Clinical Impact Through AI-assisted MS Care - A Retrospective Multi-center Observational Study.

NCT06280755 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 7000

Last updated 2025-12-12

No results posted yet for this study

Summary

The RECLAIM study aims to gather a centralized and harmonized dataset, enabling the secondary use of data for building AI-based models that will support diagnosis and prognosis of individual Multiple Sclerosis patient's disease course and treatment response in a real-world setting. Additionally, the data will be used to generate further insights on Multiple Sclerosis progression as well as to develop the tools to monitor this progression.

Conditions

  • Multiple Sclerosis
  • NMO Spectrum Disorder
  • Myelin Oligodendrocyte Glycoprotein Antibody-associated Disease
  • Radiologically Isolated Syndrome
  • Clinically Isolated Syndrome

Sponsors & Collaborators

  • Charite University, Berlin, Germany

    collaborator OTHER
  • Ruhr University of Bochum

    collaborator OTHER
  • Technische Universität Dresden

    collaborator OTHER
  • University Hospital, Lille

    collaborator OTHER
  • Casa di Cura IGEA

    collaborator OTHER
  • General University Hospital, Prague

    collaborator OTHER
  • Hoffmann-La Roche

    collaborator INDUSTRY
  • Bristol-Myers Squibb

    collaborator INDUSTRY
  • Imcyse SA

    collaborator INDUSTRY
  • AB Science

    collaborator INDUSTRY
  • Nocturne UG

    collaborator UNKNOWN
  • Aalto University

    collaborator OTHER
  • icometrix

    lead INDUSTRY

Principal Investigators

  • Friedemann Paul, PhD, MD · Max Delbrück Center - Charite University, Berlin, Germany

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-03-01
Primary Completion
2027-04-30
Completion
2027-04-30

Countries

  • Czechia
  • Germany

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06280755 on ClinicalTrials.gov