University of Tübingen and German Center for Neurodegenerative Diseases (DZNE) Tübingen
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 7 Trials 
14 Trials

   

Trial + Data / EventsStatusPhNRegionInterventionsSponsorConditionsPrimary complStudy compl
Schöls, Ludger
NextGen-SE, NCT02588638: Next Generation Sequencing Diagnostics - On the Road to Rapid Diagnostics for Rare Diseases

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

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

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

Recruiting
N/A
300
Europe, US, RoW
Omaveloxolone, SKYCLARYS, BIIB141
Reata, a wholly owned subsidiary of Biogen
Friedreich Ataxia
10/29
10/29
ERN-RND reg, NCT04319796: European Registry on Rare Neurological Diseases

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

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

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
UNIFAI, NCT06016946: Friedreich Ataxia Global Clinical Consortium UNIFIED Natural History Study

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

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
Schüle, Rebecca
SPAX-PBP, NCT04297891: Phenotypes, Biomarkers and Pathophysiology in Spastic Ataxias

Recruiting
N/A
250
Europe, Canada, RoW
Clinical rating scale to measure Ataxia disease severity and progression, Scale for the Assessment and rating of Ataxia (SARA), Clinical rating scale to measure spastic paraplegia disease severity and progression, Spastic Paraplegia Rating Scale (SPRS), Disease-specific severity index for adults with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), DSI-ARSACS, Next-Gen Sequencing (NGS)
Dr. Rebecca Schule, German Center for Neurodegenerative Diseases (DZNE), German Research Foundation
Spastic Ataxia
06/24
06/25
HSP-PBP, NCT03981276: Phenotypes, Biomarkers and Pathophysiology in Hereditary Spastic Paraplegias and Related Disorders

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
Dillmann, Katrin
HSP-PBP, NCT03981276: Phenotypes, Biomarkers and Pathophysiology in Hereditary Spastic Paraplegias and Related Disorders

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
Krägeloh-Mann, Ingeborg
HSP-PBP, NCT03981276: Phenotypes, Biomarkers and Pathophysiology in Hereditary Spastic Paraplegias and Related Disorders

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
Döbler-Neumann, Marion
HSP-PBP, NCT03981276: Phenotypes, Biomarkers and Pathophysiology in Hereditary Spastic Paraplegias and Related Disorders

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

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