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Real-World Study on the Diagnosis and Treatment of Moyamoya Vasculopathy

Real-World Study on the Diagnosis and Treatment of Moyamoya Vasculopathy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500105704
Enrollment
Unknown
Registered
2025-07-09
Start date
2025-04-21
Completion date
Unknown
Last updated
2025-07-14

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

Conditions

Moyamoya Vasculopathy

Interventions

Sponsors

The First Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with moyamoya disease or moyamoya syndrome by imaging examination (such as cerebral angiography, etc.); 2. Age< 80 years old; 3. Patients or their legal representatives are able to understand and consent to the information collection of this study and sign an informed consent form. 4. Willing to accept follow-up by the research team.

Exclusion criteria

Exclusion criteria: 1. Refusal of the patient or his/her legal representative to participate in this study. 2. Combined with other serious neurological diseases that may affect the evaluation of the results of this study. 3. Presence of severe hepatic and renal insufficiency or other systemic diseases, which may affect the patient's survival or treatment decision. 4. Other conditions that the investigator considers the patient to be unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Pharmacotherapy group - hemorrhagic or ischemic stroke occurs;Pharmacotherapy group - neurological prognosis;Pharmacotherapy group - Deaths during 24-month follow-up;Surgical treatment group/endovascular intervention treatment group - Vascular patency status;Surgical treatment group/endovascular intervention treatment group - Onset of hemorrhagic/ischemic stroke;Surgical treatment group/endovascular intervention treatment group - death;Surgical treatment group/endovascular intervention treatment group - cerebral vascular status;

Secondary

MeasureTime frame
Pharmacotherapy group - radiographic progression;Pharmacotherapy group - quality of life and cognitive impairment;Surgical treatment group/endovascular intervention treatment group - periprocedural complication;Surgical treatment group/endovascular intervention treatment group - Neurological function;Surgical treatment group/endovascular intervention treatment group - quality of life and cognitive impairment;

Countries

China

Contacts

Public ContactLi Conghui

The First Hospital of Hebei Medical University

13363880072@163.com+86 186 3388 9708

Outcome results

None listed

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