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

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

33 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-07-31

Study Completion Date

2015-06-30

Brief Summary

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This study is designed to primarily evaluate the impact of Gilenya (Fingolimod) on the autonomic nervous system in patients being treated for the first time with Gilenya (Fingolimod). Effects on the cardiovascular system will be studied as well. The study is conducted to answer the question, if, and if yes, what impact the treatment with Gilenya (Fingolimod) has on the autonomic nervous system. To our knowledge little is known about the effects of Gilenya (Fingolimod) on the autonomic nervous system. We do know of rare, but potentially clinically and therapeutically relevant cardiovascular adverse events of Gilenya (Fingolimod). From a scientific point of view the mechanisms by which this is mediated are of interest. Maybe a better understanding of these mechanisms might even be of clinical relevance (e.g. risk stratification).

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".

Detailed Description

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Conditions

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Multiple Sclerosis Autonomic Nervous System Dysfunction

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Gilenya

Autonomic testing during first dose adminstration of Gilenya.

Group Type EXPERIMENTAL

Gilenya

Intervention Type DRUG

Autonomic testing during first dose administration of Gilenya.

Interventions

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Gilenya

Autonomic testing during first dose administration of Gilenya.

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* indication for treatment with Gilenya according label
* 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

* relapse during the last 30 days befor randomization
* 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
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Jochen Vehoff

OTHER

Sponsor Role lead

Responsible Party

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Jochen Vehoff

Dr. med. Jochen Vehoff

Responsibility Role SPONSOR_INVESTIGATOR

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

Site Status

Countries

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Switzerland

Other Identifiers

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ANSG 1.8

Identifier Type: -

Identifier Source: org_study_id

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