National, Multicentric Registry Study on Neuroimmunological Diseases in China
About This Trial
The aim of this study is to establish a real-world clinical neuroimmune disease research cohort, to follow up and observe the prognosis of patients with different subtypes and subgroups, and to provide support for the treatment, early warning, and outcome prediction research of neuroimmune diseases.
Who May Be Eligible (Plain English)
Original Eligibility Criteria
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Treatments Being Tested
Data collection and follow-up observation
At the time of enrollment, the patient's biological samples are collected to obtain genetic information. Following enrollment, trained investigators carry out a 2-year follow-up observation through face-to-face, telephone call or online visits. During the follow-up, basic clinical information, laboratory tests, imaging examinations, neurophysiology, clinical classification, medication use, and scale assessments are collected.
Data collection
Collect demographic and genetic information from healthy volunteers upon enrollment.