New registry to track dengue risks in bleeding disorder patients
NCT ID NCT07409857
First seen Feb 15, 2026 · Last updated Apr 29, 2026 · Updated 14 times
Summary
This study creates a registry to collect data on dengue infections in people with congenital bleeding disorders like hemophilia. It aims to understand how often severe bleeding occurs, what treatments are needed, and survival rates. The study includes both past cases (from 2015) and new cases, involving up to 100 participants worldwide.
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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: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Ramathibodi Hospital
RECRUITINGBangkok, Thailand
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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