Diagnostic Value of a Biomarker of Non-surgical Knee Osteoarthritis

NCT ID: NCT04324554

Last Updated: 2022-12-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

130 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-08-31

Study Completion Date

2024-09-30

Brief Summary

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Osteoarthritis is a very common pathology, especially in an aging population, and a source of disability. Based on standard radiography, the diagnosis is performed late based on the loss of the cartilage thickness. In this context, prosthetic replacement of the joint is a frequent outcome. New diagnostic biomarkers and herapeutic targets are therefore logically research priorities identified by the European League Against Rheumatisms, osteoarthritis ad hoc committee. The inflammation related to the development of this pathology is mainly studied at the cellular level and essentially in animals. Since inflammatory and vascular phenomena are closely intertwined, medical imaging of the subchondral bone vascularization appears interesting.

The dynamic contrast-enhanced T1 Dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) technique allows the identification of changes in the osteoarthritic subchondral bone vascularization. In osteoarthritic animals, these changes could be identified before the cartilaginous lesions became visible, and could be correlated with the severity of osteoarthritis.

This study would be the first to correlate subchondral bone perfusion measurements (performed with the DCE sequence) of early cartilaginous lesions of the knee, identified by non-invasive MRI (T2 mapping) in humans. This examination will be performed on a 3 Tesla MRI.

If a correlation is demonstrated in the early stages of osteoarthritis in both humans and animals, then infusion of subchondral bone could become a biomarker of osteoarthritis, and serve as a follow-up evaluation of future treatments.

Detailed Description

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Osteoarthritis is a very common pathology, especially in an aging population, and a source of disability. Based on standard radiography, the diagnosis is performed late because it is based on the loss of cartilage thickness. In this context, prosthetic replacement of the joint is a frequent outcome. New diagnostic biomarkers and new therapeutic targets are therefore logically research priorities identified up today by the European League Against Rheumatisms, osteoarthritis ad hoc committee .

The strictly mechanical nature of osteoarthritis is currently being questioned. Indeed, the primitive role of inflammation in the development of this pathology is more and more discussed. This inflammation is today studied at the cellular level and essentially in animals. Since inflammatory and vascular phenomena are closely intertwined, medical imaging of the subchondral bone vascularization appears interesting.

The dynamic contrast-enhanced T1 Dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) technique allows the identification of changes in the osteoarthritic subchondral bone vascularization. In osteoarthritic animals, these changes could be identified before the cartilaginous lesions became visible, and could be correlated with the severity of osteoarthritis.

In humans, a preliminary investigator study has recently shown that these changes correlate with the importance of osteoarthritic lesions in patients with advanced osteoarthritis. Up to date, no clinical study has so far been initiated to evaluate the diagnostic value of vascularization markers of subchondral bone in early knee osteoarthritis.

In this context, this prospective monocentric study aims to define the role of DCE medical imaging in the diagnosis of early (non-surgical) patella-femoral osteoarthritis.

This study would be the first to correlate subchondral bone perfusion measurements (performed with the DCE sequence) with early cartilaginous lesions, identified by non-invasive MRI (T2 mapping) in humans. This examination will be performed on a 3 Tesla MRI.

If a correlation is demonstrated in the early stages of osteoarthritis in both humans and animals, then infusion of subchondral bone could become a biomarker of osteoarthritis, and serve as a follow-up evaluation of future treatments.

Conditions

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Knee Osteoarthritis

Study Design

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Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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MRI of the right knee

An MRI of the right knee will be done to define the role of imaging in the diagnosis of early femoro-patellar osteoarthritis.

MRI of the right knee

Intervention Type DIAGNOSTIC_TEST

An MRI of the right knee will be done to define the role of imaging in the diagnosis of early femoro-patellar osteoarthritis.

Interventions

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MRI of the right knee

An MRI of the right knee will be done to define the role of imaging in the diagnosis of early femoro-patellar osteoarthritis.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Patients ≥ 18 years old and \< 60 years old
* Asymptomatic at the patella-femoral joint
* Coming to perform a medical imaging examination for another indication, in the medical imaging department of the GHICL
* Patient being informed and given free, informed and written consent to participate
* Affiliated to the social security

Exclusion Criteria

* Medical history of traumatic ligamentous, meniscal or cartilaginous lesion
* Medical history of knee surgery
* Contraindications to MRI (pacemaker, ferromagnetic vascular clip, infusion pump, neurostimulator, cochlear implant, suspicion of metallic foreign body, claustrophobia, ...)
* MRI with gadoteric acid injection in the 7 days preceding the MRI of the knee
* Hypersensitivity to gadoteric acid, meglumine or any drug containing gadolinium, or any other contrast medium
* Medical history of severe allergy, uncontrolled asthma, treatment with beta-blocker
* Renal insufficiency: glomerular filtration less than 30 mL/min
* Pregnant or nursing woman
* Patient under tutorship or curatorship
Minimum Eligible Age

18 Years

Maximum Eligible Age

59 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Lille Catholic University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jean-François BUDZIK, Pr

Role: PRINCIPAL_INVESTIGATOR

Lille Catholic University

Locations

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Lille Catholic Hospitals

Lomme, Nord, France

Site Status RECRUITING

Countries

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France

Central Contacts

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Amélie Lansiaux, Md, PhD

Role: CONTACT

03 20 22 52 69 ext. +33

Anne-Sophie Blain, CRA

Role: CONTACT

03 20 22 57 32 ext. +33

Facility Contacts

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Amélie Lansiaux, Md, PhD

Role: primary

03 20 22 52 69 ext. +33

Anne-Sophie Blain, CRA

Role: backup

03 20 22 57 32 ext. +33

References

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Conaghan PG, Kloppenburg M, Schett G, Bijlsma JW; EULAR osteoarthritis ad hoc committee. Osteoarthritis research priorities: a report from a EULAR ad hoc expert committee. Ann Rheum Dis. 2014 Aug;73(8):1442-5. doi: 10.1136/annrheumdis-2013-204660. Epub 2014 Mar 13.

Reference Type BACKGROUND
PMID: 24625626 (View on PubMed)

Related Links

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https://ard.bmj.com/content/73/8/1442.full

Osteoarthritis (OA) currently affects over 40 million Europeans, with its associated personal suffering and significant economic burden for health systems set to dramatically escalate in a rapidly ageing Europe.

Other Identifiers

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RC-P0081

Identifier Type: -

Identifier Source: org_study_id

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