Massive online survey aims to unlock lupus mysteries
NCT ID NCT06927219
Summary
This is an online registry, not a treatment study. It aims to better understand the lives of people with lupus by collecting information about their diagnosis, symptoms, treatments, and quality of life. Up to 10,000 adults and children with lupus (or their caregivers) can participate entirely from home by completing surveys every six months. The data will be used to guide future research and improve support for the lupus community.
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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Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
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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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Online Registry - No Physical Site Required
RECRUITINGWashington D.C., District of Columbia, 20037, United States
Conditions
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