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Mechanisms of conduction block and axon loss in immune-mediated polyneuropathies

Mechanisms of conduction block and axon loss in immune-mediated polyneuropathies - n.v.t.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON30674
Enrollment
240
Registered
2007-04-03
Start date
2008-03-07
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

inflammatory neuropathies nerve diseases

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for patients with MMN: 1) weakness and atrophy of the limbs on neurological examination, 2) motor conduction block (CB) on extensive standardized nerve conduction studies according to criteria previously defined by our group. Inclusion criteria for patients with CIDP: 1) presence of progressive or relapsing motor (muscle weakness) or sensory (numbness, tingling) dysfunction of more than one limb (both proximally and distally), 2) hyporeflexia or areflexia of the limbs, 3) abnormalities on nerve conduction studies indicative of demyelination (conduction block, increased temporal dispersion, absent F-waves or increased F- M latency, or reduction of conduction velocity). Inclusion criteria for patients with LMND: 1) weakness, atrophy, and fasciculations in the limbs, 2) electrophysiological evidence of lower motor neuron involvement (denervation and/ or reinnervation) on needle EMG examination in clinically affected and nonaffected muscles without evidence of conduction block.

Exclusion criteria

Exclusion criteria: Exclusion criteria for patients with MMN: 1) objective sensory signs on neurological examination, 2) clinical signs of upper motor neuron involvement (pseudobulbar symptoms, clonus of masseter reflex, hyperreflexia hypertonia or extensor plantar responses of the limbs). Exclusion criteria for patients with CIDP: 1) duration of signs and symptoms shorter than 2 months, 2) elevated (>10/mm3) white cell count of cerebrospinal fluid with elevated protein levels. Exclusion criteria for patients with LMND: 1) history of diseases that may mimic LMND (acute poliomyelitis, spinal radiculopathy, diabetic amyotrophy, thyrotoxicosis or hyperparathyroidism), 2) clinical signs of upper motor neuron involvement (see above), 3) objective sensory signs on neurological examination.

Design outcomes

Primary

MeasureTime frame
-indications of or evidence for activity-dependent conduction block -indications of or evidence for depolarizing conduction block

Secondary

MeasureTime frame
-

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)