Scientists investigate skin repair in rare blistering disease
NCT ID NCT01874769
First seen Mar 21, 2026 · Last updated Apr 29, 2026 · Updated 4 times
Summary
This study looked at skin cells from 30 people with recessive dystrophic epidermolysis bullosa (RDEB), a rare genetic condition that causes severe blistering. Researchers measured how well skin cells called keratinocytes and fibroblasts can grow and repair wounds. The goal was to better understand the disease, not to test a new treatment.
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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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Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
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Genom att skicka in godkänner du våra Användarvillkor
Locations
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Guy's and ST Thomas NHS Foundation trust/Guy's Hospital
London, SE19RT, United Kingdom
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Inserm U781 Service de Génétique Necker Hospital for sick children
Paris, 75743/ Cedex 15, France
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Service de dermatologie Necker Hospital for sick children
Paris, 75743 Cedex 15, France
Conditions
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