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Treatment of Lambert-Eaton myasthenic syndrome with 3,4-diaminopyridi

Not Applicable
Recruiting
Conditions
ambert-Eaton myasthenic syndrome
Registration Number
JPRN-UMIN000024055
Lead Sponsor
Tokushima University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
10
Inclusion Criteria

Not provided

Exclusion Criteria

Minors, pregnant women, or patients with a past history of epilepsy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The compound muscle action potential(CMAP) and the degree of increase in CMAP amplitude after high frequency receptive nerve stimulation conducted 1, 2, 4 months after treatment.
Secondary Outcome Measures
NameTimeMethod
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