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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
ARTEMIS - The ARTEMIS Cohortcerebral palsy, ataxic, autosomal recessive, neurodevelopmental disorder, psychiatric disorderRecruitingNot stated2026-08-27NCT07421219
Test-retest Trial With [11C]MODAG-005 in PD or MSA and AMHC - Pilot PhaseNerve Degeneration, Parkinson disease, Pathologic Processes, Pathological Conditions, Signs and Symptoms, autonomic nervous system disorder, basal ganglia disorder, brain disorder, cardiovascular disorder, central nervous system disorder, hypotensive disorder, movement disorder, multiple system atrophy, nervous system disorder, neurodegenerative disease, parkinsonian disorder, primary dysautonomia, synucleinopathy, vascular disorderRecruitingEarly phase 12026-07-31NCT07640542
Oral N-acetylcysteine for Retinitis PigmentosaAbnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Deaf-Blind Disorders, Deafness, Ear Diseases, Eye Diseases, Hereditary, Hearing Loss, Sensorineural, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, Usher syndrome, blindness (disorder), eye disorder, hearing disorder, hearing loss disorder, hereditary disease, inherited retinal dystrophy, nervous system disorder, otorhinolaryngologic disease, retinal degeneration, retinal disorder, retinitis pigmentosa, vision disorderActive, not recruitingPhase 32026-06-15NCT05537220
WB-EMS Effects on Cardiometabolic Risk FactorsBody Weight, Dyslipidemias, Hypercholesterolemia, Insulin Resistance, Lipid Metabolism Disorders, Nutritional and Metabolic Diseases, Overweight, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, cardiovascular disorder, glucose metabolism disease, hyperinsulinism, hyperlipidemia, hypertensive disorder, hypertriglyceridemia, metabolic disease, nutritional disorder, obesity disorder, overnutrition, vascular disorderActive, not recruitingNot applicable2026-05-14NCT07406191
COMBINED PSMA-PET/CT AND MRI STAGING IN INTERMEDIATE AND HIGH-RISK PATIENTS PROSTATA-CANCER (COMBINE-P)Genital Diseases, Male Urogenital Diseases, Neoplasms by Site, Urogenital Diseases, Urogenital Neoplasms, male reproductive organ cancer, male reproductive system disorder, neoplasm, prostate cancer, prostate disorderActive, not recruitingNot stated2026-03-06NCT07455097
Effects of the Clinical Application of Traditional, Complementary and Integrative Medicine (TCIM) Procedures During Inpatient Stays in GermanyChronic Disease, Disease Attributes, Pathologic Processes, Pathological Conditions, Signs and SymptomsRecruitingNot stated2025-12-26NCT07040475
Study of BEST1 Vitelliform Macular DystrophyCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, eye disorder, hereditary disease, inherited retinal dystrophy, macular degeneration, retinal degeneration, retinal disorder, retinitis pigmentosa, vitelliform macular dystrophyRecruitingNot stated2025-07-30NCT05809635
Intersession Processes in Psychotherapeutic Treatments Using an Ecological Momentary Assessment Approach (ISA-Bell)depressive disorderRecruitingNot applicable2025-06-25NCT05553197
Interventions to Decrease CRE Colonization and Transmission Between Hospitals, Households, Communities and Domesticated AnimalsAntibiotic Resistant Infection; Carbapenem-Resistant Enterobacteriaceae InfectionRecruitingNot applicable2025-06-24NCT05871476
Natural History Study of Patients with HPDL MutationsBrain Diseases, Metabolic, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Leukoencephalopathies, Neurologic Manifestations, Nutritional and Metabolic Diseases, Paraplegia, Spastic, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, brain disorder, central nervous system disorder, central nervous system malformation, hereditary disease, hereditary motor and sensory neuropathy, hereditary spastic paraplegia, inborn mitochondrial metabolism disorder, inborn mitochondrial myopathy, inherited neurodegenerative disorder, metabolic disease, mitochondrial encephalomyopathy, muscle tissue disorder, musculoskeletal system disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, palsy, paraplegia, peripheral nervous system disorder, polyneuropathyRecruitingNot stated2025-03-30NCT05848271
Artificial Intelligence Based Melanoma Early Diagnosis and Risk Prediction in Children, Adolescents and Young AdultsNeoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, Skin and Connective Tissue Diseases, childhood malignant neoplasm, melanocytic neoplasm, melanoma, neoplasm, neuroendocrine neoplasm, primitive neuroectodermal tumor, skin disorder, skin neoplasmRecruitingNot stated2024-10-01NCT06621810
The Transplant Cohort of the German Center for Infection ResearchInfectionsRecruitingNot stated2024-04-23NCT06346665