stage study with no blinding, so results may be biased. PRP is not yet proven for advanced osteoarthritis, and benefits may be modest or temporary.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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Oct 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age ≥ 18 years ; 2. MRI confirmed grade III or IV unilateral gonarthrosis ; 3. Pain ≥ 3/10 on the visual analogue scale (VAS); 4. Patient with a BMI \< 35 5. Patient capable of giving consent prior to participation in the study; 6. Affiliated or entitled under a social security scheme. Exclusion Criteria: 1. Non-steroidal anti-inflammatory drugs\* or corticosteroids\*\* taken in the 7 days prior to inclusion; 2. Local injection of hyaluronic acid in the 2 months prior to inclusion; 3. Local injection of PRP within 1 year prior to inclusion; 4. Local injection of corticosteroids within 5 months prior to inclusion; 5. Current anticoagulant treatment that cannot be stopped during the hyaluronic acid or PRP injection protocol period; 6. Patient diagnosed with any type of cancer in the last 3 years; 7. Pregnant women, women in labour or breast-feeding women; 8. Patients under judicial protection (guardianship, curatorship, etc.) or safeguard of justice; 9. Any other reason which, in the opinion of the investigator, could interfere with the evaluation of the study objectives. * Acetylsalicylic acid is allowed when it is prescribed as an antiplatelet agent at doses lower than or equal to 160 mg per day. It has, indeed, no anti-inflammatory effect at these doses. * Corticosteroids can be administered when they have a local action different from the one applied to the treated knee (cutaneous, instiled or inhaled routes).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Centre Hospitalier Intercommunal de Toulon- La Seyne sur Mer - Hôpital Sainte Musse
RECRUITINGToulon, Var, 83100, France
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