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A study on peripheral motor nerve excitability in patients with ALS

Completed
Conditions
ALS
Amyotrofische Laterale Sclerose
Registration Number
NL-OMON25730
Lead Sponsor
Centre for Human Drug Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
18
Inclusion Criteria

1.Ability to understand the purpose and risks of the study and provide signed and dated informed consent.

2.Aged 18 to 80 years old, inclusive, at the time of informed consent.

Exclusion Criteria

1.History of diabetes or neuropathy.

2.History of neuromuscular disorders (other than ALS) including but not limited to ALS mimic syndromes, myopathy, myasthenia gravis, and other motor neuron diseases.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate the test-retest reliability of nerve excitability threshold tracking in patients with ALS.
Secondary Outcome Measures
NameTimeMethod
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