| Schöls, Ludger |
| Recruiting | N/A | 100 | Europe | | University Hospital Tuebingen | Movement Disorder, Cognitive Decline | 06/22 | 09/23 | | |
PROFA, NCT05943002: Patient-reported, Health Economic and Psychosocial Outcomes in Friedreich Ataxia |
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| Recruiting | N/A | 200 | Europe | | German Center for Neurodegenerative Diseases (DZNE), McMaster University, Sorbonne University | Friedreich Ataxia | 08/24 | 10/24 | | |
EFACTS, NCT02069509: Patient Registry of the European Friedreich's Ataxia Consortium for Translational Studies |
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| Recruiting | N/A | 1200 | Europe, RoW | | European Friedreich's Ataxia Consortium for Translational Studies | Friedreich's Ataxia | 12/24 | 12/24 | | |
NCT06623890: A Study to Learn More About the Long-Term Safety of BIIB141 (Omaveloxolone) in Participants With Friedreich's Ataxia Who Are Prescribed it for the First Time |
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| Recruiting | N/A | 300 | Europe, US, RoW | Omaveloxolone, SKYCLARYS, BIIB141 | Reata, a wholly owned subsidiary of Biogen | Friedreich Ataxia | 10/29 | 10/29 | | |
| Not yet recruiting | N/A | 5000 | NA | Data set as defined by the ERN Research Workgroup of the European Commission | University Hospital Tuebingen | Rare Diseases | 11/25 | 12/25 | | |
NCT03206190: The preSPG4 Study - Studying the Prodromal and Early Phase of SPG4 |
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| Recruiting | N/A | 200 | Europe | SPRS Score and clinical signs, Cognition Testing using CANTAB, Lumbar Puncture and blood draw, MRI, Electrophysiology, Testing functional performance, Non motor symptoms | University Hospital Tuebingen | Hereditary Spastic Paraplegia, Hereditary, Spastic Paraplegia, Autosomal Dominant | 12/29 | 12/31 | | |
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 | | |
| Recruiting | N/A | 3000 | Europe, Canada, US, RoW | | Friedreich's Ataxia Research Alliance | Friedreich Ataxia | 01/48 | 01/48 | | |
NCT05554835: Global Registry and Natural History Study for Mitochondrial Disorders |
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| Recruiting | N/A | 6000 | Europe | | LMU Klinikum, European Commission, German Federal Ministry of Education and Research, University of Pisa | Mitochondrial Diseases, Kearns-Sayre Syndrome, MIDD, SANDO, SCAE, NARP Syndrome, MELAS Syndrome, MERRF Syndrome, Coenzyme Q10 Deficiency, LHON, MNGIE, MIRAS, Barth Syndrome, MDS, Mitochondrial Myopathies, Leigh Syndrome, Pearson Syndrome, CPEO | 12/40 | 12/40 | | |
| Rattay, Tim W |
| Recruiting | N/A | 1236 | Europe, RoW | pre-pectoral breast reconstruction | IRCCS San Raffaele, EUBREAST ETS | Breast Cancer | 09/27 | 09/27 | | |
NCT03206190: The preSPG4 Study - Studying the Prodromal and Early Phase of SPG4 |
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| Recruiting | N/A | 200 | Europe | SPRS Score and clinical signs, Cognition Testing using CANTAB, Lumbar Puncture and blood draw, MRI, Electrophysiology, Testing functional performance, Non motor symptoms | University Hospital Tuebingen | Hereditary Spastic Paraplegia, Hereditary, Spastic Paraplegia, Autosomal Dominant | 12/29 | 12/31 | | |
