Managing Transient Neurologic Episodes in Surgery for Moyamoya Disease
ConditionMoya Moya Disease
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age3+
SponsorStanford University
About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Moyamoya Disease (MMD) patients undergoing direct extracranial-intracranial (ECIC) bypass. Patients above the age of 3 years old are eligible for the study
Disqualifiers
Renal dysfunction, electrolyte disturbances neuromuscular disorders including Myaesthenia Gravis, heart block
Trial population
Moyamoya subject undergoing a standard of care direct and indirect extracranial-intracranial (ECIC) bypass.
Trial design
Design model
Cohort
Time perspective
Retrospective
Treatments tested in this trial
Standard of Care
Other interventionStandard of care treatment of Transient Neurologic Events (TNEs) as needed
Treatment groups
88 Participants
are divided into 1 treatment groupGroup A: MoyaMoya Subjects1 intervention
Trial outcomes
Primary outcomes
1
Transient Neurologic Events (TNEs)
Number of Incidence of post-operative Transient Neurologic Events (TNEs) within 30 days postoperatively, as assessed by clinical neurological scales (e.g., NIH Stroke Scale, Modified Rankin Scale), binned by week.
Time frame
30 days post-surgerySponsors and contacts
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Source ClinicalTrials.gov