Managing Transient Neurologic Episodes in Surgery for Moyamoya Disease

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

88 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-05-21

Study Completion Date

2027-03-31

Brief Summary

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The goal of this study is to study the incidence of post-operative Transient Neurologic Events (TNEs) within 30 days postoperatively, as assessed by clinical neurological scales, binned by week. Collect data on all interventions and assessments performed during the recovery post surgery up to 30 days, to understand what factors might cause Transient Neurologic Events (TNEs) and determine how these can be reduced in Moyamoya subjects post surgery.

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Detailed Description

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Conditions

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Moya Moya Disease

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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MoyaMoya Subjects

Subjects will receive standard of care moyamoya surgical intervention and be followed for 30 days post for transient neurological episodes (TNEs).

Standard of Care

Intervention Type OTHER

Standard of care treatment of Transient Neurologic Events (TNEs) as needed

Interventions

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Standard of Care

Standard of care treatment of Transient Neurologic Events (TNEs) as needed

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Moyamoya Disease (MMD) patients undergoing direct extracranial-intracranial (ECIC) bypass. Patients above the age of 3 years old are eligible for the study