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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Perioperative Systemic Therapies in Muscle-Invasive Bladder Cancer (GUARDIANS)Disease Attributes, Disease Progression, Neoplasms by Histologic Type, Pathologic Complete Response, Pathologic Processes, Pathological Conditions, Signs and Symptoms, carcinoma, epithelial neoplasm, neoplasm, transitional cell carcinomaRecruitingNot stated2026-10-02NCT07855926
Liver Transplantation for Non-Resectable Colorectal Liver Metastases Without Local Treatment OptionsDigestive System Diseases, Digestive System Neoplasms, Liver Neoplasms, Neoplasm Metastasis, Neoplasms by Site, Neoplastic Processes, Pathologic Processes, Pathological Conditions, Signs and Symptoms, colonic disorder, colorectal neoplasm, digestive system disorder, digestive system neoplasm, intestinal disorder, liver disorder, neoplasm, rectal disorderNot yet recruitingNot applicable2026-09-10NCT07811453
Goat Infant Formula Feeding and Eczema (the GIraFFE Study)Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eczema, Infantile, Hypersensitivity, Immediate, Skin Diseases, Eczematous, Skin and Connective Tissue Diseases, atopic eczema, dermatitis, hereditary disease, hereditary skin disorder, immune system disorder, skin disorderActive, not recruitingNot applicable2026-08-27NCT04599946
Intraoperative Confocal Laser Scanning Microscopy With Use of AI for Optimized Surgical Excision of Basal Cell CarcinomaNeoplasms by Histologic Type, basal cell carcinoma, basal cell neoplasm, carcinoma, epithelial neoplasm, neoplasmRecruitingNot stated2026-08-26NCT06600165
Study to Examine Lesions of the Skin Using Confocal Laser MicroscopyNeoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, Skin and Connective Tissue Diseases, basal cell carcinoma, basal cell neoplasm, benign neoplasm of skin, carcinoma, epithelial neoplasm, melanocytic neoplasm, melanoma, neoplasm, neuroendocrine neoplasm, primitive neuroectodermal tumor, skin disorder, skin neoplasm, squamous cell carcinoma, squamous cell neoplasmActive, not recruitingNot stated2026-08-26NCT06598137
Gustabor Phase 1 - AI-based Creation of a Nutritional Plan to Compensate for Chemotherapy-induced Taste DisordersBlood Protein Disorders, Digestive System Diseases, Digestive System Neoplasms, Hemic and Lymphatic Diseases, Neoplasms by Histologic Type, Neoplasms by Site, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, Taste Disorders, cardiovascular disorder, digestive system disorder, digestive system neoplasm, hematologic disorder, hemorrhagic disease, immune system disorder, immunoproliferative disorder, lymphoproliferative syndrome, monoclonal gammopathy, neoplasm, nervous system disorder, plasma cell neoplasm, vascular disorder, vascular hemostatic diseaseRecruitingNot applicable2026-08-21NCT07040189
Gustabor Phase 2 - Treating Taste Changes During Cancer Therapy: A Randomized Study Evaluating an AI- Based Nutrition InterventionBlood Protein Disorders, Digestive System Diseases, Digestive System Neoplasms, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Genitourinary Cancer, Hemic and Lymphatic Diseases, Male Urogenital Diseases, Neoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, Skin and Connective Tissue Diseases, Taste Disorders, Urogenital Diseases, Urogenital Neoplasms, cardiovascular disorder, digestive system disorder, digestive system neoplasm, hematologic disorder, hemorrhagic disease, immune system disorder, immunoproliferative disorder, lymphoproliferative syndrome, melanocytic neoplasm, melanoma, monoclonal gammopathy, neoplasm, nervous system disorder, neuroendocrine neoplasm, plasma cell neoplasm, primitive neuroectodermal tumor, skin disorder, skin neoplasm, vascular disorder, vascular hemostatic diseaseRecruitingNot applicable2026-08-20NCT07649681
Global Registry and Natural History Study for Mitochondrial DisordersAbnormalities, Multiple, Barth syndrome, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Cardiovascular Abnormalities, Cerebral Small Vessel Diseases, Chronic Disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Epilepsies, Myoclonic, Epilepsy, Generalized, Epileptic Syndromes, Kearns-Sayre syndrome, Leber hereditary optic neuropathy, Leigh syndrome, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, MELAS syndrome, MERRF syndrome, NARP syndrome, Neurologic Manifestations, Nutritional and Metabolic Diseases, Ocular Motility Disorders, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Pearson syndrome, Pyruvate Metabolism, Inborn Errors, Signs and Symptoms, X-linked disease, ataxia neuropathy spectrum, brain disorder, cardiomyopathy, cardiovascular disorder, central nervous system disorder, cerebrovascular disorder, coenzyme Q10 deficiency, congenital heart disease, cranial nerve neuropathy, epilepsy, eye disorder, heart disorder, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, inborn mitochondrial metabolism disorder, inborn mitochondrial myopathy, inherited retinal dystrophy, maternally-inherited diabetes and deafness, metabolic disease, mitochondrial encephalomyopathy, mitochondrial neurogastrointestinal encephalomyopathy, muscle tissue disorder, musculoskeletal system disorder, myelodysplastic syndrome, nervous system disorder, neuromuscular disease, ophthalmoplegia, palsy, progressive external ophthalmoplegia, progressive myoclonus epilepsy, retinal degeneration, retinal disorder, retinitis pigmentosa, spinocerebellar ataxia with epilepsy, vascular disorder, very long chain acyl-CoA dehydrogenase deficiencyRecruitingNot stated2026-08-07NCT05554835
TRICuspid Intervention in Heart Failure TrialHeart Failure Attributable to Severe Tricuspid RegurgitationActive, not recruitingNot applicable2026-05-22NCT04634266
TRICuspid Intervention and Invasive Hemodynamic Monitoring in Heart Failurecardiovascular disorder, heart disorder, heart failure, heart valve disorder, tricuspid valve insufficiencyRecruitingNot applicable2026-05-08NCT07442903
Widening Aims and Giving Patients a Voice for Expanded Structures in Breast Cancer Care Jointly Developed by Patients and PhysiciansNeoplasms by Site, Skin and Connective Tissue Diseases, breast cancer, breast disorder, breast neoplasm, neoplasm, skin disorderRecruitingNot stated2026-04-29NCT06416293
Fontan Outcomes in Oligemia vs Plethora in Univentricular CHDCardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hypovolemia, Pathologic Processes, Pathological Conditions, Signs and Symptoms, cardiovascular disorder, congenital heart disease, heart disorder, univentricular heartRecruitingNot stated2026-04-17NCT07535203
Assessment of Physical Activity and Cardiovascular Outcomes in Patients With Chronic Heart Failurecardiovascular disorder, heart disorder, heart failureRecruitingNot stated2026-03-11NCT07460531
Prospective Registry of Vertigo Due to Vertebrobasilar Transient Attacks.Disease Attributes, Dizziness, Ear Diseases, Emergencies, Neurologic Manifestations, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, Vertigo, brain disorder, brain ischemia, cardiovascular disorder, central nervous system disorder, cerebrovascular disorder, inner ear disorder, nervous system disorder, otorhinolaryngologic disease, transient ischemic attack, vascular disorder, vestibular disorderNot yet recruitingNot stated2026-02-27NCT07421973
Peripheral Neuropathy in Patients Receiving Enfortumab Vedotin and Pembrolizumab as First Line Treatment for Metastatic or Locally Advanced Urothelial CarcinomaNeoplasms by Histologic Type, carcinoma, epithelial neoplasm, neoplasm, nervous system disorder, neuromuscular disease, peripheral nervous system disorder, transitional cell carcinomaRecruitingNot stated2026-02-24NCT06657157
A Clincial Study Testing Tirzepatide on Reproductive Function and Metabolic Health in Women With PCOS Who Are Overweight or ObeseAdnexal Diseases, Body Weight, Cysts, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Genital Diseases, Nutritional and Metabolic Diseases, Overweight, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Urogenital Diseases, endocrine system disorder, female reproductive system disorder, gonadal disorder, neoplasm, nutritional disorder, obesity disorder, ovarian cyst, ovarian disorder, overnutrition, polycystic ovary syndromeRecruitingPhase 42026-01-08NCT07326111
Prospective Evaluation of Imaging Response Biomarkers During [177Lu]Lu-PSMA in Metastatic Castration-resistant Prostate CancerProstate Cancer Metastatic DiseaseRecruitingNot stated2025-12-26NCT06828263
Platform Assessing Regimens and Durations In a Global Multisite Consortium for TBActinomycetales infectious disease, Bacterial Infections and Mycoses, Infections, bacterial infectious disease, gram-positive bacterial infections, lung disorder, mycobacterial infectious disease, pulmonary tuberculosis, respiratory system disorder, respiratory tract infectious disorder, tuberculosisRecruitingPhase 22025-10-06NCT06114628
Early Life Malnutrition, Environmental Enteric Dysfunction and Microbiome TrajectoriesChild Malnutrition, Child Nutrition Disorders, Death, Digestive System Diseases, Infant Death, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, digestive system disorder, dysentery, gastroenteritis, intestinal disorder, nutritional deficiency disease, nutritional disorderRecruitingNot stated2025-09-26NCT07195006
Development and Validation of the FBIndex to Determine the Risk of Falls for Patients With Neuromuscular DisordersBrain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Chronic Disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Friedreich ataxia, Guillain-Barre syndrome, Lambert-Eaton myasthenic syndrome, Lysosomal Storage Diseases, Nervous System, Muscular Disorders, Atrophic, Neoplasms by Site, Nutritional and Metabolic Diseases, Paraneoplastic Syndromes, Nervous System, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Post-Infectious Disorders, Spinocerebellar Degenerations, TDP-43 proteinopathy, amyotrophic lateral sclerosis, autoimmune disease, autoimmune disorder of the nervous system, brain disorder, central nervous system disorder, central nervous system malformation, cerebellar disorder, chronic inflammatory demyelinating polyradiculoneuropathy, demyelinating disease, disorder of glycogen metabolism, facioscapulohumeral muscular dystrophy, glycogen storage disease II, hereditary disease, hereditary motor and sensory neuropathy, immune system disorder, inborn carbohydrate metabolic disorder, inborn errors of metabolism, inborn mitochondrial metabolism disorder, inclusion body myositis, inherited neurodegenerative disorder, lysosomal storage disease, metabolic disease, motor neuron disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myasthenia gravis, myositis disease, myotonic dystrophy, myotonic syndrome, neoplasm, nervous system disorder, neurodegenerative disease, neuromuscular disease, neuromuscular junction disease, paraneoplastic syndrome, peripheral nervous system disorder, polyneuropathy, polyradiculoneuropathy, proteostasis deficiencies, spinal cord disorder, spinal muscular atrophyEnrolling by invitationNot stated2025-09-10NCT06605612
Amino Acid PET-based Response Assessment in IDH-mutant Gliomas (APPEAR)Neoplasms by Histologic Type, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, astrocytoma (excluding glioblastoma), epithelial neoplasm, glioma, neoplasm, neuroepithelial neoplasm, oligodendroglioma, primitive neuroectodermal tumorRecruitingNot stated2025-09-08NCT07159607
Digital Assessment of Real-World Walking Activity in Pulmonary Hypertension: A Prospective Multicenter Trialcardiovascular disorder, hypertensive disorder, lung disorder, pulmonary arterial hypertension, pulmonary hypertension, respiratory system disorder, vascular disorderRecruitingNot stated2025-08-22NCT07137260
The Use of Assistive Gait Devices Can Reduce the Risk of Falls in Patients With Neuromuscular Diseases Following a Training Period.Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Chronic Disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Friedreich ataxia, Guillain-Barre syndrome, Lambert-Eaton myasthenic syndrome, Lysosomal Storage Diseases, Nervous System, Muscular Disorders, Atrophic, Myotonic Dystrophy 2, Neoplasms by Site, Nutritional and Metabolic Diseases, Paraneoplastic Syndromes, Nervous System, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Post-Infectious Disorders, Spinocerebellar Degenerations, autoimmune disease, autoimmune disorder of the nervous system, brain disorder, central nervous system disorder, central nervous system malformation, cerebellar disorder, chronic inflammatory demyelinating polyradiculoneuropathy, demyelinating disease, disorder of glycogen metabolism, facioscapulohumeral muscular dystrophy, glycogen storage disease II, hereditary disease, hereditary motor and sensory neuropathy, immune system disorder, inborn carbohydrate metabolic disorder, inborn errors of metabolism, inborn mitochondrial metabolism disorder, inclusion body myositis, inherited neurodegenerative disorder, limb-girdle muscular dystrophy, lysosomal storage disease, metabolic disease, motor neuron disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myasthenia gravis, myositis disease, myotonic dystrophy, myotonic syndrome, neoplasm, nervous system disorder, neurodegenerative disease, neuromuscular disease, neuromuscular junction disease, paraneoplastic syndrome, peripheral nervous system disorder, polyneuropathy, polyradiculoneuropathy, spinal cord disorder, spinal muscular atrophyEnrolling by invitationNot applicable2025-07-18NCT07072676
TIRCON International NBIA RegistryCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Familial apoceruloplasmin deficiency, Kufor-Rakeb syndrome, Woodhouse-Sakati syndrome, aceruloplasminemia, basal ganglia disorder, brain disorder, central nervous system disorder, fatty acid hydroxylase-associated neurodegeneration, hereditary disease, inherited neurodegenerative disorder, movement disorder, nervous system disorder, neuroaxonal dystrophy, neurodegeneration with brain iron accumulation, neurodegenerative disease, neuroferritinopathy, pantothenate kinase-associated neurodegenerationRecruitingNot stated2025-06-05NCT05522374
Improving the Outcomes of Children With Tuberculosis Through Innovative Diagnostics and Treatment MonitoringActinomycetales infectious disease, Bacterial Infections and Mycoses, Infections, bacterial infectious disease, gram-positive bacterial infections, mycobacterial infectious disease, tuberculosisRecruitingNot stated2025-02-07NCT06815588