Long-term outcomes of conservative management in moyamoya disease patients and their relatives
Official title: Long-term Outcomes of Conservative Management in Patients with Moyamoya Disease and Their First-degree Relatives
Run by Beijing Tiantan Hospital · NCT05332756 · Data updated 2026-11-12
This study looks at how well non-surgical treatments work for people with moyamoya disease and their family members over time.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 2 Years to 60 Years |
| Sex | All |
| Enrollment | 400 (estimated) |
| Sponsor | Beijing Tiantan Hospital Academic / other |
| Locations | 1 site (Beijing, Beijing Municipality) |
| Status | Recruiting |
| Started | May 1, 2022 |
| Main results expected | November 30, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | December 19, 2024 |
| Trial ID | NCT05332756 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include individuals aged 2-60 years with a clinical diagnosis of moyamoya disease who are receiving conservative management.
✕Probably not a fit
Patients with concomitant diseases or conditions that could interfere with the study outcomes may not benefit from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study investigates the long-term outcomes of conservative management in patients diagnosed with moyamoya disease and their first-degree relatives. Moyamoya disease is a chronic cerebrovascular condition characterized by the narrowing of the internal carotid arteries and the formation of abnormal blood vessels. The study aims to understand the effectiveness of conservative treatment options and explore the potential genetic and environmental factors contributing to the disease's pathogenesis. Participants will be monitored over time to assess their health outcomes and any manifestations in their relatives.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the long-term management of moyamoya disease, potentially improving patient care and outcomes.
How similar studies have gone: While there have been studies on moyamoya disease, the specific focus on long-term conservative management outcomes in both patients and their relatives is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patients with age between 2-60 years; 2. A clinical diagnosis of moyamoya disease, including unilateral and bilateral disease. 3. Patients are medically treated with antiplatelets, antiepileptics, antihypertensives and vasodilators depending on the presentation. 4. Capable of understanding the purpose and risk of the study and has signed the informed consent. If the participant is not capable of this at the time of enrollment, a legally authorized representative will provide written informed consent in accordance with all regulations. 5. Ability to comply with study follow-up. Exclusion Criteria: 1. Concomitant other diseases, including systemic vasculitis, neurofibroma, meningitis, sickle cell disease, down's syndrome, and previous basilar radiotherapy. 2. Patients with cardiogenic embolism, including a history of atrial fibrillation, valvular disease or cardiac valve replacement. 3. Patients are allergic to the contrast agents. 4. Patients are treated with direct, indirect, or combined revascularization depending on the presentation. 5. Physical or subjective failure to cooperate with the examination or serious comorbid diseases. 6. Patients are unable or unlikely to return for follow-up visits. 7. Any other reasons that, in the opinion of the investigators, make the participant unsuitable for enrollment.
Where it's running
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Beijing Tiantan Hospital Capital Medical University
Beijing, Beijing Municipality, China Recruiting
Study contacts
- Study coordinator: Qian Zhang, MD
- Email: zhangqianchina@yahoo.com
- Phone: 8613120012579
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Risk prediction for stroke and cognitive decline in Moyamoya disease and Moyamoya syndrome
A large multicenter study tests whether combining clinical data, imaging, lab and genetic information can predict who will have stroke or cognitive decline among people with Moyamoya.
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5T MRI and Metabolomics to Predict Hemorrhage Risk in Moyamoya Disease
This study tests whether advanced 5T MRI imaging and metabolomics can help predict which moyamoya patients are at higher risk of intracranial hemorrhage.
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XR-assisted CT-guided localization for EC-IC bypass in Moyamoya and chronic cerebral ischemia
The study tests whether a metaverse-based surgical simulation with extended reality helps localize vessels during EC-IC bypass for moyamoya disease or chronic cerebral ischemia.
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Family screening and early detection for moyamoya disease
This project will try to find biological signs and 5T high-resolution MRI features that could detect moyamoya earlier in people with the disease, their first-degree relatives, and people without a family history.
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Remimazolam: target-controlled infusion versus manual infusion during cerebrovascular bypass
This trial will test whether target-controlled infusion uses less remimazolam than manual infusion in adults undergoing cerebrovascular bypass surgery for moyamoya disease.
-
Cardiac index–guided blood flow management during pediatric Moyamoya EDAS surgery
This study will test whether using each child's cardiac index to guide fluids and hemodynamic care during EDAS lowers postoperative transient ischemic episodes in children with Moyamoya disease.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.