fetal erythroblastosis
fetal erythroblastosis
Explore linked clinical trials. Standard reference: MONDO:000676011 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Prenatal Blood Typing With Next Generation Sequencing (NGS) - an Implementation Study in HDFN (PREFAB) | fetal erythroblastosis | Not yet recruiting | Not applicable | 2026-07-20 | NCT07715214 | |
| Uncovering the Etiologies of Non-immune Hydrops Fetalis | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Edema, Female Urogenital Diseases and Pregnancy Complications, 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 | Enrolling by invitation | Not applicable | 2026-04-17 | NCT05528796 | |
| 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 | |
| Fetal Electrophysiologic Abnormalities in High-Risk Pregnancies Associated With Fetal Demise | Arrhythmias, Cardiac, Brugada syndrome, Cardiac Conduction System Disease, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Death, Death, Sudden, Edema, Female Urogenital Diseases and Pregnancy Complications, Fetal Death, Fetal Diseases, Hemic and Lymphatic Diseases, Hernia, Hernia, Abdominal, Infant Death, Infant, Newborn, Diseases, Musculoskeletal Abnormalities, Pathologic Processes, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Sudden Infant Death, Urogenital Diseases, alpha thalassemia spectrum, anemia, cardiovascular disorder, congenital heart disease, fetal erythroblastosis, gastroschisis, heart disorder, hematologic disorder, hereditary disease, hydrops fetalis, immune system disorder, inherited hemoglobinopathy, musculoskeletal system disorder, neonatal anemia, pregnancy disorder, pregnancy disorder with abortive outcome, thalassemia, twin to twin transfusion syndrome | Recruiting | Not stated | 2026-03-04 | NCT03775954 | |
| Application of Quantitative Hemorrhage Detection in Fetomaternal Hemorrhage Syndrome for the Diagnosis of Hemolytic Disease of the Newborn | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases and Pregnancy Complications, Fetal Diseases, Hemic and Lymphatic Diseases, Infant, Newborn, Diseases, Urogenital Diseases, fetal erythroblastosis, hematologic disorder, immune system disorder, pregnancy disorder | Not yet recruiting | Not stated | 2026-02-24 | NCT07371520 | |
| Reliability of Transcutaneous Bilirubin Measurement According to the Skin Colour of Newborns | Brain Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, Hyperbilirubinemia, Neonatal, Infant, Newborn, Diseases, Jaundice, Neonatal, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, bilirubin encephalopathy, brain disorder, central nervous system disorder, fetal erythroblastosis, hematologic disorder, hyperbilirubinemia, immune system disorder, metabolic disease, nervous system disorder | Not yet recruiting | Not stated | 2026-01-02 | NCT07315126 | |
| Bilirubin Neurotoxicity (BN) and Neurodevelopmental Impairment (NDI) in Extremely Preterm (EP) Infants: Avoidable by Reducing the Usual Intravenous Lipid (UL) Administration | Brain Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Infant, Newborn, Diseases, Nutritional and Metabolic Diseases, Obstetric Labor Complications, Obstetric Labor, Premature, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Premature Birth, Urogenital Diseases, bilirubin encephalopathy, brain disorder, central nervous system disorder, fetal erythroblastosis, hematologic disorder, hyperbilirubinemia, immune system disorder, metabolic disease, nervous system disorder, pregnancy disorder | Active, not recruiting | Phase 2 | 2025-11-28 | NCT04584983 | |
| Risk Factors and Clinical Outcomes of Neonatal Anemia in NICU | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases and Pregnancy Complications, Fetal Diseases, Hemic and Lymphatic Diseases, Infant, Newborn, Diseases, Infections, Inflammation, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Sepsis, Systemic Inflammatory Response Syndrome, Urogenital Diseases, fetal erythroblastosis, hematologic disorder, immune system disorder, pregnancy disorder | Not yet recruiting | Not stated | 2025-09-23 | NCT07188298 | |
| Cord Blood S100B Protein Levels in Neonates Following Intrauterine Transfusions for HDFN-Associated Fetal Anemia | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases and Pregnancy Complications, Fetal Diseases, Hemic and Lymphatic Diseases, Hypoxia, Hypoxia, Brain, Infant, Newborn, Diseases, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Signs and Symptoms, Respiratory, Urogenital Diseases, brain disorder, brain hypoxia - ischemia, brain ischemia, cardiovascular disorder, central nervous system disorder, cerebrovascular disorder, fetal erythroblastosis, hematologic disorder, immune system disorder, nervous system disorder, pregnancy disorder, vascular disorder | Recruiting | Not stated | 2025-05-22 | NCT06984445 | |
| Safe Threshold to Discontinue Phototherapy in Hemolytic Disease of Newborn | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases and Pregnancy Complications, Fetal Diseases, Hemic and Lymphatic Diseases, Hemolysis, Hyperbilirubinemia, Neonatal, Infant, Newborn, Diseases, Jaundice, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Skin Manifestations, Urogenital Diseases, fetal erythroblastosis, hematologic disorder, hyperbilirubinemia, immune system disorder, pregnancy disorder | Recruiting | Not applicable | 2025-01-03 | NCT04218318 | |
| In-utero Hematopoietic Stem Cell Transplantation for the Treatment of Fetuses With Bart's Hydrops Fetalis Syndrome | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Edema, Female Urogenital Diseases and Pregnancy Complications, 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 | Recruiting | Not applicable | 2023-04-12 | NCT05797272 |