Great Ormond Street Hospital for Children NHS Foundation Trust
Great Ormond Street Hospital for Children NHS Foundation Trust
Explore linked clinical trials.34 results · Page 1 of 2
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Neonatal Enhanced Recovery After Surgery (ERAS) Outcomes Study | Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities | Not yet recruiting | Not stated | 2026-10-01 | NCT07771478 | |
| Children's Intensive Care Outcomes and Health Inequities: A Mixed Methods Study of Social Determinants in Paediatric Intensive Care in England | Paediatric Intensive Care | Not yet recruiting | Not stated | 2026-08-18 | NCT07771179 | |
| Pediatric Expansion Study of the Sentio System | Ear Diseases, Hearing Loss, Conductive, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, hearing disorder, hearing loss disorder, hearing loss, mixed conductive-sensorineural, nervous system disorder, otorhinolaryngologic disease | Active, not recruiting | Not applicable | 2026-08-14 | NCT06976086 | |
| Cerebellar Mutism Syndrome Study | Neoplasms by Site, Neurobehavioral Manifestations, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, brain disorder, central nervous system cancer, central nervous system disorder, communication disorder, language disorder, mutism, neoplasm, nervous system disorder, neurodevelopmental disorder, psychiatric disorder, speech disorder | Recruiting | Not stated | 2026-08-12 | NCT02300766 | |
| Metagenomics for Ocular Inflammation | Infections, eye disorder, uveal disorder, uveitis | Recruiting | Not stated | 2026-07-21 | NCT06974162 | |
| Adalimumab Dose Adjustment for Pediatric Uveitis Treatment Trial | anterior uveitis, eye disorder, intermediate uveitis, panuveitis, uveal disorder, uveitis | Not yet recruiting | Phase 4 | 2026-07-13 | NCT07699107 | |
| Multi-omics Study in Citrin Deficiency | Adult-onset citrullinemia type 2 | Active, not recruiting | Not stated | 2026-06-02 | NCT06895746 | |
| The Children's Adaptive Deep Brain Stimulation for Epilepsy Trial | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Epileptic Syndromes, Lennox-Gastaut syndrome, brain disorder, central nervous system disorder, epilepsy, hereditary disease, nervous system disorder | Recruiting | Not applicable | 2026-04-07 | NCT06924086 | |
| Gene Therapy With Modified Autologous Hematopoietic Stem Cells for Patients With Mucopolysaccharidosis Type II | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Neurobehavioral Manifestations, Neurologic Manifestations, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, X-linked disease, connective tissue disorder, cutaneous mucinosis, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, inherited neurodegenerative disorder, intellectual disability, lysosomal storage disease, metabolic disease, mucopolysaccharidosis, mucopolysaccharidosis type 2, nervous system disorder | Active, not recruiting | Phase 1 / Phase 2 | 2026-03-27 | NCT05665166 | |
| DTG/3TC Fixed Dose Formulations for the Maintenance of Virological Suppression in Children With HIV Infection Aged 2 to <15 Years Old | Blood-Borne Infections, Genital Diseases, HIV infectious disease, Infections, RNA Virus Infections, Urogenital Diseases, immune system disorder, inborn error of immunity, infectious disease, lentivirus infection, sexually transmitted disease, uterine carcinosarcoma, viral infectious disease, viral sexually transmitted disease | Active, not recruiting | Phase 2 / Phase 3 | 2026-03-04 | NCT04337450 | |
| Advanced MRI in IVH | Intraventricular Hemorrhage Neonatal; Post-hemorrhagic Hydrocephalus | Not yet recruiting | Not applicable | 2026-02-17 | NCT07412886 | |
| Thalamic Recordings in Children Undergoing SEEG | brain disorder, central nervous system disorder, epilepsy, focal epilepsy, nervous system disorder | Recruiting | Not applicable | 2026-02-02 | NCT06453759 | |
| Evaluation of Aid to Diagnosis for Congenital Dysplasia of the Hip in General Practice | Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hip Dislocation, Joint Dislocations, Musculoskeletal Abnormalities, arthropathy, developmental dysplasia of the hip, musculoskeletal system disorder | Active, not recruiting | Not applicable | 2026-01-15 | NCT04101903 | |
| Base Edited CAR T Cells Against AML: Deep Conditioning Ahead of Allogeneic Stem Cell Transplantation | Hemic and Lymphatic Diseases, Neoplasms by Histologic Type, acute myeloid leukemia, hematologic disorder, leukemia, myeloid leukemia, neoplasm | Active, not recruiting | Phase 1 | 2026-01-14 | NCT05942599 | |
| An Observational LTFU Study for Patients Previously Treated With Autologous ex Vivo Gene Therapy for ADA-SCID | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA repair disease, Infant, Newborn, Diseases, Nutritional and Metabolic Diseases, Primary Immunodeficiency Diseases, hereditary disease, immune system disorder, inborn error of immunity, metabolic disease, severe combined immunodeficiency, severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency | Enrolling by invitation | Not stated | 2025-12-18 | NCT04049084 | |
| Boost Brittle Bones Before Birth | Bone Diseases, Developmental, Collagen Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, bone disorder, connective tissue disorder, hereditary disease, musculoskeletal system disorder, osteochondrodysplasia, osteogenesis imperfecta | Active, not recruiting | Phase 1 / Phase 2 | 2025-09-12 | NCT03706482 | |
| Muscle Connective Tissue in Limb Development and Disease | Radial Dysplasia | Recruiting | Not stated | 2025-08-27 | NCT02611089 | |
| Repurposing Empagliflozin for DMD-associated Cardiomyopathy in Children 6-18 Years of Age | dilated cardiomyopathy 3B | Not yet recruiting | Phase 2 | 2025-08-15 | NCT06643442 | |
| Calprotectin and Gut Disease Study | Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, cardiovascular disorder, congenital heart disease, digestive system disorder, enterocolitis, gastroenteritis, heart disorder, intestinal disorder, necrotizing enterocolitis | Not yet recruiting | Not stated | 2025-08-08 | NCT07112794 | |
| CCHS Secure Health-hub Advancing Research Efforts (CCHS SHARE) | Disease Attributes, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease | Recruiting | Not stated | 2025-07-16 | NCT06554275 | |
| Primary Posterior Tracheopexy Prevents Tracheal Collapse | Cartilage Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Abnormalities, Digestive System Diseases, Musculoskeletal Abnormalities, Skin and Connective Tissue Diseases, Tracheobronchomalacia, congenital tracheomalacia, connective tissue disorder, digestive system disorder, esophageal atresia, esophageal atresia/tracheoesophageal fistula, esophageal disorder, musculoskeletal system disorder, respiratory system disorder, tracheal disorder | Enrolling by invitation | Not applicable | 2025-03-30 | NCT06335862 | |
| Gene Therapy with Modified Autologous Hematopoietic Stem Cells for Patients with Mucopolysaccharidosis Type IIIA | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mucopolysaccharidosis III, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, connective tissue disorder, cutaneous mucinosis, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, lysosomal storage disease, metabolic disease, mucopolysaccharidosis, mucopolysaccharidosis type 3A | Active, not recruiting | Phase 1 / Phase 2 | 2025-03-30 | NCT04201405 | |
| Gut Health in Children With Cancer | B-cell neoplasm, Burkitt lymphoma, DNA Virus Infections, Epstein-Barr virus infection, Hemic and Lymphatic Diseases, Herpesviridae infectious disease, Infections, Neoplasms by Histologic Type, Tumor Virus Infections, acute myeloid leukemia, hematologic disorder, hemophagocytic syndrome, immune system disorder, immunoproliferative disorder, leukemia, lymphatic system disorder, lymphoma, lymphoproliferative syndrome, myeloid leukemia, neoplasm, viral infectious disease | Recruiting | Not stated | 2025-03-28 | NCT06899581 | |
| Inherited Cardiac cONditions In Kids | cardiovascular disorder | Recruiting | Not stated | 2025-03-05 | NCT05158738 | |
| The Prevalence of RYR1-related Disease | Body Temperature Changes, Congenital Fiber Type Disproportion, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hyperthermia, Intraoperative Complications, Minicore Myopathy with External Ophthalmoplegia, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Postoperative Complications, Signs and Symptoms, Thomsen and Becker disease, central core myopathy, centronuclear myopathy, congenital myopathy, congenital structural myopathy, hereditary disease, inherited neurodegenerative disorder, malignant hyperthermia of anesthesia, muscle tissue disorder, musculoskeletal system disorder, myotonic syndrome, nemaline myopathy, nervous system disorder, neurodegenerative disease, neuromuscular disease | Not yet recruiting | Not stated | 2025-01-24 | NCT06791369 |