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
Qualifiers
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 design
Treatments tested in this trial
- Standard of Care
Treatment groups
88 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov