- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07537504
Language Function Reorganization in Patients With Arteriovenous Malformations
April 16, 2026 updated by: Beijing Tiantan Hospital
Study on the Language Function Reorganization in Right CerebralHemisphere of Patients With Brain Arteriovenous Malformations Using Multimodal MRI
Brain arteriovenous malformation (AVM) is generally considered as a congenital lesion.
Its unique clinical manifestation is that when the unruptured AVM involves and destroys the language function area of the left hemisphere, the patient has almost no language disorder.
This phenomenon is distinct from those of acquired diseases such as cerebral infarction and gliomas.
There is a hypothesis that it might be associated with that the occurrence of AVM is earlier than period of language learning.
Therefore, patients with AVMs involving language areas can be regarded as population whose language areas are congenital "knocked out" but the language functions remain normal, which provide a special model and new insights for language reorganization research.
Previous studies have found that the right hemisphere plays an important role in the remodeling of language function in patients with AVMs, but the specific mechanism remains unclear.
The purpose of this study is to further elaborate the role of the right cerebral hemisphere in the reorganized language network and the interhemispheric interaction mechanisms in patients with AVMs involving the language areas, using multimodal magnetic resonanceimaging and from multiple dimensions such as functional remodeling, white matter pathway remodeling, structural remodeling, etc., so as to further understand the remodeling mechanism of the Chinese language network after damage of language areas, and also to provide a theoretical basis for the protection of language function in brain network surgery.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
120
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Xiaofeng Deng, MD
- Phone Number: +8613426341444
- Email: windmessenger@126.com
Study Contact Backup
- Name: Zekun Han, MM
- Phone Number: +8613523485634
- Email: ZKHan0810@163.com
Study Locations
-
-
-
Beijing, China
- No. 119 South 4th Ring West Road, Fengtai District, Beijing 100070, China
-
Contact:
- Xiaofeng Deng, MD
- Phone Number: +8613426341444
- Email: windmessenger@126.com
-
Contact:
- Zekun Han, MM
- Phone Number: +8613523485634
- Email: ZKHan0810@163.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Healthy Control and AVM patients
Description
Inclusion Criteria:
- AVM located within left-hemisphere language regions
- right-handedness
- native Mandarin Chinese speakers
- age 18-60 years
- high school education or above
Exclusion Criteria:
- comorbid neurological or psychiatric disorders
- AVM-related intracranial hemorrhage within the past month
- prior AVM treatment
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy Control
|
All participants underwent MRI scans
|
|
AVM patients
|
All participants underwent MRI scans
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Structural MRI (sMRI) Primary Metric
Time Frame: baseline and three months after surgery
|
Cortical thickness of bilateral language-related brain regions (measured via FreeSurfer); intergroup differences between AVM patients and healthy controls
|
baseline and three months after surgery
|
|
Functional MRI Secondary Metrics
Time Frame: baseline and three months after surgery
|
Resting-state regional brain activity: Amplitude of Low Frequency Fluctuation (ALFF) and Regional Homogeneity (ReHo) Dynamic effective connectivity (DCM): Excitatory/inhibitory effective connectivity between lesioned left hemisphere and remodeled right hemisphere regions
|
baseline and three months after surgery
|
|
Diffusion MRI (dMRI) Primary Metrics
Time Frame: baseline and three months after surgery
|
White matter microstructural integrity: Fractional Anisotropy (FA, DTI) and Neurite Density Index (NDI, NODDI) of language-related white matter tracts Corpus callosum diffusion metrics (FA, NDI) reflecting interhemispheric communication
|
baseline and three months after surgery
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Multimodal Combined & Exploratory Metrics
Time Frame: baseline and three months after surgery
|
Function-structure coupling: Correlation analysis between fMRI LI, cortical thickness, and white matter FA/NDI Track-weighted dynamic functional connectivity (TW-dFC): White matter tract-mediated dynamic functional interactions Graph theory brain network analysis: Global efficiency, local efficiency, nodal degree, and modularity of the language network Subgroup comparative metrics: Neuroimaging differences between right-hemisphere remodelers and non-remodelers Correlation between imaging metrics and basic demographic/clinical variables (age, lesion location)
|
baseline and three months after surgery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Xiaofeng Deng, Brijing Tiantan Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
April 20, 2026
Primary Completion (Estimated)
December 31, 2027
Study Completion (Estimated)
December 31, 2027
Study Registration Dates
First Submitted
April 10, 2026
First Submitted That Met QC Criteria
April 16, 2026
First Posted (Actual)
April 17, 2026
Study Record Updates
Last Update Posted (Actual)
April 17, 2026
Last Update Submitted That Met QC Criteria
April 16, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KY2025-104-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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