Nemours
Nemours
Wilmington, Delaware, United States2 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Rhizomelic Chondrodysplasia Punctata Registry | Bone Diseases, Developmental, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Peroxisomal Disorders, bone disorder, chondrodysplasia punctata, hereditary disease, inborn errors of metabolism, metabolic disease, musculoskeletal system disorder, osteochondrodysplasia, rhizomelic chondrodysplasia punctata, rhizomelic chondrodysplasia punctata type 1, rhizomelic chondrodysplasia punctata type 2, rhizomelic chondrodysplasia punctata type 3, rhizomelic chondrodysplasia punctata type 5 | Recruiting | Not stated | 2026-08-07 | NCT04569162 | |
| Primordial Dwarfism Registry | DNA ligase IV deficiency, Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies, Lowry-Wood syndrome, Meier-Gorlin syndrome, Roifman syndrome, Seckel syndrome 1, microcephalic osteodysplastic dysplasia, Saul-Wilson type, microcephalic osteodysplastic primordial dwarfism type II | Recruiting | Not stated | 2025-10-01 | NCT04569149 |