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New Blood-Based injection could beat PRP for knee pain

NCT ID NCT06932614

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 26, 2026 · Updated 1 time

Summary

This study tests whether a new, concentrated version of a patient's own blood platelets (called self-repair factor) works better than standard platelet-rich plasma (PRP) injections for knee osteoarthritis. 90 adults with mild to moderate knee arthritis will receive either the new factor, PRP, or a placebo. The goal is to see which treatment best reduces pain and improves knee function over six months.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Lyophilized self growth factor (a concentrated form of the patient's own blood platelets)
What this could lead to
If it works, this could offer a more effective injection treatment for knee osteoarthritis pain and stiffness, potentially better than current PRP therapy.
What could go wrong
This is a small, early-stage trial with only 90 people. The new treatment may not prove better than PRP or placebo, and individual results vary.

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

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

About 90 people

The number the study aims to enrol. It can still change while the study runs.

Started

Aug 2025

Expected to finish

Jul 2026

An estimate. End dates often move.

Lead sponsor

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

20 to 80 years

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Male or female, aged over 20 and under 80. * Consciousness clear and able to communicate. * Unilateral or bilateral osteoarthritis of the knee with symptoms lasting more than 3 months. * X-ray imaging shows mild to moderate knee osteoarthritis (Kellgren-Lawrence grades 1-3). * Knee joint pain with a Visual Analogue Scale (VAS) score greater than 4. Exclusion Criteria: * Severe knee osteoarthritis (Kellgren-Lawrence grade 4). * Currently systemic infection. * Received hyaluronic acid or corticosteroid intraarticular injections within the past six months, or received NSAIDs or oral corticosteroid treatment within 7 days prior to treatment. * The treated joint has undergone joint replacement surgery or major surgery. * Severe knee deformity or instability. * Known history of cancers, rheumatoid arthritis, platelet dysfunction, thrombocytopenia, hypofibrinogenemia, acute or chronic infectious diseases, chronic liver disease, or poorly controlled cardiovascular disease or diabetes. * Currently receiving anticoagulant therapy. * Long-term or excessive use of aspirin or vitamin E. * History of HIV/AIDS, syphilis, or other legally notifiable infectious diseases. * Pregnant or breastfeeding women, or women and men of childbearing potential who are unable to use effective contraception during the treatment period. * Deemed unsuitable for participation in the trial by the principal investigator. * Unable to sign the informed consent form.

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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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • No. 325, Sec. 2, Chenggong Rd., Neihu Dist.

    RECRUITING

    Taipei, 114, Taiwan

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