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Acupuncture as a disease modifying therapy for the treatment in remission stage of neuromyelitis optics spectrum disorders

Acupuncture as a disease modifying therapy for treatment in remission stage of neuromyelitis optics spectrum disorders: a prospective clinical randomised parallel trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN92125844
Enrollment
40
Registered
2016-12-22
Start date
2016-04-01
Completion date
Unknown
Last updated
2017-02-06

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

Conditions

Neuromyelitis optics spectrum disorders of remitting stage Nervous System Diseases Neuromyelitis optics spectrum disorders of remitting stage

Interventions

Participants are randomised to one of two groups using a computerised random number table. Intervention group: Participants are treated with oral azathioprine at a dose of 2mg/Kg-D for three months i

Sponsors

Beijing Traditional Chinese Medical Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Diagnosis of neuromyelitis optics spectrum disorders in accordance with NMOSDs diagnostic criteria established by the international panel for NMO diagnosis (IPND) in 2015. 2. In remission stage (no acute progress, no corticosteroid therapy or immunoglobulin therapy, plasma exchange, stable condition without relapse signs) 3. Age of 18-75 years old 4. EDSS score less than 5 5. No other treatment with immunosuppressive drugs within 6 months or no other immunosuppressive drugs other than azathioprine 6. Provision of informed consent

Exclusion criteria

Exclusion criteria: 1. Oral azathioprine intolerant patients 2. History of severe allergies 3. Those who can not tolerate acupuncture 4. Clinically significant history of disease, blood disease, endocrine, metabolism, liver, lung, urinary system, nervous system, skin disease, other major primary disease and psychiatric disease 5. Malignant tumor 6. B type hepatitis 7. Pregnancy or lactation

Design outcomes

Primary

MeasureTime frame
Disability is measured using the Expanded disability scale score at baseline, 3, 6 and 12 months.

Secondary

MeasureTime frame
1. AQP4-IgG level is measured using cell transfection method at baseline and 3 months 2. Annual relapse rate is measured using computer formula at baseline, 3, 6 and 12 months

Countries

China

Contacts

Public ContactChunchen Wang

Outcome results

None listed

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