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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Childhood-onset Lupus Nephritis Initial Glucocorticoid-dose Harmonization Trial (LIGHT Trial)Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Skin and Connective Tissue Diseases, Urogenital Diseases, autoimmune disease, connective tissue disorder, glomerulonephritis, immune system disorder, kidney disorder, lupus nephritis, nephritis, systemic lupus erythematosus, urinary system disorderRecruitingPhase 42026-07-22NCT07719140
Long-term Follow-up Study of BRL-101 for TDTCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, anemia, beta thalassemia, familial hemolytic anemia, hematologic disorder, hemolytic anemia, hereditary disease, inherited hemoglobinopathy, thalassemiaRecruitingNot stated2026-07-21NCT06298630
Safety and Efficacy Evaluation of BRL-101 in Subjects With Transfusion-Dependent β-ThalassemiaCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, anemia, beta thalassemia, familial hemolytic anemia, hematologic disorder, hemolytic anemia, hereditary disease, inherited hemoglobinopathy, thalassemiaActive, not recruitingPhase 1 / Phase 22026-07-21NCT05577312
Fecal Microbiota Transplantation in Children With ASDautism spectrum disorder, neurodevelopmental disorder, pervasive developmental disorder, psychiatric disorderRecruitingNot applicable2026-06-09NCT07381374
Capizzi Escalating Methotrexate Versus High Dose Methotrexate in Children With Newly Diagnosed T-cell Lymphoblastic Lymphoma (T-LBL)T-cell Lymphoblastic LymphomaRecruitingPhase 32026-03-19NCT05681260
CCCG-ALCL-2020 for Chinese Children and Adolescents With Newly Diagnosed High-risk ALCLHemic and Lymphatic Diseases, Neoplasms by Histologic Type, T-cell non-Hodgkin lymphoma, anaplastic large cell lymphoma, immune system disorder, immunoproliferative disorder, lymphatic system disorder, lymphoma, lymphoproliferative syndrome, neoplasmActive, not recruitingPhase 32026-03-19NCT04881838
Clinical Implementation of the Group Standard for Enteral Feeding Care in Critically Ill ChildrenClinical Implementation; Enteral Nutrition; Standardized Tube Feeding CareNot yet recruitingNot applicable2026-03-02NCT07441746
Pediatric Intravenous Contrast-Enhanced Ultrasound(CEUS) in ChinaAbdominal Injuries, Abdominal Neoplasms, Ascites, Neoplasms by Site, Pathologic Processes, Pathological Conditions, Signs and Symptoms, injury, neoplasmRecruitingNot stated2025-12-08NCT07113808
Evidence-based Practice in the Management of Gastric Tube Placement in ChildrenEnteral Nutrition Therapy; Hospitalized Children; NursingRecruitingNot applicable2025-09-10NCT07038538
Investigation of Tetralogy of Fallot in NeonatesCardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Ventricular Outflow Obstruction, cardiovascular disorder, congenital heart disease, double outlet right ventricle, heart disorder, heart septal defect, heart valve disorder, pulmonary valve stenosis, pulmonic stenosis, tetralogy of fallot, transposition of the great arteries, ventricular septal defectRecruitingNot applicable2025-09-10NCT06822400
Risk Model for Metastasis Detection of NeuroblastomaNeoplasms by Histologic Type, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, Neuroectodermal Tumors, Primitive, Neuroectodermal Tumors, Primitive, Peripheral, epithelial neoplasm, neoplasm, neuroblastoma, neuroepithelial neoplasm, primitive neuroectodermal tumorEnrolling by invitationNot stated2025-05-15NCT06703944
The Effectiveness and Safety of Resective Epilepsy Surgery for TRECongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Malformations of Cortical Development, Group I, Neoplasms, Multiple Primary, brain disorder, central nervous system disorder, central nervous system malformation, cerebral cortical dysplasia, epilepsy, hamartoma, hereditary disease, hereditary neoplastic syndrome, inherited neurodegenerative disorder, neoplasm, nervous system disorder, neurocutaneous syndrome, neurodegenerative disease, tuberous sclerosisActive, not recruitingNot stated2025-01-17NCT04198181
Observational Study of Pediatric Rheumatic and Immunologic Diseases in China: The CAPRID RegistrySjogren syndrome, Skin and Connective Tissue Diseases, Stomatognathic Diseases, Xerostomia, arthritic joint disease, arthropathy, autoimmune disease, cardiovascular disorder, connective tissue disorder, dermatomyositis, diffuse scleroderma, dry eye syndrome, eye disorder, immune system disorder, juvenile idiopathic arthritis, lacrimal apparatus disorder, mouth disorder, muscle tissue disorder, musculoskeletal system disorder, myositis disease, nervous system disorder, neuromuscular disease, polymyositis, rheumatic disorder, rheumatoid arthritis, salivary gland disorder, skin disorder, systemic lupus erythematosus, systemic sclerosis, vascular disorder, vasculitisRecruitingNot stated2024-05-16NCT06417502
Belimumab After Rituximab in Resistant Primary Juvenile SSHemic and Lymphatic Diseases, Neoplasms by Histologic Type, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Sjogren syndrome, Skin and Connective Tissue Diseases, Stomatognathic Diseases, Xerostomia, arthritic joint disease, arthropathy, autoimmune disease, childhood acute lymphoblastic leukemia, connective tissue disorder, dry eye syndrome, eye disorder, hematologic disorder, immune system disorder, immunoproliferative disorder, lacrimal apparatus disorder, leukemia, lymphatic system disorder, lymphoid leukemia, lymphoproliferative syndrome, mouth disorder, musculoskeletal system disorder, neoplasm, rheumatic disorder, rheumatoid arthritis, salivary gland disorderRecruitingPhase 42024-05-16NCT06410833
Registry Study on Cystic Fibrosis in Chinese ChildrenCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Infant, Newborn, Diseases, cystic fibrosis, hereditary disease, lung disorder, pancreas disorder, respiratory system disorderNot yet recruitingNot stated2016-04-28NCT02753374
Registry Study on Primary Ciliary Dyskinesia in Chinese ChildrenAbnormalities, Multiple, Ciliopathies, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, hereditary disease, otorhinolaryngologic disease, primary ciliary dyskinesia, respiratory system disorderNot yet recruitingNot stated2016-03-10NCT02704455