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MRI for MMN and CIDP - Towards improved diagnostic accuracy and dissection of pathophysiology.

MRI for MMN and CIDP - Towards improved diagnostic accuracy and dissection of pathophysiology. - MIMIC

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON48985
Enrollment
190
Registered
2018-07-11
Start date
2018-09-05
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

immuun-mediated/treatable polyneuropathy

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Age 18- 80 years. 2. Patients: confirmed diagnosis of CIDP or MMN, as defined by relevant diagnostic consensus criteria. 3. Disease controls: established diagnosis of relevant clinical mimic to diagnosis CIDP and MMN (CMT, lower motor neuron syndromes and axonal neuropathies). 4. Healthy volunteers: no previous diagnosis, sign/symptoms consistent with neuropathy

Exclusion criteria

Exclusion criteria: 1. age 80 years, 2. physically unable to undergo MRI or HRUS of the peripheral nervous system

Design outcomes

Primary

MeasureTime frame
The main study parameters for objective 1, are: 1. (Semi-)quantitative rating of MRI-imaging of brachial plexus. 2. Cross-sectional area (CSA) on HRUS imaging (CSA measurements of median nerves and brachial plexus). These parameters will be used to select those with highest diagnostic yield as endpoint. The main parameters for objective 2, are: 1. MRI-DTI values (radial, axial and mean diffusivity (RD, AD and MD), fractional anisotropy (FA)). The will be used to determine the distribution of parameters and nerve size that may be useful in the future for patients with CIDP and MMN.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)