Could a joint injection of growth hormone and Platelet-Rich plasma offer a new path for arthritis relief?
NCT ID NCT06907121
First seen Aug 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time
Summary
This trial is testing whether injecting a combination of growth hormone and platelet-rich plasma directly into the joint can improve pain, stiffness, and function in adults with knee or ankle arthritis that hasn't responded to usual treatments. Half of the 192 participants will receive the active injections, while the other half will get a saline placebo, with five injections given over a few weeks. The study measures success by looking for at least a 30% improvement in joint-specific scores at six months after the final injection, and also checks for structural changes on MRI. If it works, this approach could become a non-surgical option for people with resistant arthritis.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Intra-articular injections of recombinant human growth hormone (somatropin) combined with platelet-rich plasma (PRP)
- What this could lead to
- If successful, this could offer a non-surgical treatment option for people with knee or ankle arthritis that hasn't responded to standard care, potentially reducing pain and improving mobility.
- What could go wrong
- This is an early-phase trial, so the treatment may not prove more effective than placebo. Injections carry risks like pain, swelling, or infection, and results may not apply to all arthritis patients.
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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Phase 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
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About 192 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Nov 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
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 to 70 years
- 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 include: * Ankle/Knee arthritis resistant to treatment in GP clinic setting. * Radiographically confirmed cartilage injury with Kellgren-Lawrence grade 1-3 can be shown on MRI scan or weight bearing X-Ray within 6 months of study application. * Able to give informed consent to participate in a clinical trial. * Able to commit to attending a clinic for follow up. Exclusion Criteria: Known contraindications for ARTG registered somatropin from various manufacturers (Humatrope, Genotropin) have been used to guide the development of somatropin-related exclusion criteria. Exclusion criteria include: * A known hypersensitivity to any of the components of the product. * Cancer diagnosis or suspicion. * Resected or active tumour. * Skeletally immature (\<18 years of age or no radiographic evidence of closure of epiphyses). * Pregnancy/breastfeeding (participants of childbearing potential need negative pregnancy test in prior screening and agreed upon method of contraception throughout duration of study) * Active infection at the injection site. * Open soft tissue injury. * Metabolic disorders known to adversely affect the skeleton (e.g. renal osteodystrophy or hypercalcemia), other than primary osteoporosis or diabetes. * Over 70 years of age. * Unstable joint or maligned joint \> 5 degrees. * Severe osteoarthritis (Kellgren-Lawrence grade 4 on baseline imaging), including bone-on-bone joints with no detectable cartilage. * Known hypersensitivity to citrate or somatropin. * Unable to give informed consent. * Unable to commit to attend clinic for all follow ups.
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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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Integrant Office
Potts Point, New South Wales, 2011, Australia
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