2 completed. .
Follow Elliptocytosis, Hereditary: new trials by email Literature Review of Elliptocytosis, Hereditary trials Research Report on Elliptocytosis, Hereditary
Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.
| Trial | Phase | Status | Sponsor | Enrollment | Start | Updated |
|---|---|---|---|---|---|---|
| ERN-EuroBloodNet Registry on Patients With Rare Red Blood Cell Defects and COVID-19 Non applicable, is a patient registry - Hemoglobinopathies, Sickle Cell Disease | Completed | Hospital Universitari Vall d'Hebron Research Institute | 684 | 2020-04-15 | 2025-02-18 | |
| A Novel Mutation of the Spectrin Gene Hereditary Elliptocytosis (HE), Hereditary Pyropoikilocytosis (HPP) | Completed | University of Utah | 12 | 2008-02-01 | 2009-02-19 |
Anemia (1) · Anemia, Sickle Cell (1) · Beta Thalassemia, Dominant Inclusion Body Type (1) · COVID-19 (1) · Delta-Beta Thalassemia (1) · Hemoglobin SC Disease (1) · Hemoglobinopathies (1) · Pyropoikilocytosis, Hereditary (1) · Spherocytosis, Hereditary (1) · alpha-Thalassemia (1) · beta-Thalassemia (1)
Anemia, Hemolytic (2) · Anemia, Hemolytic, Congenital (2) · Congenital, Hereditary, and Neonatal Diseases and Abnormalities (2) · Genetic Diseases, Inborn (2) · Hematologic Diseases (2) · Hemic and Lymphatic Diseases (2) · Anemia (1) · Coronaviridae Infections (1) · Coronavirus Infections (1) · Infections (1) · Lung Diseases (1) · Nidovirales Infections (1) · Pneumonia (1) · Pneumonia, Viral (1) · RNA Virus Infections (1)
Hospital Universitari Vall d'Hebron Research Institute (1) · University of Utah (1)
Spain (1) · United States (1)