Actively Recruiting

Age: 3Years +
All Genders
ID06880341

MagNETs- Managing Transient Neurologic Episodes in Surgery for Moyamoya Disease

Led by Stanford University · Updated on 2025-05-28

88

Participants Needed

1

Research Sites

12 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the occurrence of post-operative Transient Neurologic Events (TNEs) within 30 days after surgery in people with Moyamoya Disease. The goal is to understand the causes of these events and find ways to reduce them during recovery after surgery. This observational study is sponsored by Stanford University and focuses on patients undergoing Moyamoya surgical treatment. Participants will receive the standard surgical care for Moyamoya Disease involving direct extracranial-intracranial bypass. After surgery, they will be monitored for 30 days to identify any transient neurological episodes. All interventions and assessments performed during this recovery period will be recorded to gather detailed information about factors that might contribute to TNEs. During the study, participants will undergo clinical neurological evaluations and other assessments as part of their routine care to track any TNEs. Researchers will collect data on neurological symptoms weekly during the 30 days post-surgery. The main outcome measured is the incidence of TNEs within this period. Participants will be followed closely to ensure accurate data collection and safety throughout the study duration.

CONDITIONS

Brief Title

Managing Transient Neurologic Episodes in Surgery for Moyamoya Disease

Who Can Participate

Age: 3Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Moyamoya Disease patients undergoing direct extracranial-intracranial (ECIC) bypass surgery
  • Age 3 years and older
Not Eligible

You will not qualify if you...

  • Renal dysfunction
  • Electrolyte disturbances
  • Neuromuscular disorders including Myasthenia Gravis
  • Heart block

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Surgery day plus initial hospital stay

Participants undergo standard of care moyamoya surgical intervention and immediate post-operative care.

1 surgical visit and hospital stay

Post-operative Follow-up

Duration - 30 days post-surgery

Participants are monitored for transient neurologic episodes (TNEs) during the 30 days following surgery.

Follow-up visits as part of routine care

Trial Site Locations

Total: 1 location

1

Stanford University Hospital

Palo Alto, California, United States, 94305

Actively Recruiting

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Research Team

J

Jinendra Ekanayake

A

Anthony Bet

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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