17 results · Page 1 of 1

Swipe the table sideways for more columns.

TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Evaluation of Analgesia for Spine Fusion Elective Surgery in Childrenidiopathic scoliosisRecruitingPhase 32026-10-07NCT06626503
Bowel Continence Across the Lifespan in People With Spina BifidaCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Fecal Incontinence, central nervous system malformation, colonic disorder, digestive system disorder, functional colonic disease, intestinal disorder, nervous system disorder, neurogenic bowel, rectal disorder, spina bifidaRecruitingNot stated2026-09-24NCT07390318
Targeted Immunotherapy After Myeloablative TBI-Based Conditioning & AlloHCT in CAYA With High Risk T-Cell ALL & LymphomaHemic and Lymphatic Diseases, Neoplasms by Histologic Type, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Precursor T-Cell Lymphoblastic Leukemia-Lymphoma, T-cell acute lymphoblastic leukemia, hematologic disorder, immune system disorder, immunoproliferative disorder, leukemia, lymphatic system disorder, lymphoid leukemia, lymphoproliferative syndrome, neoplasmRecruitingPhase 12026-09-11NCT04972942
Personalized Perioperative Analgesia Platform (PPAP) for Pediatric Spine Fusion Surgery (sIRB)Polymerase proofreading-related adenomatous polyposisRecruitingNot applicable2026-09-10NCT05367609
A Phase 2 Study of Mutant-selective PI3Kα Inhibitor, RLY-2608, in Adults and Children With PIK3CA Related Overgrowth Spectrum and Malformations Driven by PIK3CA Mutation (The ReInspire Study)CLOVES syndrome, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, Lymphatic Abnormalities, angiomatosis, angioosteohypertrophic syndrome, cardiovascular disorder, lymphatic system disorder, megalencephaly-capillary malformation-polymicrogyria syndrome, vascular disorder, vascular malformationRecruitingPhase 22026-08-25NCT06789913
A Study of Pitolisant in Patients With Prader-Willi SyndromeAbnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disorders of Excessive Somnolence, Dyssomnias, Imprinting Disorders, Neurobehavioral Manifestations, Neurologic Manifestations, Nutritional and Metabolic Diseases, Overweight, Prader-Willi syndrome, Sleep Disorders, Intrinsic, chromosomal disorder, hereditary disease, intellectual disability, nervous system disorder, nutritional disorder, obesity disorder, overnutrition, psychiatric disorder, sleep-wake disorderRecruitingPhase 32026-08-25NCT06366464
Non-invasive Prediction of EArly Cardiac rEjectionCardiac MRI; Cell Free DNA; Heart Transplant; Pediatric Heart Transplant; RejectionRecruitingNot stated2026-08-20NCT07770659
Modeling Mortality in Duchenne Muscular Dystrophy Cardiomyopathy: Identification of Surrogate Outcome Measures for DMD Drug TrialsBecker muscular dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne muscular dystrophy, Muscular Disorders, Atrophic, X-linked disease, cardiomyopathy, cardiovascular disorder, heart disorder, hereditary disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular diseaseRecruitingNot stated2026-07-28NCT07674758
Trial of Indication-Based Transfusion of Red Blood Cells in ECMOPathologic Processes, Pathological Conditions, Signs and Symptoms, Shock, multiple organ dysfunction syndromeActive, not recruitingNot applicable2026-07-02NCT05405426
Distal Radius Interventions for Fracture TreatmentArm Injuries, Wrist Fractures, Wrist Injuries, bone fracture, injuryRecruitingNot applicable2026-07-01NCT05131685
Immunotherapy Before and After Surgery for Treatment of Recurrent or Progressive High Grade Glioma in Children and Young AdultsNeoplasms by Histologic Type, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, astrocytoma (excluding glioblastoma), epithelial neoplasm, glioblastoma, glioma, grade III glioma, malignant glioma, neoplasm, neuroepithelial neoplasm, primitive neuroectodermal tumorActive, not recruitingPhase 12026-06-15NCT04323046
Biliary Atresia Study in Infants and ChildrenCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Abnormalities, Digestive System Diseases, bile duct disorder, biliary atresia, biliary tract disorder, cholestasisRecruitingNot stated2026-06-04NCT00345553
Gastroschisis Outcomes of Delivery (GOOD) StudyCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hernia, Hernia, Abdominal, Musculoskeletal Abnormalities, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, gastroschisis, musculoskeletal system disorderRecruitingNot applicable2026-05-27NCT02774746
Comparison of Uncomplicated Candidemia Therapy Duration in ChildrenBacterial Infections and Mycoses, Infections, Invasive Fungal Infections, candidiasis, candidiasis, invasive, fungal infectious diseaseRecruitingNot applicable2026-04-17NCT05763251
Long-Term Outcomes After the Multisystem Inflammatory Syndrome in Childrenpediatric multisystem inflammatory disease, COVID-19 relatedActive, not recruitingNot stated2026-03-27NCT05287412
OMEGA: Outcome Measures in Eosinophilic Gastrointestinal Disorders Across the AgesDigestive System Diseases, Eosinophilia, Eosinophilic enteropathy, Hemic and Lymphatic Diseases, Hypersensitivity, Immediate, digestive system disorder, eosinophilic colitis, eosinophilic esophagitis, eosinophilic gastritis, eosinophilic gastroenteritis, esophageal disorder, esophagitis, gastroenteritis, hematologic disorder, immune system disorder, leukocyte disorderRecruitingNot stated2025-09-12NCT02523118
An Observational Study of Carbaglu® for the Treatment of MMA and PA in Adults and PediatricsCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Hyperammonemia, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, hereditary disease, inborn disorder of amino acid metabolism, inborn errors of metabolism, metabolic disease, methylmalonic acidemia, propionic acidemiaRecruitingNot stated2025-04-15NCT05040178