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Could one knee injection replace three? new trial tests simpler treatment

NCT ID NCT07352540

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Updated 1 time

Summary

This study compares a single large injection of hyaluronic acid to three smaller weekly injections for knee osteoarthritis. Researchers want to see if the one-shot approach is as safe and effective at reducing pain and improving knee function. The trial involves 46 adults aged 40-70 with moderate to severe knee osteoarthritis.

What this could mean

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

Active substance
hyaluronic acid (HA) injection
What this could lead to
If the single injection works as well as three, it could offer a simpler, more convenient treatment option for knee osteoarthritis.
What could go wrong
This is a small, early-phase study with only 46 participants. The single injection may not provide the same pain relief as the triple regimen, and results may not apply to all 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

Phase 2/3

Runs two stages together: whether the treatment works, then large-scale confirmation.

Participants

About 46 people

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

Started

Jan 2026

Expected to finish

Sep 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

40 to 70 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: * Adults aged 40-70 years * Radiographically confirmed moderate to severe knee osteoarthritis * Knee pain for ≥3 months * Pain on ≥50% of days in past 30 days * Able to provide informed consent Exclusion Criteria: * Grade 4 osteoarthritis (full-thickness cartilage loss) * Non-osteoarthritic knee pain * Other rheumatic diseases (e.g., rheumatoid arthritis, fibromyalgia) * HA injection \<6 months or corticosteroid injection \<3 months in target knee * Recent trauma or surgery of affected knee (\<6 months) * Coagulopathy or bleeding disorder * Autoimmune or relevant systemic disease * Dermatologic infection at injection site * Pregnancy or lactation * Opioid or oral corticosteroid use * Contraindications to MRI (pacemaker, intracorporeal metal, claustrophobia) * Expected absence during study period or noncompliance

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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.

Contacts and locations

Locations

  • Institute of Radiology, University Hospital Erlangen

    Erlangen, 91052, Germany

More trials for these conditions

Other studies related to the condition(s) this trial covers.