Rare heart disease data hunt could speed up future treatments
NCT ID NCT07344480
First seen Jan 17, 2026 · Last updated May 15, 2026 · Updated 18 times
Summary
This study gathers medical and genetic information from 100 children with a rare genetic condition called RASopathy that causes severe heart thickening. The goal is to create a detailed dataset that can be used as a comparison group in future drug trials. No new treatments are tested; instead, researchers hope to better understand the disease and help design faster, more effective studies for new medicines.
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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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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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TUM Klinikum Deutsches Herzzentrum München
RECRUITINGMünchen, 80636, Germany
Conditions
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