About this trial

This prospective cohort study is part of the Clinnova programme and aims to (i) identify clinical imaging and omics characteristics associated with early Multiple Sclerosis (MS) and with transitioning phases to progressive MS, as well as (ii) to investigate digital biomarkers allowing the continuous clinical monitoring of those patients.

Eligibility criteria

Qualifiers

Age ≥18

Participants are willing and able to comply with the protocol, including undergoing data and samples collection as well as study visits and examinations.

Signed informed consent form

In possession of a Healios+Me app compatible smartphone (iOS/Android)

Disqualifiers

None

Trial design

Treatments tested in this trial

  • All participants will be asked to provide data and samples for collection and analysis.

Treatment groups

100 Participants
are divided into 1 treatment group

Locations

1
Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB)4031, Basel Switzerland

Sponsors and collaborators

University Hospital, Basel, Switzerland

Lead sponsor

Luxembourg Institute of Health

Collaborator

Research Center for Clinical Neuroimmunology and Neuroscience Basel

Collaborator