Study asks: how do kids live after surviving a rare birth defect?
NCT ID NCT07432672
Summary
This study aimed to understand the day-to-day quality of life for children who survived surgery for a rare birth defect called congenital diaphragmatic hernia (CDH). Researchers surveyed 80 children (ages 5-18), their parents, and siblings using a standard questionnaire to measure physical, emotional, and social well-being. The goal was to gather information to help doctors provide better long-term care for these survivors.
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Contacts and locations
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Locations
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Medical University of Vienna
Vienna, Vienna, 1090, Austria
Conditions
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