New registry aims to unlock secrets of myasthenia gravis
NCT ID NCT03792659
First seen Jan 06, 2026 · Last updated Jun 20, 2026 · Updated 30 times
Summary
This study is building a registry of 800 adults with myasthenia gravis at Yale University. Participants will donate blood and stool samples, which will be used for future research. No new treatments are being tested—the goal is to collect data to help scientists better understand the disease.
Disclaimer
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This is a summary of
the original study
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Yale-New Haven Hospital
RECRUITINGNew Haven, Connecticut, 06510, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
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What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
What this could lead to
If successful, this registry could provide valuable data for future studies on myasthenia gravis, potentially leading to better understanding or treatments.
What could go wrong
This is an observational registry, not a treatment trial. It does not test any therapy, so it cannot directly improve patient health.
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.