Hydrops: Diagnosing & Redefining Outcomes With Precision Study
Hydrops: Diagnosing & Redefining Outcomes With Precision Study
Active, not recruiting · NCT03412760 · Registry updated 2026-04-17Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Hydrops: Diagnosing & Redefining Outcomes With Precision Study | Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Edema, Female Urogenital Diseases and Pregnancy Complications, Fetal Anomalies, Fetal Diseases, Hemic and Lymphatic Diseases, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Urogenital Diseases, alpha thalassemia spectrum, fetal erythroblastosis, hematologic disorder, hereditary disease, hydrops fetalis, immune system disorder, inherited hemoglobinopathy, pregnancy disorder, thalassemia | Active, not recruiting | Not applicable | 2026-04-17 | NCT03412760 |
4 results · Page 1 of 1
Organizations
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1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| University of California, San Francisco | San Francisco | United States | 294 |