Clinical Research Details
Multiple Sclerosis Patient Registry
- Samia Khoury
- Yehya El Kouzi
- Wassim Assaad
Conditions and Keywords
Eligibility and IRB
The MS patient registry aims:
To collect long-term clinical information from a large group of patients with MS or a single episode of symptoms suggestive of MS.
To enable researchers to prospectively evaluate long term treatment effects of current and future disease modifying therapies in standard clinical practice.
To enable researchers to document disease outcomes
Patients with MS or related CNS demyelinating disorders presenting to the MS center
Signed informed consent