Centro Hospitalar de Vila Nova de Gaia / Espinho E.P.E

1 results · Page 1 of 1

Swipe the table sideways for more columns.

Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Pyruvate Kinase Deficiency Global Longitudinal Registry	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, anemia, congenital nonspherocytic hemolytic anemia, familial hemolytic anemia, hematologic disorder, hemolytic anemia, hereditary disease, pyruvate kinase deficiency of red cells	Active, not recruiting	Not stated	2026-09-28		NCT03481738

Clinical trials