About this trial
This study aims to characterize the clinical features, frequency of different subgroups of MG, and identify predictors of treatment responsiveness among different subgroups of MG. The predictors are including primary outcome (percentage of changes in MG scales at baseline at time of enrollment and after 3 months) and secondary outcome (treatment-related adverse events). Also it aims to determine the frequency of patients with refractory MG.
This information will be used to understand the trends and mechanisms of disease relapse, and optimal management strategies.
Eligibility criteria
Qualifiers
Age from 16 years and older.
Gender: both sexes are included.
unequivocal clinical response to pyridostigmine
decrement >10% in repetitive nerve stimulations study (RNS).
Disqualifiers
Age younger than 16 years.
History of chronic psychiatric or neurological disorder other than MG that can produce weakness or fatigue.
Severe systemic illness affecting life-expectancy.
Trial design
Treatments tested in this trial
- Drug treatment of myasthenia gravis and treatment of crisis