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Clinical Trials/NCT03851770
NCT03851770
Unknown
Not Applicable

NEURO-LARYNX:Laryngeal Motor Evoked-potentials as a Biomarker of Vagus Nerve Stimulation

Cliniques universitaires Saint-Luc- Université Catholique de Louvain1 site in 1 country10 target enrollmentDecember 27, 2018
ConditionsEpilepsy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Epilepsy
Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Enrollment
10
Locations
1
Primary Endpoint
Laryngeal motor evoked potential (LMEP)
Last Updated
7 years ago

Overview

Brief Summary

The goal of this study is to record and characterize larynx evoked motor potentials induced by vagus nerve stimulation. This study will include 10 adult patients implanted with a Vagus nerve stimulator, followed at the Center for Refractory Epilepsy at Cliniques St Luc. The inclusion criteria are: (1) patient aged between 18 and 65 years ; (2) cervical VNS device (Cyberonics, Houston, TX, USA) implanted for at least 6 months, (3) normal electrode impedance of the electrode. Exclusion criteria are (1) presence of a concomitant laryngeal pathology or recurrent laryngeal nerve damage, independent from VNS ; (2) important VNS side effects reported by the patient, such as severe dyspnea (grade III-IV) or severe pain in the neck/ear region.

Registry
clinicaltrials.gov
Start Date
December 27, 2018
End Date
September 30, 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • patients aged between 18 and 65 years
  • Vagus nerve stimulation implanted for at least 6 months
  • No impedance issues with the VNS electrode

Exclusion Criteria

  • presence of a concomitant laryngeal pathology or RLN damage, independent from vagus nerve stimulation
  • important side effects of the VNS reported by the patient such as dyspnea, pain in neck/ear region and gastrointestinal complaints.

Outcomes

Primary Outcomes

Laryngeal motor evoked potential (LMEP)

Time Frame: the LMEP is recorded for 60 minutes from the moment the patient arrives to the clinic to perform the test

Characteristics of the laryngeal motor evoked potential Threshold : the mA of current output necessary for evoking the LMEP Latency : the time between the negative peak of the stimulation artifact and the first positive deflection of the LMEP Amplitude : the difference in μV between the lowest negative and the highest positive peak of the LMEP Duration : the time between the first positive deflection of LMEP and the return to the noise level Dose- response curve: the relation between increasing intensity of vagal nerve stimulation and amplitude of the LMEP

Study Sites (1)

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