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Influence of IVIG on nerve excitability in multifocal motor neuropathy (MMN)

Influence of IVIG on nerve excitability in multifocal motor neuropathy (MMN) - IVIG and excitability in MMN

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON42955
Enrollment
45
Registered
2016-10-05
Start date
2016-11-17
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Multifocal motor neuropathy (MMN). This term is familiar to all MMN patients.

Interventions

excitability-tests.
intravenous immunoglobilin
ion-channel
Multifocal motor neuropathy

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosis of MMN according to internationally accepted criteria of the European Federation of Neurological Societies and Peripheral Nerve Society (EFNS/PNS criteria). 2. One median nerve (left or right) with any of the following findings in the forearm segment: (a) conduction block, defined as segmental reduction of compound muscle action potential (CMAP) area of at least 30% or signs of demyelination: conduction velocity decrease up to 38 m/s or less and/or DML 5.3 ms or more and/or increased CMAP duration prolongation in the forearm of at least 30%; (b) motor axon loss defined as decreased CMAP amplitude of 3 mV or less; (c) normal conduction studies. 3. Treatment with IVIG. 4. Age range will be considered between 18 and 99 years.

Exclusion criteria

Exclusion criteria: 1. Other causes for neuropathy than MMN, including carpal tunnel syndrome (CTS). 2. Use of medication affecting peripheral nerve ion-channel currents.

Design outcomes

Primary

MeasureTime frame
To assess the change in excitability parameters induced by IVIG infusion. This will be achieved by comparing excitability-parameters between the time of maximal weakness (just before the next IVIG infusion) and the time of maximal clinical improvement. .

Secondary

MeasureTime frame
To analyse the correlation between the degree of excitability changes after IVIG infusion, the presence of anti-GM1-antibodies and the degree of clinical improvement.

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)