Neurocognitive and Radiological Assessments in Adult Moyamoya Undergoing Surgery (NRAAMUS)
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About
Adult patients with moyamoya disease (MMD) are reported to suffer from considerable impairment of executive function/attention. Although reduced cerebrovascular reserve (CVR) in frontal areas has been detected by perfusion MRI and then confirmed to be associated with executive dysfunction in adult MMD, the structural and functional changes is still unclear with progression of executive dysfunction. Furthermore, it is very important to study the association between the neurocognitive and radiological improvement after surgical revascularization, so as to help detecting cerebral regions which are involved in executive deterioration or improvement after surgery. Then the investigators can determine whether these regions can be used as indicators to decide rational therapeutic schedule and timing of adult MMD with executive dysfunction.
Thus the aim of this study is to primarily find out the neuropsychological and radiological correlates in adult MMD, and then to quantitatively evaluate the effectiveness of surgical revascularization in prevention of executive dysfunction in adult MMD.
Full description
Previous studies of adult moyamoya disease (MMD) have revealed that vascular cognitive impairment (VCI) is the consequence of ischemic damage to dynamic factors such as cerebral hypoperfusion, rather than to cerebral gray matter. However, it is still unclear which regions are affected by MMD and how these regions respond to the progressive cognitive decline. In other way, the investigators need to detect spatial patterns in the brain activity of MMD in order to understand its pathophysiological nature.
Surgical revascularization has been accepted as the only effective form of treatment in preventing future ischemic episodes. However, its effectiveness in cognitive protection is still unknown. Thus, the investigators determine to quantitatively evaluate cognitive and radiological outcomes in adult MMD postoperatively and during follow-ups.
Enrollment
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Inclusion criteria
- Right-handed Chinese people aged over 18 years
- No evidence of recent or remote infarct in the cerebral cortical, basal ganglia, brainstem or cerebellum
- No evidence of recent or remote intracerebral hemorrhage
- Diagnosis confirmed by digital subtraction angiography (DSA) according to Suzuki scale
- No surgical intervention before recruitment
- Physically capable of cognitive testing
- Geographically accessible and reliable for follow-up.
Exclusion criteria
- Significant neurological diseases or psychiatric disorders that could affect cognition
- Other cerebrovascular diseases (such as atherosclerosis or vasculitides) likely to cause focal cerebral ischemia
- Concomitant cerebrovascular diseases (such as aneurysms or arteriovenous malformation) that need surgical intervention
- Severe systemic diseases
- Pregnant or perinatal stage women
- Any diseases likely to death within 2 yeas
- Taking drugs such as benzodiazepine clonazepam
- Any contraindications or allergy to aspirin
- Allergy to iodine or radiographic contrast media
- Past history of surgical revascularization
- Concurrent participation in any other experimental treatment trial
- Any condition that in the surgeon's judgment suggests the patient an unsuitable surgical candidate.
Trial design
Primary purpose
Allocation
Interventional model
Masking
80 participants in 2 patient groups
Trial contacts and locations
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Central trial contact
Yuxiang Gu, MD,PhD; Yu Lei, MD
Data sourced from clinicaltrials.gov
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