Evaluation of the Autonomic Nervous System During First-dosing With 0.5mg of Fingolimod (Gilenya) in Patients With Relapsing-remitting MS
NCT ID: NCT02048072
Last Updated: 2016-04-29
Study Results
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View full resultsBasic Information
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COMPLETED
PHASE4
33 participants
INTERVENTIONAL
2013-07-31
2015-06-30
Brief Summary
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The impact of Gilenya (Fingolimod) on the autonomic nervous system is quantitavely measured, using a state-of-the-art technique. Non-invasive blood pressure measurement is performed with the Finometer Pro (Finapres Medical Systems, NL) under different paradigms (breathing at rest, deep breath, valsalva maneuver, active standing). In addition the sympathetic skin reaction is performed. The non-invasive blood pressure measurements are done by continuous, plethysmographic blood pressure measurement at the index finger, while the patient is performing the tasks mentioned above. By interpreting the blood pressure curve, heart rate and blood pressure variability are calculated. The sympathetic skin reaction consists of measuring the change of electric conductibility of the skin (palms and soles) after an electric stimulus of a peripheral nerve. These parameters allow to assess the functionality of four important autonomic functional systems (orthostasis, sympathetic adrenergic, sympathetic cholinergic, parasympathetic cholinergic). Normative data has been acquired in our lab.
Our hypothethis is, that there will be a change of heart rate variability at t4,5h compared to baseline (t0) for the parameter "RMSSD" under "normal breathing".
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
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Gilenya
Autonomic testing during first dose adminstration of Gilenya.
Gilenya
Autonomic testing during first dose administration of Gilenya.
Interventions
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Gilenya
Autonomic testing during first dose administration of Gilenya.
Eligibility Criteria
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Inclusion Criteria
* treatment with Gilenya intended
* no contraindications for the treatment with Gilanya
* all safety-aspects have been fullfilled
* age between 18 and 60 years
* written consent is given
Exclusion Criteria
* steroids within 30 days before randomization
* heart rhythm disturbance
* new or currently changed dose (last 4 weeks) of bata-blockers, calcium antagonists, antidepressants or antiarrhythmics
* diabetes mellitus
* polyneuropathy
* missing consent
* pregnancy
* lactation period
18 Years
60 Years
ALL
No
Sponsors
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Jochen Vehoff
OTHER
Responsible Party
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Jochen Vehoff
Dr. med. Jochen Vehoff
Principal Investigators
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Jochen Vehoff, MD
Role: PRINCIPAL_INVESTIGATOR
Cantonal Hospital of St. Gallen
Locations
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Cantonal Hospital St. Gallen
Sankt Gallen, Canton of St. Gallen, Switzerland
Countries
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Other Identifiers
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ANSG 1.8
Identifier Type: -
Identifier Source: org_study_id
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