Rare hand deformity study seeks answers from past records
NCT ID NCT07404514
First seen Feb 11, 2026 · Last updated May 24, 2026 · Updated 16 times
Summary
This study looks at existing medical records and asks parents to fill out questionnaires to better understand a rare hand condition called ulnar longitudinal deficiency. The goal is to learn how the condition changes over time and what factors guide decisions about surgery. No new tests or visits are required for participants. The findings will help doctors create better, more consistent care plans for children with this condition.
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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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Hôpitaux Paris Est Val-de-Marne - Centre de Référence des Malformations des Membres
Saint-Maurice, 94410, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
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