Evaluation of the Autonomic Nervous System During First-dosing With 0.5mg of Fingolimod (Gilenya) in Patients With Relapsing-remitting MS (ANSG)
Primary Purpose
Multiple Sclerosis, Autonomic Nervous System Dysfunction
Status
Completed
Phase
Phase 4
Locations
Switzerland
Study Type
Interventional
Intervention
Gilenya
Sponsored by

About this trial
This is an interventional basic science trial for Multiple Sclerosis focused on measuring relapsing remitting, multiple sclerosis, fingolimod, Gilenya, autonomic nervous system
Eligibility Criteria
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
Sites / Locations
- Cantonal Hospital St. Gallen
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Gilenya
Arm Description
Autonomic testing during first dose adminstration of Gilenya.
Outcomes
Primary Outcome Measures
RMSSD Normal Breathing
Root Mean Square of the Successive Differences (RMSSD) is one of a few time-domain tools used to assess heart rate variability, the successive differences being neighboring RR or pulse intervals.
It is calculated as the square root of the mean of the squares of the successive differences between adjacent RR intervals or pulse intervals.
In this study pulse intervals were measured non-invasively during five minutes, while subjects were supine, breathing regularly.
Measurements were done at two timepoints t=0 and t=4,5hours. RMSSD was compared between these two timepoints.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02048072
Brief Title
Evaluation of the Autonomic Nervous System During First-dosing With 0.5mg of Fingolimod (Gilenya) in Patients With Relapsing-remitting MS
Acronym
ANSG
Official Title
Funktionelle Evaluation Des Autonomen Nervensystems im Zusammenhang Mit Der Erstmaligen Einnahme Von 0,5mg Fingolimod (Gilenya) Bei Patienten Mit schubförmig Verlaufender Multipler Sklerose
Study Type
Interventional
2. Study Status
Record Verification Date
March 2016
Overall Recruitment Status
Completed
Study Start Date
July 2013 (undefined)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
June 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Jochen Vehoff
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
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".
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis, Autonomic Nervous System Dysfunction
Keywords
relapsing remitting, multiple sclerosis, fingolimod, Gilenya, autonomic nervous system
7. Study Design
Primary Purpose
Basic Science
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
33 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Gilenya
Arm Type
Experimental
Arm Description
Autonomic testing during first dose adminstration of Gilenya.
Intervention Type
Drug
Intervention Name(s)
Gilenya
Intervention Description
Autonomic testing during first dose administration of Gilenya.
Primary Outcome Measure Information:
Title
RMSSD Normal Breathing
Description
Root Mean Square of the Successive Differences (RMSSD) is one of a few time-domain tools used to assess heart rate variability, the successive differences being neighboring RR or pulse intervals.
It is calculated as the square root of the mean of the squares of the successive differences between adjacent RR intervals or pulse intervals.
In this study pulse intervals were measured non-invasively during five minutes, while subjects were supine, breathing regularly.
Measurements were done at two timepoints t=0 and t=4,5hours. RMSSD was compared between these two timepoints.
Time Frame
t-4,5 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jochen Vehoff, MD
Organizational Affiliation
Cantonal Hospital of St. Gallen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cantonal Hospital St. Gallen
City
St. Gallen
State/Province
SG
ZIP/Postal Code
9000
Country
Switzerland
12. IPD Sharing Statement
Learn more about this trial
Evaluation of the Autonomic Nervous System During First-dosing With 0.5mg of Fingolimod (Gilenya) in Patients With Relapsing-remitting MS
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