Polycythemia, primary familial and congenital
Polycythemia, primary familial and congenital
Explore linked clinical trials. Standard reference: MESH:M05313032 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Molecular Biology of Polycythemia and Thrombocytosis | Hemic and Lymphatic Diseases, Hypoxia, Myeloproliferative Disorders, Pathological Conditions, Signs and Symptoms, Polycythemia, primary familial and congenital, Signs and Symptoms, Signs and Symptoms, Respiratory, blood platelet disease, bone marrow disorder, hematologic disorder, polycythemia, thrombocytosis disease | Recruiting | Not stated | 2026-03-09 | NCT00722527 | |
| EVAluation of Erythrocytosis PRospEctive Cohort STudy | Erythrocytosis, Hemic and Lymphatic Diseases, Myeloproliferative Disorders, Neoplasms by Site, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Polycythemia, primary familial and congenital, acquired polycythemia vera, bone marrow disorder, bone marrow neoplasm, disease, hematologic disorder, hematopoietic and lymphoid system neoplasm, neoplasm, polycythemia | Not yet recruiting | Not stated | 2025-01-21 | NCT06785870 |