Clinical trial Recruiting at 1 site Observational Ages 18 to 65

Observing brain networks in moyamoya disease patients under anesthesia

Official title: Functional Magnetic Resonance-Based Observations of Brain Networks and Cerebrovascular Reactivity in Patients With Moyamoya Disease Under Anesthetic Sedation, A Prospective Observational Cohort Study

Run by Beijing Tiantan Hospital · NCT06041659 · Data updated 2026-11-12

This study looks at how brain blood flow and activity change in patients with moyamoya disease while they are under anesthesia to help improve their care during surgery.

Quick facts

Study typeObservational
Ages18 Years to 65 Years
SexAll
Enrollment48 (estimated)
SponsorBeijing Tiantan Hospital
Academic / other
Locations1 site (Beijing, Beijing Municipality)
StatusRecruiting
StartedOctober 24, 2023
Main results expectedDecember 31, 2025
Study endsDecember 31, 2025
Registry record updatedFebruary 13, 2025
Trial IDNCT06041659 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 18-65 with moyamoya disease scheduled for revascularization surgery.

Probably not a fit

Patients with severe preoperative conditions, such as significant cerebral infarction or those unable to cooperate with the examination, may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study focuses on patients with moyamoya disease who are scheduled for revascularization surgery. It utilizes functional Magnetic Resonance Imaging (fMRI) to assess changes in cerebral blood flow, oxygen metabolism, and network connectivity during anesthesia. The aim is to understand how these factors influence neurological functions post-surgery, which is crucial for effective perioperative management. By monitoring these parameters, the study seeks to enhance the understanding of cerebral dynamics in patients with compromised vascular networks.

Why it matters

Potential benefit: If successful, this study could lead to improved perioperative management strategies that minimize neurological impairments in moyamoya disease patients.

How similar studies have gone: While fMRI has been used in various cerebrovascular diseases, this specific application in moyamoya disease under anesthesia is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients with moyamoya disease scheduled for direct or indirect intracranial and extracranial revascularization surgery
* Age between 18-65 years
* Obtain written informed consent.

Exclusion Criteria:

* 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

Where it's running

  • Beijing Tiantan Hospital, Capital Medical University
    Beijing, Beijing Municipality, China
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.