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New handheld device could reveal stem cell fate in arthritis treatment

NCT ID NCT07313020

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This early-stage study tests a handheld imaging device that uses magnetic particles to track stem cells after they are injected into the knee. Ten adults with mild-to-moderate knee osteoarthritis will receive a single injection of labeled stem cells, and the device will monitor their location and survival over 30 days. The goal is to see if this new imaging method can better predict treatment success than standard MRI scans.

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

Early phase 1

The earliest testing in people: a first look at safety, in a very small group.

Participants

About 10 people

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

Started

Dec 2025

Expected to finish

Dec 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

18 to 75 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: 1. Diagnosis of knee osteoarthritis according to internationally accepted criteria (e.g., American College of Rheumatology criteria). 2. Age between 18 and 75 years, inclusive. 3. Radiographic Kellgren-Lawrence grade II or III in the target knee. 4. Chronic knee pain of arthritic origin. 5. Absence of local or systemic infection. 6. No contraindications to joint cavity puncture as determined by hematological and biochemical tests. 7. Willing and able to understand the study, provide informed consent, and comply with all study procedures. Exclusion Criteria: 1. Lack of legal capacity or impaired capacity to provide informed consent. 2. Known active infection with HIV, hepatitis B virus, hepatitis C virus, or syphilis (positive serology). 3. Body mass index (BMI) \> 30 kg/m². 4. Congenital or acquired deformity of the target knee. 5. Pregnant or breastfeeding women. 6. History of or current active malignancy. 7. Known immunodeficiency disorder. 8. Intra-articular injection (e.g., corticosteroids, hyaluronic acid) in the target knee within the past 3 months. 9. Concurrent participation in another interventional clinical trial. 10. Any other condition that, in the opinion of the investigator, would make the participant unsuitable for the study (e.g., significant comorbid illness).

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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

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    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

  • Hainan General Hospital

    Haikou, Hainan, China

More trials for these conditions

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