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Motor Evoked Potentials With Modified Facilitation Technique

Not Applicable
Completed
Conditions
Multiple Sclerosis
Interventions
Diagnostic Test: MEP using standard facilitation technique
Diagnostic Test: MEP using modified facilitation technique
Registration Number
NCT03646929
Lead Sponsor
University Hospital, Basel, Switzerland
Brief Summary

Investigating the change in Test- Retest- reliability in healthy individuals when applying a modified easy to use facilitation technique compared to standard facilitation technique and analyzing sensitivity and specificity in patients with multiple sclerosis regarding detection of pathologic results

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
81
Inclusion Criteria

Not provided

Exclusion Criteria
  • Contraindication for measuring of motoric evoked potentials (MEP): metal implants (pacemaker, stents); known epilepsy oder previous epileptic fit
  • Known disease of the peripheral nervous system (polyneuropathy)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
healthy individuals and patients with multiple sclerosisMEP using standard facilitation techniqueMEP in healthy individuals and patients with multiple sclerosis are measured using standard facilitation technique
patients with multiple sclerosisMEP using standard facilitation techniqueMEP in patients with multiple sclerosis are measured using modified facilitation technique
patients with multiple sclerosisMEP using modified facilitation techniqueMEP in patients with multiple sclerosis are measured using modified facilitation technique
Primary Outcome Measures
NameTimeMethod
Change in Test- Re-Test reliability when using modified facilitation technique (compared to standard facilitation technique) in healthy individualsmeasuring time 2 (75 minutes) maximal 1 month later than measuring time 1 (75 minutes)

Determination of mean intra-individual difference between measuring time 1 and measuring time 2 and calculation of standard deviation

comparison of sensitivity and specificity of modified facilitation technique and standard facilitation technique in patients with multiple sclerosis1 measuring time (90 minutes)

Determination on the basis of the standard values (established in healthy individuals) in how many patients a pathological result with the modified facilitation technique and the standard facilitation technique is present. Using a a cross-tabulation, the sensitivity and specificity of the modified facilitating technique compared to the standard facilitation technique is measured

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Dep. of Neurology and Clinical Neurophysiology , Hospital of the University of Basel

🇨🇭

Basel, Switzerland

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