Moyamoya Disease Clinical Trials

Find Moyamoya Disease Clinical Trials Near You

Development and Validation of a Hemorrhage Risk Prediction Model for Moyamoya Disease Based on 5T MRI and Metabolomic Features: A Prospective Cohort Study

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Intracranial hemorrhage is a leading cause of death and disability in patients with moyamoya disease (MMD), yet clinically available tools for predicting long-term hemorrhage risk are lacking. Dilatation and rupture of fragile collateral vessels are considered the main cause of MMD-related hemorrhage; however, conventional 1.5T/3.0T MRI cannot adequately quantify collateral vessel morphology, blood flow, and vessel wall features. Metabolomic alterations have been implicated in MMD pathogenesis, including angiogenesis and collateral vessel formation. This prospective cohort study will consecutively enroll patients with MMD or moyamoya syndrome confirmed by digital subtraction angiography (DSA) at Beijing Hospital. All participants will undergo preoperative 5.0T brain MRI, including time-of-flight MR angiography (TOF-MRA), 4D MRA, high-resolution vessel wall imaging (HR-VWI), 3D arterial spin labeling (ASL), and conventional sequences (T1WI, DWI, T2WI, SWI). Preoperative blood and urine samples will be collected for metabolomic profiling, and superficial temporal artery (STA) specimens trimmed during direct bypass surgery will be retained for immunohistochemical cross-validation. Using deep learning (VT-UNet for collateral vessel segmentation and Swin Transformer for feature extraction) combined with machine learning methods, the investigators will develop and validate an integrated hemorrhage risk prediction model that combines 5T MRI features, hemodynamic parameters, metabolomic biomarkers, and clinical baseline data. Participants will be followed for 12 months; new-onset intracranial hemorrhage, analyzed per cerebral hemisphere, will be the endpoint event. The study aims to (1) establish a hemorrhage risk stratification system for early identification of high-risk patients to guide timely surgical revascularization, and (2) identify core metabolomic and imaging biomarkers of MMD-related hemorrhage.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: t
View:

• Moyamoya disease or moyamoya syndrome confirmed by digital subtraction angiography (DSA).

• Able to undergo a 5.0T magnetic resonance imaging (MRI) examination.

Locations
Other Locations
China
Beijing Hospital
RECRUITING
Beijing
Contact Information
Primary
Shaosen Zhang, MD
longyoubafang@hotmail.com
+86 18611284839
Time Frame
Start Date: 2026-02-01
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 500
Treatments
Hemorrhagic-type MMD group
Patients whose initial clinical manifestation is intracranial hemorrhage. All participants receive preoperative 5.0T MRI, blood and urine collection for metabolomics, and routine clinical assessment, followed for 12 months for new-onset hemorrhage (per cerebral hemisphere).
Ischemic-type MMD group
Patients whose initial clinical manifestation is ischemic stroke, transient ischemic attack, or incidental asymptomatic findings. Assessments and follow-up are identical to the hemorrhagic-type group, with new-onset hemorrhage (per cerebral hemisphere) as the endpoint event.
Related Therapeutic Areas
Sponsors
Leads: Beijing Hospital

This content was sourced from clinicaltrials.gov