Plain-English translation of NCT07415824 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Read our Multiple Sclerosis research guide →The Multiple Sclerosis Implementation Network (MSIN) is creating a large patient database by collecting medical records and information from people with MS. Researchers, doctors, and patient leaders are working together to use this data to find better ways to care for MS patients and improve their quality of life. By joining, you'd be helping scientists learn what works best in real-world MS treatment.
Many people with MS struggle to get consistent, high-quality care across different doctors and hospitals. This registry exists to bring together real-world health information so that researchers can discover what treatments and care approaches work best, and help doctors provide better care to all MS patients.
You likely qualify if…
You likely don't qualify if…
As a participant, you would allow the research team to access and store your medical records from your healthcare providers in a secure database. You may be asked to complete surveys about your health and quality of life. The study is ongoing, so your participation can continue over time as researchers use the data to improve MS care.
AI-generated summary from trial data · Jun 19, 2026 · Not medical advice
United States
Sponsor
The University of Texas Health Science Center, Houston
Collaborators
Novartis, Multiple Sclerosis Association of America
Enrollment target
~2,000 participants
Started
April 2025
Primary completion
December 2030
Age range
18 Years and older
Last updated on clinicaltrials.gov in February 2026.
Reach out to the team running this trial. Response times vary — some teams are faster than others.
Central contact
Amanda Montague, EdM
Multiple Sclerosis Association of America
Tell us you're interested and we'll help connect you with the research team. We'll walk you through what to expect first — no email needed to get started.