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Prader-Willi syndrome (PWS) is a rare and complex genetic disease characterized by hypothalamic-pituitary axis dysfunction combining eating disorders associated with hyperphagia and satiety deficiency...
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Lead Sponsor
Assistance Publique - Hôpitaux de Paris
NCT05939453 · Prader-Willi Syndrome, Excessive Daytime Sleepiness, and more
NCT07348601 · Prader-Willi Syndrome
NCT05545306 · Obesity, Normal Physiology, and more
NCT07187830 · Chronic Kidney Disease in Type 2 Diabetes, Obesity & Overweight
NCT04453072 · Obesity, Malignant Neoplasm
Service diététique Hôpital Marin d'Hendaye- AP-HP
Hendaye
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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