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A multicenter prospective cohort study on the natural history of moyamoya disease development

A multicenter prospective cohort study on the natural history of moyamoya disease development

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400081954
Enrollment
Unknown
Registered
2024-03-18
Start date
2024-03-18
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

Moyamoya disease

Interventions

Divide into positive group and negative group based on whether there is any progression of the disease during the natural course of the disease (occurrence of stroke):None

Sponsors

Beijing Tiantan Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with moyamoya disease by DSA or MRA or CTA meet the diagnostic criteria of the 2014 Japanese Guidelines for Moyamoya Disease; 2. Patients with moyamoya disease under conservative observation and without revascularization history; 3. Adult patients with moyamoya disease aged =18 and =70 years; 4. No previous cerebral infarction, cerebral hemorrhage, no history of dementia or major mental illness as proved by imaging; 5. Know, agree and sign informed consent;

Exclusion criteria

Exclusion criteria: 1. During follow-up, DSA, MRA and CTA were suspected to be non-moyamoya disease patients, and vascular diseases caused by immune system diseases; 2. Patients who cannot complete the annual follow-up review; 3. Patients with other major diseases, such as blood system diseases, leukemia, tumors, etc., who are receiving treatment that will affect the test results (such as long-term chemotherapy, radiotherapy); 4. Those who do not understand or sign informed consent; 5. Those who have contraindications for magnetic resonance examination (those with pacemakers, nerve stimulators, artificial metal heart valves and other metal foreign bodies, etc.) or cannot cooperate with the completion of image collection.

Design outcomes

Primary

MeasureTime frame
MRI;

Secondary

MeasureTime frame
Brain cognitive function test;

Countries

China

Contacts

Public ContactRong Wang

Beijing Tiantan Hospital Affiliated to Capital Medical University

ronger090614@ccmu.edu.cn+86 130 0119 0333

Outcome results

None listed

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