Actively Recruiting

Age: 18Years - 60Years
All Genders
NCT06817434

Study on Evaluating the Effectiveness of Statins in the Treatment of Moyamoya Disease

Led by Beijing Tiantan Hospital · Updated on 2025-02-10

330

Participants Needed

1

Research Sites

106 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to investigate the effectiveness of statins in the treatment of moyamoya disease based on multimodal magnetic resonance imaging.

CONDITIONS

Official Title

Study on Evaluating the Effectiveness of Statins in the Treatment of Moyamoya Disease

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • The imaging examination meets the diagnostic criteria for moyamoya disease
  • Signed informed consent form
  • Age 18 years or older
  • Baseline modified Rankin Scale (mRS) score 2 points or less
  • Patient receives revascularization or conservative treatment
  • At least one imaging follow-up result available
Not Eligible

You will not qualify if you...

  • Patients with atherosclerosis, autoimmune diseases, meningitis, Down syndrome, cranial trauma, or previous radioactive head irradiation (causing secondary cerebrovascular disease or moyamoya syndrome)
  • Individuals under 18 years old
  • Refusal to participate in the study
  • Pregnant patients
  • Presence of intracranial aneurysms, cerebrovascular malformations, brain tumors, or hydrocephalus
  • History of stroke more than three months before moyamoya disease diagnosis
  • History of coronary heart disease or prior cardiovascular/cerebrovascular surgeries (including cerebral revascularization, stent implantations, endarterectomy, coronary artery bypass grafting)
  • Allergy to contrast media
  • Missing or poor quality imaging data
  • Refusal or inability to undergo imaging follow-up
  • Receiving other types of lipid-lowering drug treatments

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Beijing Tiantan Hospital

Beijing, China, China, 100070

Actively Recruiting

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Research Team

Q

Qian Zhang

CONTACT

C

Chaofan Zeng

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

0

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