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Portable ultralow field MRI in early arthritis

Towards stratified management of early arthritis patients using a portable, ultralow field MRI - Portable ultralow field MRI in early arthritis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON58318
Enrollment
655
Registered
2025-10-07
Start date
2026-04-08
Completion date
Unknown
Last updated
2026-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

rheumatoid arthritis, early arthritis, inflammatory arthritis arthritis

Interventions

Patients with early arthritis aged =18 and who consent with the BioBank “Reumatische Klachten in the LUMC (locally also known as Early Arthritis Clinic (EAC)
running since 1993) will be asked to undergo this non-invasive portable MRI at baseline. Inclusion of patients will continue until a total sample size at baseline of 546 patients is reached. Follow-up

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria for this study are similar to the inclusion criteria for the EAC/Biobank “Reumatische Klachten”, namely Patients aged =18 years with presence of synovitis determined at physical examination by a rheumatologist and a symptom duration <2 years.

Exclusion criteria

Exclusion criteria:  An obvious diagnosis of gout or osteoarthritisDespite of the low field strength, people with pacemakers or specific metal implants cannot participate. Also women who might be pregnant cannot participate.

Design outcomes

Primary

MeasureTime frame
 The main endpoint is the absence of persistent inflammatory arthritis, defined as either the absence of persistent clinical arthritis without having started DMARD therapy, or in case DMARD therapy was initiated, the development of sustained DMARD-free remission, defined as the persistent absence of clinical arthritis after DMARD cessation with a minimal follow-up duration of 1 year after DMARD stop. 

Secondary

MeasureTime frame
Additionally to the outcome described above, we will also assess the amount of patients fulfilling the 2010 RA classification criteria after 1 year of follow-up.

Countries

Netherlands

Contacts

Public ContactA.H.M. van der Helm-van Mil

Leids Universitair Medisch Centrum

EAC@lumc.nl071 5263423

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: May 22, 2026