Can acupuncture threads ease arthritic knees?
NCT ID NCT07833462
First seen Sep 22, 2026 · Last updated Sep 23, 2026 · Updated 1 time
Summary
Researchers test thread-embedding acupuncture, a technique that places dissolvable thread at acupuncture points, in adults aged 51 to 70 with knee osteoarthritis. Participants receive either the real procedure or a sham version once, and researchers track knee pain, function, and range of motion over eight weeks. The goal is to see whether this targeted approach improves knee health compared with a placebo-like control.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- thread-embedding acupuncture, a technique that places dissolvable surgical thread at acupuncture points
- What this could lead to
- If it works, thread-embedding acupuncture could offer a single-session option to ease knee osteoarthritis pain and improve movement, possibly reducing the need for frequent repeat treatments.
- What could go wrong
- This is a small, single-center study of 44 people, so any benefit may be modest or not hold up in larger trials. Acupuncture carries small risks of soreness, bruising, or infection at the needle sites.
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 44 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 2026
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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51 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: * Male and female patients aged 51 to 70 years. * Clinically and radiologically diagnosed with bilateral knee osteoarthritis according to ACR (American College of Rheumatology) criteria. * Kellgren-Lawrence grade II or III knee osteoarthritis. * NRS (Numeric Rating Scale) score \>3 during activity (activities of daily living or light exercise). * Body Mass Index (BMI) ≥18.5 kg/m². * Knee functional limitations assessable via the KOOS. * Ability to understand and complete the KOOS questionnaire. MMSE score \>23 (normal or no significant cognitive impairment). * Willingness to complete the study and sign the informed consent form. Exclusion Criteria: * History of knee surgery such as total knee replacement, arthroscopy, or ligament reconstruction. * Inflammatory joint disease or autoimmune conditions (e.g., rheumatoid arthritis, gouty arthritis, spondyloarthritis, or lupus arthritis) assessed via clinical symptoms and/or radiological findings. * Presence of a tumor, wound, or local infection at the injection site. * History of peripheral vascular disease, DVT/thromboembolism, aneurysm or pseudoaneurysm, or coagulation/bleeding disorders. * Presence of a blood disorder or use of blood thinners (combination antiplatelet or anticoagulant therapy) with an INR ≤ 2.0; history of spontaneous bleeding, thrombocytopenia, or coagulation disorders. * Uncontrolled diabetes mellitus or severe systemic disease with a random blood glucose (RBG) level ≥200 mg/dL (measured via capillary blood using a glucometer). Random blood glucose (RBG) level ≥200 mg/dL in non-diabetic patients (measured via capillary blood using a glucometer for all study participants). * History of keloids. * Routine use of steroids or NSAIDs, or use of topical analgesics prior to therapy and during the study period. * Not currently receiving intra-articular knee injections (corticosteroids or hyaluronic acid) and has not received them in the last 3 months. * Presence of a Baker's cyst in the popliteal fossa, identified during physical examination. * Patients currently undergoing physiotherapy or who have undergone it within the last month. * Prior receipt of thread-embedding acupuncture therapy in the knee area or at acupuncture points BL40-BL57 within the last 6 months, or other forms of acupuncture within the last 2 weeks. * History of hypersensitivity or allergic reactions to polydioxanone (PDO) threads or procedure needle materials (e.g., stainless steel).
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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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Universitas Indonesia
Jakarta Pusat, DKI Jakarta, 10430, Indonesia
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