A study on peripheral motor nerve excitability in patients with ALS
Completed
- Conditions
- ALSAmyotrofische 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
Name Time Method To evaluate the test-retest reliability of nerve excitability threshold tracking in patients with ALS.
- Secondary Outcome Measures
Name Time Method