Actively Recruiting
Long-term Outcomes of Conservative Management in Patients with Moyamoya Disease and Their First-degree Relatives (LAMORA)
Led by Beijing Tiantan Hospital · Updated on 2024-12-19
400
Participants Needed
1
Research Sites
243 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to investigate the long-term outcomes of conservative management in patients with moyamoya disease and their first-degree relatives, and provide potential pathogenesis of moyamoya disease.
CONDITIONS
Official Title
Long-term Outcomes of Conservative Management in Patients with Moyamoya Disease and Their First-degree Relatives (LAMORA)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 2 and 60 years
- Clinical diagnosis of moyamoya disease, including unilateral or bilateral disease
- Receiving medical treatment with antiplatelets, antiepileptics, antihypertensives, or vasodilators as needed
- Able to understand the study purpose and risks and provide informed consent (or have a legal representative provide consent)
- Able to comply with study follow-up visits
You will not qualify if you...
- Presence of other diseases such as systemic vasculitis, neurofibroma, meningitis, sickle cell disease, Down's syndrome, or previous basilar radiotherapy
- History of cardiogenic embolism including atrial fibrillation, valvular disease, or cardiac valve replacement
- Allergy to contrast agents
- Received surgical revascularization treatment
- Inability or unwillingness to cooperate with examinations or presence of serious comorbid diseases
- Unlikely or unable to return for follow-up visits
- Any other conditions that investigators consider make participation unsuitable
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Beijing Tiantan Hospital Capital Medical University
Beijing, Beijing Municipality, China
Actively Recruiting
Research Team
Q
Qian Zhang, MD
CONTACT
C
Chaofan Zeng, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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