Major study launches to unravel mysteries of rare gallbladder disease
NCT ID NCT05961826
Summary
This study aims to better understand LPAC syndrome, a rare form of gallbladder disease. Researchers will follow 650 people with the condition for five years to document their symptoms, how they are diagnosed, what treatments they receive, and how the disease affects their quality of life. The goal is to gather detailed information to improve future care for people with this condition.
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Contacts and locations
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Locations
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Centre Hospitalier Annecy Genevois
Annecy, France
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Centre Hospitalier Intercommunal Aix-Pertuis
Aix-en-Provence, France
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Centre Hospitalier Intercommunal de Créteil
Créteil, France
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Centre Hospitalier Sud Francilien
Corbeil-Essonnes, France
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Centre hospitalier régional d'Orléans
Orléans, France
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Hôpital Avicenne
Bobigny, France
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Hôpital Beaujon
Clichy, France
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Hôpital Charles Nicolle
Rouen, France
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Hôpital Civil
Strasbourg, France
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Hôpital Claude Huriez
Lille, France
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Hôpital Côte de Nacre
Caen, France
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Hôpital François Mitterrand
Dijon, France
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Hôpital Haut-Lévêque
Bordeaux, France
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Hôpital Jean Bernard
Poitiers, France
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Hôpital Michallon
Grenoble, France
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Hôpital Paul Brousse
Villejuif, France
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Hôpital Rangueil
Toulouse, France
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Hôpital Robert Debré
Reims, France
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Hôpital Saint Camille
Bry-sur-Marne, France
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Hôpital Saint-Antoine
Paris, France
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Hôpital de la Croix-Rousse
Lyon, France
Conditions
Explore the condition pages connected to this study.