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Correlation study between ambient temperature and acute onset of multiple sclerosis

Correlation study between ambient temperature and acute onset of multiple sclerosis

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300070290
Enrollment
Unknown
Registered
2023-04-07
Start date
2023-04-20
Completion date
Unknown
Last updated
2023-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

nervous system autoimmune diseases

Interventions

MS patients:none
Patients with neuromyelitis optica spectrum disease and other central demyelinating diseases:none
healthy control:none

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 65 Years

Inclusion criteria

Inclusion criteria: MS Patient Group 1. Chinese citizens of both sexes aged 14 to 65 years old; 2. The diagnosis of multiple sclerosis (MS) should be made in the neuroimmunology specialist clinic of Huashan Hospital. Two or more experienced specialists are recommended to make the diagnosis of MS independently, excluding other possible diseases; 3. The diagnostic criteria referred to the 2010 McDonald standard; 4. Agree receiving venous blood collection and follow-up; 5. Understand and sign informed consent; Control group 1 (patients with other central demyelinating disorders such as neuromyelitis optica spectrum disorders) 1. Chinese citizens of both sexes aged 14 to 65 years old; 2. The diagnosis of neuromyelitis optica spectrum disorder (NMOSD) and other central demyelinating diseases should be performed in the neuroimmunology specialist clinic of Huashan Hospital. Two or more experienced specialists are recommended to make the diagnosis of NMOSD independently, excluding other possible diseases; 3. The diagnostic criteria of neuromyelitis optica spectrum disorders (NMOSD) refer to the Chinese Guidelines for the diagnosis and treatment of neuromyelitis optica spectrum disorders (2021 edition); 4. The diagnostic criteria of MOG-IgG related disorders (MOGAD) refer to the Chinese expert consensus on the diagnosis and treatment of MOGAD (2020 version); 5. Understand and sign informed consent; 6. Agree receiving venous blood collection and follow-up. Control group 2 (healthy people) 1. Chinese citizens of both sexes aged 14 to 65 years old; 2. No history of hospitalization in the past 6 months; 3. Understand and sign informed consent; 4. Able to cooperate with the completion of venous blood collection and follow-up.

Exclusion criteria

Exclusion criteria: MS Patient Group 1. Patients with pregnancy; 2. Have joined other clinical investigators in the past 3 months; 3. Patients whose diagnosis of multiple sclerosis (MS) is not considered by two or more experts; 4. AQP4-IgG, MOG-IgG and other known demyelinating disease-related antibodies positive; 5. Patients who have contraindications to blood collection or cannot accept blood collection; 6. Patients with definite infection (including latent infection) and malignant tumors; 7. History of mental illness or substance abuse; 8. Other conditions deemed ineligible for inclusion by the investigators. Control group 1 (patients with other central demyelinating disorders such as neuromyelitis optica spectrum disorders) 1. Patients with pregnancy; 2. Have joined other clinical investigators in the past 3 months; 3. Patients who have contraindications to blood collection or cannot accept blood collection; 4. Patients with definite infection (including latent infection) and malignant tumors; 5. History of mental illness or substance abuse; 6. Other conditions considered by the investigators to be ineligible for inclusion. Control group 2 (healthy people) 1. Patients with pregnancy; 2. Have joined other clinical investigators in the past 3 months; 3. Patients who have contraindications to blood collection or cannot accept blood collection; 4. Patients with definite infection (including latent infection) and malignant tumors; 5. History of mental illness or substance abuse; 6. Other conditions considered by the investigators to be ineligible for inclusion.

Design outcomes

Primary

MeasureTime frame
Heat shock protein 90;

Secondary

MeasureTime frame
Cytokines like interleukin-1, interleukin-6, tumor necrosis factor-a, etc.;The distribution of immune cell subsets (such as Th1, Th2, Th17, Treg cells);

Countries

China

Contacts

Public ContactChen Xiangjun

Huashan Hospital, Fudan University

xiaoniliu13@fudan.edu.cn+86 18221382327

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026