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RecruitingNCT07781579Updated Aug 24, 2026

5T MRI and Metabolomics-Based Hemorrhage Risk Prediction in Moyamoya Disease

An observational study in Moyamoya Disease, Intracranial Hemorrhages and Stroke, sponsored by Beijing Hospital. Recruiting at 1 site in China. Per ClinicalTrials.gov, last updated 2026-08-24.

Sponsored by Beijing Hospital · Observational

From the registry’s dates

  • Started Feb 2026; still recruiting 9 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
500
Sex
All
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Study 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.

Read the detailed description

BACKGROUND MMD is a rare cerebrovascular disease characterized by stenosis or occlusion of the distal internal carotid artery bifurcation and the formation of collateral networks at the base of the brain. In China, the annual incidence is approximately 1.14 per 100,000 population and has been rising. MMD presents with ischemic or hemorrhagic manifestations; hemorrhagic-type MMD has an annual hemorrhage rate of approximately 17% and a mortality of 6.8%-20%, with a worse prognosis than the ischemic type. Autopsy and imaging studies indicate that dilatation and rupture of fragile, thin-walled collateral vessels are the principal cause of MMD hemorrhage. Hemodynamic changes and vessel wall alterations are associated with hemorrhage risk, but conventional 1.5T/3.0T MRA lacks the spatial resolution and signal-to-noise ratio required to quantify collateral vessels. 5.0T MRI offers substantially improved signal-to-noise ratio; its TOF-MRA quality is comparable to 7.0T and superior to 3.0T, enabling precise multidimensional assessment of collateral vessel morphology, blood flow, and vessel wall features. Meanwhile, metabolomic studies have consistently identified metabolic alterations (amino acid, lipid, purine/pyrimidine pathways) in patients with MMD, and the investigators' preliminary work has shown that glycine metabolism promotes angiogenesis and is associated with collateral vessel formation. However, the association between metabolomic alterations and the hemorrhagic subtype, and whether metabolic changes can serve as early biomarkers of hemorrhagic MMD, remains unknown.

STUDY DESIGN This is a single-center, prospective, observational cohort study conducted at Beijing Hospital. Patients with MMD or moyamoya syndrome confirmed by DSA who meet the eligibility criteria will be consecutively enrolled. Based on the initial presentation, participants will be classified into a hemorrhagic-type group and an ischemic-type group. All participants will undergo routine preoperative multimodal imaging (CT, CTA/P, MRA, DSA), a preoperative 5.0T MRI examination, and preoperative blood and urine sampling. Participants will be followed for 12 months; new-onset intracranial hemorrhage, analyzed per cerebral hemisphere, is the endpoint event, adjudicated by clinical symptoms and confirmatory head CT or MRI.

5T MRI ACQUISITION All MRI examinations will be performed on a 5T whole-body MR scanner (Siemens Healthcare, Erlangen, Germany) with a birdcage transmit and 32-channel receive head coil (Nova Medical, MA, USA). Sequences include T1W MPRAGE, optimized whole-brain isotropic TOF-MRA (0.40 mm isotropic resolution), an optimized single-slab TOF-MRA covering the middle cerebral artery and basal ganglia region (0.23×0.23×0.36 mm³), HR-VWI, and 3D ASL, together with conventional DWI/T2WI/SWI. Image quality will be graded before inclusion in the dataset.

IMAGING ANALYSIS A deep learning pipeline will be developed for quantitative collateral assessment: a VT-UNet 3D segmentation network will extract the vascular skeleton from TOF-MRA, followed by feature extraction with a Swin Transformer architecture. The skeleton will be converted to a tetrahedral mesh for computational hemodynamics, deriving wall shear stress (WSS), wall shear stress gradient (WSSG), oscillatory shear index (OSI), and relative residence time (RTT). Vessel wall features (stenosis site, remodeling pattern, stenosis degree, lumen area, wall thickness, remodeling index) will be manually annotated on HR-VWI by two independent readers (ICC > 0.8 required) and quantified with PyRadiomics (approximately 1,790 radiomic features). Brain perfusion and structural parameters (cerebral blood flow, cortical thickness, cortical surface area, brain and deep nuclei volumes) will be derived from 3D ASL and T1WI.

METABOLOMICS Preoperative venous blood (5 mL; plasma separated within 20 minutes) and urine (10 mL) will be collected and stored at -80 °C. High-throughput metabolomic profiling of these samples, including amino acid metabolites, will be performed to identify novel biomarkers of hemorrhagic MMD. STA specimens trimmed during direct bypass surgery will be formalin-fixed, paraffin-embedded, and analyzed by immunohistochemistry to cross-validate biomarkers and explore mechanisms.

MODEL DEVELOPMENT AND VALIDATION Clinical baseline data, 5T MRI features, hemodynamic parameters, and metabolomic biomarkers will be integrated. Feature selection and dimensionality reduction will use L1 regularization; baseline machine learning models (logistic regression, naive Bayes, SVM, neural network, KNN, decision tree) will be tested and, if necessary, ensemble learning methods will be applied, with hyperparameters tuned by grid search. Internal validation will use five repetitions of five-fold cross-validation; external validation will be performed in the validation cohort. The primary performance metric is the area under the receiver operating characteristic curve (AUROC), with accuracy, recall, precision, and F1 score as secondary metrics. The final model will be used to construct a hemorrhage risk stratification system.

SAMPLE SIZE Based on an annual hemorrhage rate of 17% and an estimated 5 predictor variables (10 events per variable), 50 hemorrhage events are required, yielding approximately 294 participants; adjusted for a 10% loss to follow-up and a 7:3 training/validation split, 500 participants will be enrolled.

SIGNIFICANCE This study will enable hemorrhage risk stratification of patients with MMD, early identification of high-risk individuals, and timely surgical revascularization, thereby reducing the disability and mortality of MMD and informing the comprehensive prevention and treatment of stroke.

02

Conditions studied

  • Moyamoya Disease
  • Intracranial Hemorrhages
  • Stroke

Keywords

  • Moyamoya disease
  • Hemorrhage risk prediction
  • 5T MRI
  • Metabolomics
  • Deep learning
  • Collateral vessels
  • Machine learning
  • Prediction model
03

In context

Moyamoya Disease

62 studies on the registry are indexed under Moyamoya Disease; 30 are open to participants now.

This study's planned enrollment of 500 is above the median of 300 across 29 observational studies indexed under Moyamoya Disease.

Browse Moyamoya Disease studies →

Lead sponsor

Beijing Hospital is the lead sponsor of 51 studies on the registry; 23 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Patients with moyamoya disease or moyamoya syndrome confirmed by digital subtraction angiography (DSA) at the Department of Neurosurgery, Beijing Hospital, who meet the eligibility criteria and provide written informed consent. Participants are classified into a hemorrhagic-type group and an ischemic-type group according to their initial clinical presentation.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Moyamoya disease or moyamoya syndrome confirmed by digital subtraction angiography (DSA).
  • Able to undergo a 5.0T magnetic resonance imaging (MRI) examination.

Exclusion criteria

Exclusion Criteria:

  • Claustrophobia or any other condition precluding completion of imaging acquisition.
  • Previous revascularization surgery in both cerebral hemispheres.
  • Any intracranial hemorrhage event within 1 month before enrollment.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
500 participants (estimated)
Patient registry
No

Groups and cohorts

  • 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.

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What researchers measure

Primary outcomes

  1. New-onset intracranial hemorrhage within 12 months

    Analyzed per cerebral hemisphere. Hemorrhage events are adjudicated based on the participant's symptoms and confirmed by head CT or MRI. The time and location of each event are recorded. Participants who undergo rev

    Time frame: Time Frame: 12 months after enrollment

Secondary outcomes

  1. Discriminative performance of the hemorrhage risk prediction model

    Area under the receiver operating characteristic curve (AUROC) of the integrated 5T MRI and metabolomics-based hemorrhage risk prediction model in the validation cohort, with 5×5-fold cross-validation for internal validation.

    Time frame: At model validation (Year 2)

07

Study locations

1 of 1 sites recruiting
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References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: Undecided

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Feb 2026 (actual). Primary completion is estimated for Dec 2027, 22 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 16, 2026
First posted
Aug 24, 2026
StartActual
Feb 1, 2026
Primary completionEst.
Dec 31, 2027
CompletionEst.
Dec 31, 2027
Last update
Aug 24, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07781579
Lead sponsor
Beijing Hospital
Responsible party
Sponsor
First posted
Aug 24, 2026
Start date
Feb 1, 2026
Primary completion
Dec 31, 2027 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Aug 24, 2026

Study contacts

Shaosen Zhang, MD
Contact
longyoubafang@hotmail.com
+86 18611284839

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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