Managing Transient Neurologic Episodes in Surgery for Moyamoya Disease
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Standard of Care.
- Who it may be relevant to
- Registry conditions: Moya Moya Disease. Basic parameters: from 3 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
MagNETs- Managing Transient Neurologic Episodes in Surgery for Moyamoya Disease
Overview
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.
Interventions
- Other Standard of Care
Standard of care treatment of Transient Neurologic Events (TNEs) as needed
Primary outcome measures
- Transient Neurologic Events (TNEs) [Time frame: 30 days post-surgery]
Eligibility criteria
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
Exclusion criteria
- Renal dysfunction, electrolyte disturbances neuromuscular disorders including Myaesthenia Gravis, heart block
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
United States · 1 center
- Stanford University Hospital — Palo Alto
Identifiers
NCT: NCT06880341 · 77828