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A novel neurophysiological measurement (MUNIX) in neuromuscular disorders; test-retest reliability and longitudinal follow up measurements in ALS patients

A novel neurophysiological measurement (MUNIX) in neuromuscular disorders; test-retest reliability and longitudinal follow up measurements in ALS patients - MUNIX in ALS

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON36377
Enrollment
20
Registered
2011-08-18
Start date
2011-05-01
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Lou Gehrig disease

Interventions

None listed

Sponsors

Universitair Medisch Centrum Sint Radboud
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: ALS patients must fulfill not less than the revised El Escorial category for probable, laboratory supported ALS. Symptom onset, defined as onset of weakness, must be less than 14 months ago.

Exclusion criteria

Exclusion criteria: Patients with pure upper motor neuron signs or *suspected ALS* will not be eligible for the study. Any history of major neurological disorders that might influence MUNIX measurements (e.g. polyneuropathy, peripheral nerve damage, paresis of any cause, muscular atrophy) in ALS patients.

Design outcomes

Primary

MeasureTime frame
MUNIX inter-rater and intra-rater variability and reproducibility. Longitudinal relation of MUNIX with the revised ALS functional rating scale (ALSFRS-R).

Secondary

MeasureTime frame
Correlation CMAP and MUNIX with echointensity on baseline and after 6 and 12 months

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)