RecruitingNCT06817434
Study on Evaluating the Effectiveness of Statins in the Treatment of Moyamoya Disease
Sponsor
Beijing Tiantan Hospital
Enrollment
330 participants
Start Date
Dec 15, 2024
Study Type
OBSERVATIONAL
Conditions
Summary
The purpose of this study is to investigate the effectiveness of statins in the treatment of moyamoya disease based on multimodal magnetic resonance imaging.
Eligibility
Min Age: 18 YearsMax Age: 60 Years
Inclusion Criteria6
- The imaging examination meets the diagnostic criteria for moyamoya disease;
- Sign the informed consent form;
- Age ≥18 years old;
- Baseline mRS score ≤2 points;
- The patient receives revascularization/conservative treatment;
- There is at least 1 imaging follow-up result.
Exclusion Criteria11
- Patients with atherosclerosis, autoimmune diseases, meningitis, Down syndrome, cranial trauma, or those who have undergone radioactive head irradiation, as these conditions may lead to secondary cerebrovascular disease and contribute to the development of Moyamoya syndrome;
- Individuals under the age of 18;
- Participants who refuse to take part in this study;
- Pregnant patients;
- Those with concurrent intracranial aneurysms, cerebrovascular malformations, brain tumors, or hydrocephalus;
- A history of stroke occurring more than three months prior to the diagnosis of Moyamoya disease;
- Individuals with a history of coronary heart disease or previous cardiovascular and cerebrovascular surgical interventions, including cerebral revascularization, intracranial artery stent implantation, carotid artery stenting, endarterectomy, coronary artery bypass grafting, or coronary stent implantation;
- Allergies to contrast media;
- Patients with missing imaging data or whose image quality cannot be analyzed;
- Individuals who refuse or are unable to undergo imaging follow-up;
- Patients receiving other types of lipid-lowering drug treatments.
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Interventions
DRUGRevascularization/Conservative management
Revascularization/Conservative management
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06817434
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