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The application of molecular imaging for the assessment of neuroinflammation in patients with NMOSD and MOG-AD

The application of molecular imaging for the assessment of neuroinflammation in patients with NMOSD and MOG-AD

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200066921
Enrollment
Unknown
Registered
2022-12-21
Start date
2022-05-20
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Neuromyelitis Optica Spectrum Disorders and Myelin oligodendrocyte glycoprotein antibody disease

Interventions

Gold Standard:Antibody test

Sponsors

Renji Hospital, School of Medicine, Shanghai Jiao Tong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria of NMOSD patients: (1) Age: 18-75; (2) Conformed diagnosis (according to 2015 NMOSD international consensus), and the AQP4 antibody test positive; (3) During the acute stage of the disease, and within 30 days from this attack to PET/MR; (4) EDSS score = 8; (5) Normal liver and kidney function, blood test, urine routine test and other biochemical tests; (6) Able to complete follow-up; (7) Intracranial lesions exist according to MRI examination or symptoms and signs; (8) The patient or families signs the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Allergy of related imaging agents; (2) Diagnosed diseases of the central nervous system that lead to epilepsy, cognitive impairment or abnormal mental symptoms, including Alzheimer's disease, Parkinson's disease, central nervous system tumors, schizophrenia, etc; (3) Lactating or pregnant women in 5 years; (4) History of brain surgery; (5) Patients with serious medical diseases (such as heart, liver, lung and kidney insufficiency); (6) Patients with abnormal expression or disturbance of consciousness, unstable vital signs, and unable to cooperate with the examination due to severe mental and behavioral abnormalities, central respiratory failure, etc; (7) The researchers believe that the subjects may not be able to complete the study or may not be able to comply with the requirements of the study;

Design outcomes

Primary

MeasureTime frame
SUV of FDG;

Secondary

MeasureTime frame
SUV of FDG;SUV of Acetate;Sensitivity;Specificity;

Countries

China

Contacts

Public ContactYangtai Guan
yangtaiguan@sina.com+86 21 68383482

Outcome results

None listed

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