| Sereda, Michael W |
HSP-PBP, NCT03981276: Phenotypes, Biomarkers and Pathophysiology in Hereditary Spastic Paraplegias and Related Disorders |
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| Recruiting | N/A | 2000 | Europe | Clinical rating scale to measure disease severity and progression, Spastic Paraplegia Rating Scale (SPRS), Next-Gen Sequencing (NGS) | Dr. Rebecca Schule, German Federal Ministry of Education and Research, German Center for Neurodegenerative Diseases (DZNE) | Hereditary Spastic Paraplegia | 08/39 | 08/41 | | |
| Hamm, Jacob |
| Recruiting | N/A | 639 | Europe | Proton pump inhibitor, LAMS-implantation | University Medical Center Goettingen, Technical University of Munich, Ludwig-Maximilians - University of Munich, University Hospital in Halle, University of Leipzig, University Hospital Heidelberg, Landesklinikum Sankt Polten, University Hospital Schleswig-Holstein, St. Josef Hospital Bochum, Klinikum Stadt Hanau, University Hospital, Aachen, University Hospital Regensburg | Acute Pancreatitis | 12/23 | 12/23 | | |
| Moser, Tobias |
NCT06680934: CABP2 Patient Registry and Natural History Study |
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| Recruiting | N/A | 100 | Europe | Molecular genetic testing and audiometry | University Medical Center Goettingen | CABP2-related Auditory Synaptopathy, Hearing Impairment | 08/49 | 08/49 | | |
NCT05946057: Otoferlin Patient Registry and Natural History Study |
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| Recruiting | N/A | 100 | Europe | Molecular genetic testing and audiometry | Tobias Moser | Otoferlin-related Auditory Synaptopathy, Hearing Impairment | 02/48 | 02/48 | | |
| Wollnik, Bernd |
NCT06680934: CABP2 Patient Registry and Natural History Study |
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| Recruiting | N/A | 100 | Europe | Molecular genetic testing and audiometry | University Medical Center Goettingen | CABP2-related Auditory Synaptopathy, Hearing Impairment | 08/49 | 08/49 | | |
NCT05946057: Otoferlin Patient Registry and Natural History Study |
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| Recruiting | N/A | 100 | Europe | Molecular genetic testing and audiometry | Tobias Moser | Otoferlin-related Auditory Synaptopathy, Hearing Impairment | 02/48 | 02/48 | | |
| Strenzke, Nicola |
NCT06680934: CABP2 Patient Registry and Natural History Study |
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| Recruiting | N/A | 100 | Europe | Molecular genetic testing and audiometry | University Medical Center Goettingen | CABP2-related Auditory Synaptopathy, Hearing Impairment | 08/49 | 08/49 | | |
NCT05946057: Otoferlin Patient Registry and Natural History Study |
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| Recruiting | N/A | 100 | Europe | Molecular genetic testing and audiometry | Tobias Moser | Otoferlin-related Auditory Synaptopathy, Hearing Impairment | 02/48 | 02/48 | | |
| Vona, Barbara |
NCT06680934: CABP2 Patient Registry and Natural History Study |
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| Recruiting | N/A | 100 | Europe | Molecular genetic testing and audiometry | University Medical Center Goettingen | CABP2-related Auditory Synaptopathy, Hearing Impairment | 08/49 | 08/49 | | |
NCT05946057: Otoferlin Patient Registry and Natural History Study |
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| Recruiting | N/A | 100 | Europe | Molecular genetic testing and audiometry | Tobias Moser | Otoferlin-related Auditory Synaptopathy, Hearing Impairment | 02/48 | 02/48 | | |
