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Tiny RNA clues may explain bone disease differences

NCT ID NCT03838991

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
Running, but no longer taking on new participants.
Completed This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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

Summary

Fibrous dysplasia is a rare bone disease that causes pain, fractures, and deformities, but its severity varies widely for unknown reasons. This study looked at 24 adults—some with the disease and some without—to see if small molecules called microRNAs in blood and bone tissue are linked to how severe the disease is. The goal was to gather knowledge, not to test a treatment.

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 successful, this could help explain why fibrous dysplasia affects people differently and point toward new ways to monitor or treat the disease.
What could go wrong
This is a small, observational study that does not test any treatment. It may not find clear links between microRNAs and disease severity, and any findings will need much more research to be useful.

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

24 people

The number who actually took part.

Started

Jan 2019

Finished

Mar 2023

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 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: Control population : * men and women, * 18 years-old and over, * consulting a rheumatologist or an orthopedist for arthrosis * have scheduled surgery for hip or knee replacement surgery or any intervention involving the lower limb or upper limb. Patients with Fibrous dysplasia: * men and women, * 18 years-old and over, * with a diagnosis of fibrous dysplasia previously established by a rheumatologist. Exclusion Criteria: * Refusal to participate in the study * Long- term corticosteroids treatment (\> 3 months) * Treated osteoporosis * Chronic inflammatory rheumatism (rheumatoid arthritis, psoriasic arthritis, spondyloarthropathy) * Collagen disease (osteogenesis imperfecta…) * Paget's disease, benign bone tumors * Uncontrolled hypo/hyper-thyroidism, hypo/hyper-parathryoidism * Severe renal impairment (GFR \< 30 ml/min/1.73m2) * Cancer or bone metastases (current or in the past two years) * Paget disease, benign bone tumor (osteoid osteoma, enchondroma …) * Malabsorptive disease (Celiac disease, Whipple's disease, intestinal bypass, short bowel syndrome) and inflammatory bowel disease * Pregnant women or lactating * Psychiatric disorders * Difficulty in understanding French * Not a beneficiary of french social security * Patients protected by law

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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

  • Service de Rhumatologie & INSERM U1033, Pavillon F, Hopital Edouard Herriot

    Lyon, 69437, France

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