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Blood and knee fluid hold clues to why arthritis worsens

NCT ID NCT07833488

What the study statuses mean

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Recruitment status, easiest to join first

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 Results may not be published yet.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

Expanded access (not trials)

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Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
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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

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Status unknown
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First seen Sep 22, 2026 · Last updated Sep 23, 2026 · Updated 1 time

Summary

Researchers at Imperial College London are following 200 adults with early knee osteoarthritis, a degenerative meniscal tear, or a prior acute knee injury. The study collects blood, saliva, or knee fluid samples and asks participants about knee pain, function, and activity through yearly questionnaires for up to five years. X-rays at baseline and again around year two or three track joint changes. The goal is to find markers or genetic factors that might explain why knee osteoarthritis improves or worsens.

What this could mean

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

What this could lead to
If researchers find markers in blood or knee fluid that track worsening osteoarthritis, doctors could one day spot the disease earlier and test treatments before joint damage sets in.
What could go wrong
This is an observational study, so it cannot prove that any marker causes osteoarthritis or that acting on it helps. Findings from 200 people may not apply to everyone, and five years of follow-up may not capture the full course of the disease.

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.

Participants

About 200 people

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

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Jul 2031

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.

Who is studied

Participants will be recruited across Imperial College Healthcare NHS Trust (ICHNT) through four primary pathways: 1. Elective Orthopaedic Lists: Patients scheduled for relevant procedures on elective orthopaedic surgical lists. 2. Outpatient Procedural Lists: Patients scheduled for joint drainage or intra-articular injections within musculoskeletal specialties, including rheumatology, sports and exercise medicine, and musculoskeletal radiology. 3. Participants from existing research cohorts, such as the Imperial College Healthcare Tissue Bank (ICHTB), i.e., i-Bank, who are eligible and have previously consented to be re-contacted for future studies. 4. Research Registries: Individuals identified via research registries and mailing lists, including the Imperial Joint Health: Understanding, Monitoring and Prevention (JUMP) Registry, the Northwest London Health Research Register, and the Imperial Health Knowledge Bank (IHKB).

Ages

18 years and older

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: ALL participants must meet the following criteria: * Male or female, aged ≥18 years of age AND at least one of the following (a-d): 1. A definite diagnosis of knee osteoarthritis , evidenced by consistent knee symptoms and imaging findings, commensurate with non-advanced KL grade changes (KL 0-2 where an X-ray grade is available) 2. A symptomatic degenerative meniscal tear with or without definite imaging findings suggesting knee osteoarthritis 3. Probable early-stage symptomatic knee osteoarthritis without definite imaging changes, fulfilling NICE diagnostic criteria for osteoarthritis: * Age 45 or over * Activity-related knee pain. * Either no morning stiffness or that lasts \<30 minutes 4. A definite clinically significant acute knee injury at the age of 50 or younger at any stage in the past, evidenced by appropriate clinical history of a traumatic knee episode AND documented imaging or surgical confirmation of a relevant structural injury. * Willing to provide at least one of the following samples: synovial fluid or blood (a salivary sample is an acceptable alternative for remote participants with a history of knee injury. This alternative also applies to existing participants from ICHTB/IHKB, for whom no prior DNA sample is currently banked) * Understand English sufficiently to be able to read PIS, ICF and/or Participant Invitation Letter * Provide an ICF, signed by the participant * Be capable of complying with Protocol requirements, i.e. completing study questionnaire packs. Exclusion Criteria: * Known advanced radiographic changes of KOA on available imaging (KL grade 3-4 where available), or other commensurate findings, such as those present on MRI * Knee joint replacement (uni-compartmental arthroplasty or total knee arthroplasty) of the index knee, prior to consent, or planned during current episode of care, or within next 12 months * Other clinically significant knee pathology such as infection or malignancy affecting the index knee joint or surrounding bone (at any time) * Surgery to the index knee in the last 3 months * Any other systemic inflammatory disease (e.g. inflammatory bowel disease), systemic infection, or inflammatory arthritis (e.g. rheumatoid arthritis, psoriatic arthritis, gout) * Systemic/intra-articular steroid use to index knee in the last 3 months * Any use of immunosuppressive drugs or chemotherapy in the last 12 months * Unwilling or unable to provide follow-up data for minimum 2 years and/or maximum 5 years * Pregnancy, expecting to be pregnant, near the scheduled Year 2 or Year 3 X-ray visit. * Other medical reason which would prevent participation, at the discretion of the investigator.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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How to take part

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  1. The study's own enquiry address

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  2. The places running it

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

  3. The official record

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    Open the record ↗

  4. A doctor treating you

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Contacts and locations

Study contacts

  • Contact

    Email: •••••@•••••

Locations

  • Centre for Inflammatory Disease, 9th Floor, Commonwealth Building, Imperial College London, Department of Immunology and Inflammation, Hammersmith Campus, Du Cane Road, London

    London, W12 0NN, United Kingdom

    Contact Email: •••••@•••••

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