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Prolonged repetitive nerve stimulation (RNS) in myasthenia gravis (MG) and Lambert-Eaton myasthenic syndrome (LEMS): quantitative and relevant.

Prolonged repetitive nerve stimulation (RNS) in myasthenia gravis (MG) and Lambert-Eaton myasthenic syndrome (LEMS): quantitative and relevant. - Prolonged RNS in myasthenia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON31264
Enrollment
40
Registered
2007-10-11
Start date
2007-09-15
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

myasthenia MG LEMS

Interventions

None listed

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: over 18 years old MG: clinical signs and symptoms of MG, positive for anti-AChR antibodies and characteristic RNS EMG abnormalities (decrement over 10%) or abnormal Single Fibre EMG. LEMS: clinical signs and symptoms of LEMS, positive for anti-VGCC antibodies and characteristic RNS EMG abnormalities (decrement over 10% and increment over 60%) or abnormal Single Fibre EMG.

Exclusion criteria

Exclusion criteria: anticoagulant drugs muscle and nerve diseases or diseases predisposing to nerve or muscled isease, for example diabetes mellitus

Design outcomes

Primary

MeasureTime frame
CMAP-amplitude and change of amplitude after prolonged stimulating and recording. Is hte pattern different between controls itselves and between controls and patients?

Secondary

MeasureTime frame
Is the technique painless indeed?

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)