Optimization of the recording of the CMAP scan and assessment of its reproducibility

Recruiting

• Conditions: -; 10029317

• Registration Number: NL-OMON31026
• Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 13 May 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 12

Inclusion Criteria

age 20-80
normal nerve conduction study of the median nerve
written informed consent

Exclusion Criteria

neurological disease
Any psychological, familial, sociological and geographical condition potentially hampering compliance with the study protocol. Judgment is up to the investigator.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Optimal aquisition parameters for the CMAP Scan, subject discomfort and<br /><br>reproducibility.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>-</p><br>