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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
Jochen Vehoff
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

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

First Posted
January 27, 2014
Last Updated
March 30, 2016
Sponsor
Jochen Vehoff
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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

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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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