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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Point of Care Fibrinogen Measurement in Trauma Patients in the Emergency DepartmentCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Deficiency, Fibrinogen, Hemic and Lymphatic Diseases, blood coagulation disease, coagulation protein disease, congenital afibrinogenemia, hematologic disorder, hemorrhagic disease, hereditary disease, inherited blood coagulation disorderRecruitingNot stated2026-10-06NCT07097337
Prevention of Opioid-induced Constipation in Patients With Advanced CancerCancer Pain, Chemically-Induced Disorders, Narcotic-Related Disorders, Neurologic Manifestations, Pain, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Signs and Symptoms, Digestive, constipation disorder, neoplasm, opioid-induced constipation, psychiatric disorder, substance-related disorderRecruitingPhase 42026-10-05NCT05216328
Efficacy of Antibiotic Treatment for Patients With Chronic Low Back Pain and Modic Type I Changes - Randomized Placebo-controlled TrialBack Pain, Low Back Pain, Neurologic Manifestations, Pain, Pathological Conditions, Signs and Symptoms, Signs and SymptomsActive, not recruitingPhase 32026-09-14NCT06771492
FCV vs VCV in Obstructive and Asthmatic Patientslung disorder, obstructive lung disease, respiratory system disorderRecruitingNot applicable2026-08-13NCT06563544
Secretin in Ex-situ Liver PerfusionLiver TransplantationEnrolling by invitationPhase 1 / Phase 22026-06-16NCT07651748
Prediction Models for LDLT OutcomesLiving Donor Liver TransplantationNot yet recruitingNot stated2026-02-03NCT07383194
Deep Phenotyping of CIndUChronic Disease, Disease Attributes, Hypersensitivity, Immediate, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, chronic inducible urticaria, chronic urticaria, familial dermatographia, immune system disorder, skin disorder, skin vascular disease, urticariaRecruitingNot stated2026-01-22NCT07359430
DEntal implaNt Set: Development and Implementation of a Standardized Outcome Set in Implant DentistryStomatognathic Diseases, Tooth Loss, mouth disorder, periodontal disorder, tooth disorderRecruitingNot stated2026-01-13NCT07337057
The Regenerative Capacity of the Donor Liver After Living Donor Liver Transplantation: an Ambidirectional Cohort StudyLiving Donor Liver TransplantationEnrolling by invitationNot stated2026-01-09NCT07329296
A Study on the Effects of Left Ventricular Unloading in the Setting of VA ECMO SupportInfarction, Necrosis, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Shock, Shock, Cardiogenic, cardiovascular disorder, heart disorder, ischemic disease, myocardial infarction, myocardial ischemia, vascular disorderRecruitingNot applicable2025-12-17NCT05913622
Steatosis Assessment Pre-LDLTLiving Donor Liver TransplantationEnrolling by invitationNot stated2025-12-11NCT07015723
DUPIlumab Dose REDUCtion in Patients With Controlled Atopic EczemaCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Hypersensitivity, Immediate, Skin Diseases, Eczematous, Skin and Connective Tissue Diseases, atopic eczema, dermatitis, hereditary disease, hereditary skin disorder, immune system disorder, skin disorderRecruitingPhase 42025-10-08NCT06004986
Prevention of PostAmputation Pain With Targeted Muscle ReinnervationNeoplasms by Histologic Type, Neoplasms, Nerve Tissue, Neurobehavioral Manifestations, Neurologic Manifestations, Pain, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Phantom Limb, Phantom Limb Pain, Postoperative Complications, Postoperative Pain, Signs and Symptoms, neoplasm, nerve sheath neoplasm, nervous system disorder, neuroma, perceptual disordersRecruitingNot applicable2025-09-19NCT06719245
A Study of Tividenofusp Alfa (DNL310) in Pediatric Participants With Hunter SyndromeCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Death, Death, Sudden, Infant Death, Neurobehavioral Manifestations, Neurologic Manifestations, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, Sudden Infant Death, 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 disorderActive, not recruitingPhase 1 / Phase 22025-08-07NCT04251026
The Correlation Between CT and MRCP Before Living Liver Donation for Liver Blood Vessel Assessment: an Ambidirectional Cohort StudyLiving Donor Liver TransplantationEnrolling by invitationNot stated2025-03-13NCT06875232
Unraveling the Blood Microbiome in Postoperative Recurrence of Crohn's DiseaseCrohn's Disease (CD)Not yet recruitingNot stated2025-01-13NCT06770140
Cryoablation of Brain NeoplasmBrain Metastases, Neoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, brain disorder, central nervous system cancer, central nervous system disorder, epithelial neoplasm, glioma, meningioma, neoplasm, nervous system disorder, neuroepithelial neoplasm, primitive neuroectodermal tumor, tumor of meninges, vascular cancerEnrolling by invitationNot applicable2024-12-31NCT06753617
Comparison of Standard Dose Alectinib to Alectinib in Adjusted Dose Based on Alectinib BloodlevelsNeoplasms by Site, Thoracic Neoplasms, bronchial neoplasm, bronchogenic carcinoma, lung cancer, lung disorder, lung neoplasm, neoplasm, non-small cell lung carcinoma, respiratory system disorder, respiratory tract neoplasmRecruitingPhase 42024-05-13NCT05525338
Cardiac Imaging in Adults With Congenital Aortic StenosisBicuspid Aortic Valve Disease, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, aortic valve disorder, cardiovascular disorder, congenital heart disease, heart disorder, heart valve disorderActive, not recruitingNot stated2024-03-12NCT05252351
The RECMAP-study: Resection With or Without Intraoperative Mapping for Recurrent GlioblastomaDisease Attributes, Neoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Recurrence, astrocytoma (excluding glioblastoma), brain disorder, brain glioblastoma, central nervous system cancer, central nervous system disorder, epithelial neoplasm, glioblastoma, glioma, neoplasm, nervous system disorder, neuroepithelial neoplasm, primitive neuroectodermal tumorRecruitingNot stated2024-02-22NCT06273176
The SUPRAMAX Study: Supramaximal Resection Versus Maximal Resection for High-Grade Glioma Patients (ENCRAM 2201)Brain Tumor, Primary, Neoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, anaplastic astrocytoma, astrocytoma (excluding glioblastoma), brain cancer, brain disorder, central nervous system cancer, central nervous system disorder, epithelial neoplasm, glioblastoma, glioma, malignant glioma, neoplasm, nervous system disorder, neuroepithelial neoplasm, primitive neuroectodermal tumorRecruitingNot stated2024-02-22NCT06118723
The PALSUR-study: Palliative Care Versus Surgery in High-grade Glioma Patients (ENCRAM 2203)Neoplasms by Histologic Type, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, astrocytoma (excluding glioblastoma), epithelial neoplasm, glioblastoma, glioma, neoplasm, neuroepithelial neoplasm, primitive neuroectodermal tumorRecruitingNot stated2023-11-27NCT06146738
The RESBIOP-study: Resection Versus Biopsy in High-grade Glioma Patients (ENCRAM 2202)Neoplasms by Histologic Type, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, astrocytoma (excluding glioblastoma), brain glioblastoma, epithelial neoplasm, glioblastoma, glioma, neoplasm, neuroepithelial neoplasm, primitive neuroectodermal tumorRecruitingNot stated2023-11-27NCT06146725
Growing up With the Young Endocrine Support System (YESS!)46 XY differences of sex development, Bone Diseases, Developmental, Bone Diseases, Endocrine, Cardiovascular Abnormalities, Combined Pituitary Hormone Deficiency, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dwarfism, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Klinefelter syndrome, Male Urogenital Diseases, Nutritional and Metabolic Diseases, Sex Chromosome Disorders, Thyroid Dysgenesis, Turner syndrome, Urogenital Abnormalities, Urogenital Diseases, X-linked disease, adrenal gland disorder, adrenocortical insufficiency, adrenogenital syndrome, androgen insensitivity syndrome, autoimmune disease, bone disorder, brain disorder, cardiovascular disorder, central nervous system disorder, chromosomal disorder, congenital adrenal hyperplasia, congenital heart disease, disorder of sexual differentiation, endocrine system disorder, gonadal disorder, gonadal dysgenesis, heart disorder, hereditary disease, hypogonadism, hypogonadotropic hypogonadism, hypopituitarism, hypothalamic disorder, immune system disorder, inborn errors of metabolism, metabolic disease, musculoskeletal system disorder, nervous system disorder, pituitary dwarfism, pituitary gland disorder, sex chromosome disorder of sex development, steroid inherited metabolic disorder, thyroid gland disorderNot yet recruitingNot applicable2023-09-07NCT04252001
GROWing Up With Rare GENEtic Syndromes22q11.2 deletion syndrome, 46 XY differences of sex development, 48,XXYY syndrome, Abnormalities, Multiple, Allan-Herndon-Dudley syndrome, Aortic Stenosis, Supravalvular, Bardet-Biedl syndrome, Blepharophimosis syndrome Ohdo type, Bone Diseases, Developmental, CHARGE syndrome, Cardiovascular Abnormalities, Ciliopathies, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Cytopenia, De Lange Syndrome, Deaf-Blind Disorders, Deafness, DiGeorge syndrome, Ear Diseases, Eye Diseases, Hereditary, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Imprinting Disorders, Jacobsen Distal 11q Deletion Syndrome, Kallmann syndrome, Klinefelter syndrome, Limb Deformities, Congenital, Lymphatic Abnormalities, Male Urogenital Diseases, Malformations of Cortical Development, Group I, Musculoskeletal Abnormalities, Neoplasms by Histologic Type, Neoplasms, Multiple Primary, Neoplasms, Nerve Tissue, Neurobehavioral Manifestations, Neurologic Manifestations, Noonan syndrome, Nutritional and Metabolic Diseases, Overweight, Pathological Conditions, Signs and Symptoms, Prader-Willi syndrome, Rett syndrome, Saethre-Chotzen syndrome, Sensation Disorders, Sex Chromosome Disorders, Signs and Symptoms, Skin and Connective Tissue Diseases, Turner syndrome, Urogenital Abnormalities, Urogenital Diseases, Williams syndrome, X-linked disease, adrenal gland disorder, adrenogenital syndrome, aortic valve disorder, aortic valve stenosis, blepharophimosis - intellectual disability syndrome, Ohdo type, blindness (disorder), blood platelet disease, bone disorder, brain disorder, cardiovascular disorder, central nervous system disorder, central nervous system malformation, cerebral cortical dysplasia, chromosomal disorder, coloboma, congenital adrenal hyperplasia, congenital heart disease, connective tissue disorder, craniosynostosis, disorder of sexual differentiation, dysostosis, endocrine system disorder, eye disorder, gonadal disorder, gonadal dysgenesis, hamartoma, hearing disorder, hearing loss disorder, heart disorder, heart valve disorder, hematologic disorder, hereditary disease, hereditary neoplastic syndrome, hypogonadism, hypoparathyroidism, hypothalamic disorder, inborn errors of metabolism, inherited neurodegenerative disorder, intellectual disability, lymphatic system disorder, metabolic disease, musculoskeletal system disorder, neoplasm, nerve sheath neoplasm, nervous system disorder, neurocutaneous syndrome, neurodegenerative disease, neurofibroma, neurofibromatosis, non-acquired combined pituitary hormone deficiency, nutritional disorder, obesity disorder, otorhinolaryngologic disease, overnutrition, parathyroid gland disorder, retinitis pigmentosa, sex chromosome disorder of sex development, steroid inherited metabolic disorder, syndactyly, synostosis, tetrasomy X, thrombocytopenia, tuberous sclerosis, velocardiofacial syndrome, vision disorderRecruitingNot stated2023-09-06NCT04463316