Neuromyelitis Optica Spectrum Disorders
Conditions
Brief summary
Neuromyelitis Optica (NMO)/ Neuromyelitis Optica Spectrum Disorders (NMOSD) is an immune-mediated inflammatory demyelinating disease of the central nervous system mainly involving optic nerve and spinal cord. It is clinically characterized by simultaneous or sequential involvement of the optic nerve and spinal cord, presenting a progressive or remission and relapse course, which can lead to paralysis and blindness. The objective of this study is to provide evidence regarding treat effects and factors related to prognosis which will help physicians better evaluable risk-benefit in NMOSD management and improve patients' outcome.
Detailed description
Neuromyelitis Optica (NMO)/ Neuromyelitis Optica Spectrum Disorders (NMOSD) is an immune-mediated inflammatory demyelinating disease of the central nervous system mainly involving optic nerve and spinal cord. It is clinically characterized by simultaneous or sequential involvement of the optic nerve and spinal cord, presenting a progressive or remission and relapse course, which can lead to paralysis and blindness. Globally, there is no solid data available for the diagnosis, treatment and prognosis of patients with acute Neuromyelitis Optica Spectrum Disorders (NMOSD) attack, particularly very rare data from prospective studies. This is a multicenter, prospective, real-world cohort study in patients with acute NMOSD attack in China. Baseline data for approximately 200 patients with acute NMOSD attack from approximately 4 centers will be collected. Patients with acute NMOSD attack (including first episodes and relapses) whose expansile disability status score (EDSS ) ≥ 2 points at baseline will be eligible to be further included in prospective study cohort for analysis of treatment effects and prognosis. The objective of this study is to provide evidence regarding treat effects and factors related to prognosis which will help physicians better evaluable risk-benefit in NMOSD management and improve patients' outcome.
Interventions
None listed
Sponsors
Nanfang Hospital, Southern Medical University
Second Affiliated Hospital of Guangzhou Medical University
Guangdong 999 Brain Hospital
Third Affiliated Hospital, Sun Yat-Sen University
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1\. Inclusion criteria for patients with baseline data collection: 1. The subject can fully understand the content of the study and voluntarily sign the informed consent form; 2. Male or female ≥18 years old; 3. Diagnosed as NMOSD based on 2015 NMOSD diagnostic criteria of International NMO Diagnostic Team (IPND) and currently under acute attack. 2\. Inclusion criteria for subjects enrolled in a prospective study cohort should further meet: 1. The subject can fully understand the content of the study and voluntarily sign the informed consent form; 2. Male or female,≥18 years old; 3. Diagnosed as NMOSD based on 2015 NMOSD diagnostic criteria of International NMO Diagnostic Team (IPND) and currently under acute attack. 4. Subjects with acute attack (including first episodes and relapse) should have an EDSS of ≥ 2 at baseline; and for patients with acute relapse, new symptoms or the primary symptoms, being judged by investigator, should have been aggravated for 24 hours or more \[11-13\]; 5. The subject should have typical symptoms of movement, sensation, vision, defecation/urination or nausea/vomiting at attack; 6. Subjects should agree to participate in the study, and to receive AQP4-IgG examination before and after treatment; 7. Subjects should agree to undergo an ophthalmologic examination before and after treatment; 8. Subjects should agree to participate the study and agree to have the collected data analyzed by this study. 3\.
Exclusion criteria
1. Subjects treated with study medication in another clinical trial during the last 30 days or 5 half-life periods prior to screening or during the effect period of the drug, whichever is the longest; Note: Subjects who participated in an observational study (ie, the study did not require changes to medication or other interventions) were not excluded. 2. Immediate relatives of the researcher/research center staff directly related to the study, or the researcher/research center staff directly related to the study (immediate relatives refer to spouses, parents, children or siblings (Whether it's biological or legal adoption).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Expansile Disability Status Score | at the end of the first high-dose intravenous Methylprednisone (IVMP) therapy (up to 3 weeks )among subjects who received high-dose IVMP | Compared with baseline, changes in EDSS（Expansile Disability Status Score ）at the end of the first high-dose intravenous Methylprednisone (IVMP) therapy among subjects who received high-dose IVMP. EDSS score is based on the evaluation of eight functional systems of the central nervous system.The total score of the assessment is between 0 and 10 points, and each 0.5 is divided into one grade, which is divided into 20 grades. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Expansile Disability Status Score | at discharge (7 days after last treatment) | Compared with baseline, proportion of subjects with EDSS improved ≥1 point at discharge (7 days after last treatment) |
| Changes In AQP4-IgG | at the end of the first IVMP therapy（up to 3 weeks) among subjects who received high-dose IVMP | Compared with baseline , changes in AQP4-IgG at the end of the first IVMP therapy among subjects who received high-dose IVMP |
| As Assessed By Snellen Chart | at the end of the first high-dose IVMP theraty (up to 3 weeks) among subjects who received high-dose IVMP | Compared with baseline , changes in visual acuity (as assessed by Snellen chart) at the end of the first high-dose IVMP therapy among subjects who received high-dose IVMP |
| PGI-I Score | at the end of the first high-dose IVMP therapy(up to 3 weeks) among subjects who received high-dose IVMP | Score of Patient Global Improvement-Impression (PGI-I) at the end of the first high-dose IVMP therapy among subjects who received high-dose IVMP Patient Global Impressions (PGI)-Improvement Mark the box that best describes how you (the patient) have felt in general since you started taking this medicine. (Choose one) 1 = Very assessed, 2 = Much better, 3 = A little better, 4 = The same, 5 = A little worse, 6 = Much worse, 7 = Very much worse |
| The proportion of patients who did not respond to the first high-dose IVMP therapy(up to 3 weeks) | at discharge (7 days after the last treatment) | The proportion of patients who did not respond to the first high-dose IVMP therapy(up to 3 weeks) |
Countries
China
Outcome results
None listed