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Clinical Trials/NCT02559089
NCT02559089
Unknown
Not Applicable

Multicenter and Prospective Clinical Registry Study of Anti-N-methyl-D-aspartate Receptor Encephalitis in China

Beijing Tongren Hospital0 sites400 target enrollmentMay 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anti-NMDA Receptor Enphalitis
Sponsor
Beijing Tongren Hospital
Enrollment
400
Primary Endpoint
death
Last Updated
10 years ago

Overview

Brief Summary

Anti-NMDA receptor encephalitis is the most common curable non-infectious autoimmune encephalitis,but because of the lack of recognition in the clinic, usually been misdiagnosed as other causes of encephalitis. Therefore, it is urgent to establish a database of anti-NMDA receptor encephalitis in Chinese population. The multi-center, prospective clinical trial of anti-NMDA receptor encephalitis in China's , combined with Beijing Xuanwu hospital, Beijing Tiantan Hospital, Beijing Children's Hospital and other hospitals around the country, by screening the NMDA receptor antibody and summarizing the cases analysis, in order to provide evidence for clinical diagnosis and treatment of anti-NMDA receptor encephalitis.

Registry
clinicaltrials.gov
Start Date
May 2015
End Date
May 2017
Last Updated
10 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Beijing Tongren Hospital
Responsible Party
Principal Investigator
Principal Investigator

Jia Wei Wang,MD

Chairman and Full Professor of Department of Neurology and Medical Research Center

Beijing Tongren Hospital

Eligibility Criteria

Inclusion Criteria

  • Older than 6 months.
  • Encephalopathy symptoms (change of mental state and consciousness level) persist for more than 24 hours;
  • At least one or more clinical features of the followings: fever, epilepsy, focal neurological deficiency symptoms, changes in CSF(cerebrospinal fluid inflammatory), changes in EEG (electroencephalogram), radiographic abnormalities;
  • Clinical suspected encephalitis, but conventional detected methods cannot make etiology clear.
  • Signed informed consent

Exclusion Criteria

  • Infants less than 6 months;
  • The metabolic encephalopathy;
  • Infectious encephalitis with clear pathogen clinically, referring the specific pathogenic microorganisms, including: bacteria, virus, fungus, parasite, spirochete and so on;
  • Non-infectious encephalitis with clear diagnosis clinically, including: multiple sclerosis, neuromyelitis optic, acute disseminated encephalomyelitis and so on.

Outcomes

Primary Outcomes

death

Time Frame: 30 days

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