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Evaluating the effect of trans cranial direct current stimulation on myasthenia gravis

Phase 2
Conditions
Myasthenia gravis.
Myasthenia gravis
G70.0
Registration Number
IRCT20181109041598N1
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
15
Inclusion Criteria

patients who were diagnosed through medical criteria and laboratory tests were referred by a neurologist
patients who were under MG treatment for at least 3 months prior to the study.
under the medication with or without thymectomy
The average age is 18 to 40 years old

Exclusion Criteria

Being pregnant
psychological or neurological disorders
MG crisis for at least 3 month prior to the study
Having unsightly sleep on the night before the test and having a high fatigue on the day of the test
Any history of consuming nicotine and substance abuse
using caffeine in less than 5 hours

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Muscular function of myasthenia gravis. Timepoint: In two rounds of the first and second sessions. Method of measurement: Quantitative Myasthenia Gravis (QMG)for Quantitative Measurement of Disease Symptoms, mannual mucle testing (MMT) for measuring muscle strength and MG-QOL15 (myasthenia gravis quality of life) for assessing the quality of life of a person with MG.
Secondary Outcome Measures
NameTimeMethod
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