Clinical trial Recruiting at 1 site Observational Ages 2 to 60

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.

More Moyamoya Disease trials

Quick facts

Study typeObservational
Ages2 Years to 60 Years
SexAll
Enrollment400 (estimated)
SponsorBeijing Tiantan Hospital
Academic / other
Locations1 site (Beijing, Beijing Municipality)
StatusRecruiting
StartedMay 1, 2022
Main results expectedNovember 30, 2026
Study endsDecember 31, 2026
Registry record updatedDecember 19, 2024
Trial IDNCT05332756 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

  • Beijing Tiantan Hospital Capital Medical University
    Beijing, Beijing Municipality, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.