Actively Recruiting
Functional Magnetic Resonance-Based Observations of Brain Networks and Cerebrovascular Reactivity in Patients With Moyamoya Disease Under Anesthetic Sedation, A Prospective Observational Cohort Study
Led by Beijing Tiantan Hospital · Updated on 2025-02-13
48
Participants Needed
1
Research Sites
N/A
Total Duration
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AI-Summary
What this Trial Is About
Moyamoya disease is a condition where the blood vessels at the base of the brain narrow progressively, leading to poor blood flow and the formation of abnormal vascular networks. This study focuses on adult patients with moyamoya disease undergoing surgery and aims to observe how brain blood flow, oxygen use, and brain network connectivity change under anesthesia. The goal is to better understand anesthesia management to help protect brain function and improve cognitive abilities during the surgical period. Participants in this observational study are adults with moyamoya disease scheduled for specific brain revascularization surgeries. The study uses functional Magnetic Resonance Imaging (fMRI) to evaluate cerebrovascular reserve and brain network connectivity before sedation, after sedation, and while maintaining controlled blood pressure. No experimental treatments are given; instead, brain function changes are monitored during the perioperative period. During the study, participants undergo brain scans and electroencephalogram monitoring at multiple time points around the surgery. Researchers will measure changes in brain functional networks and track postoperative delirium up to five days after surgery. The study observes how anesthesia and blood pressure management affect brain oxygen metabolism and connectivity. Participation lasts through the surgical and immediate recovery period, providing insights into brain function under anesthesia in moyamoya disease.
CONDITIONS
Brief Title
Functional Magnetic Resonance-Based Observations of Brain Networks in Moyamoya Disease Patients Under Anesthesia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with moyamoya disease scheduled for direct or indirect intracranial and extracranial revascularization surgery
- Age between 18-65 years
- Obtain written informed consent.
You will not qualify if you...
- Patients with preoperative claustrophobia, sensory or motor aphasia that are unable to understand and cooperate with the examination
- Preoperative cranial imaging suggesting cerebral infarction lesion diameter >15mm
- Patients allergic to anesthetic drugs
- Metal implants in the body
- Undergoing other experimental drug or instrumentation trials
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery
Participants undergo brain MRI and electroencephalogram assessments before sedation, after sedation, and after maintaining blood pressure at baseline levels.
1 visit (in-person)
Duration - Day of surgery
Participants receive direct or indirect intracranial and extracranial revascularization surgery under anesthetic sedation.
1 visit (in-person)
Duration - 5 days
Participants are monitored for postoperative delirium and recovery during the first five days after surgery.
Daily visits for 5 days (in-person)
Trial Site Locations
Total: 1 location
1
Beijing Tiantan Hospital, Capital Medical University
Beijing, Beijing Municipality, China, 100070
Actively Recruiting
Research Team
S
Shu Li
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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