- Trials with a EudraCT protocol (259)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
259 result(s) found for: Parkinsonism.
Displaying page 1 of 13.
EudraCT Number: 2012-000364-21 | Sponsor Protocol Number: PI1102031 | Start Date*: 2012-11-13 | |||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomédica | |||||||||||||
Full Title: FDDNP-PET FOR IN VIVO DIAGNOSIS OF TAUOPATHY IN UNCLASSIFIABLE PARKINSONISM | |||||||||||||
Medical condition: Atypical Parkinsonism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002216-25 | Sponsor Protocol Number: PDT409 | Start Date*: 2006-06-26 |
Sponsor Name:Amersham Health, S.A. (filial de GE Healthcare Ltd) | ||
Full Title: Ensayo en fase 4 multicéntrico, aleatorizado, abierto y comparativo para evaluar las modificaciones en el manejo clínico después de una tomografía con DaTSCAN en sujetos con parkinsonismo clínicame... | ||
Medical condition: The subjects included in this trial will have clinically uncertain parkinsonism in a general neurologist setting. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) IT (Completed) DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-000801-30 | Sponsor Protocol Number: E2007-G000-318 | Start Date*: 2007-08-01 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: A Multi-centre, Open Label Extension Study to Evaluate the Long-term Safety, Tolerability, and Efficacy of E2007 as an Adjunctive Therapy in Levodopa Treated Parkinson's Disease Subjects with Motor... | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) LV (Prematurely Ended) LT (Prematurely Ended) EE (Prematurely Ended) PL (Completed) FR (Completed) ES (Completed) IT (Completed) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002339-26 | Sponsor Protocol Number: E2007-G000-303 | Start Date*: 2006-10-05 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: A Multi-centre, Open Label Extension Study to Evaluate the Long-term Safety, Tolerability and Efficacy of E2007 as an Adjunctive Therapy in Levodopa Treated Parkinson's Disease Patients with Motor ... | |||||||||||||
Medical condition: Levodopa treated Parkinson's disease patients with motor fluctuations. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) EE (Completed) CZ (Completed) HU (Completed) BE (Completed) SE (Prematurely Ended) GB (Prematurely Ended) AT (Prematurely Ended) DE (Completed) ES (Completed) PT (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003045-26 | Sponsor Protocol Number: Pearl-PD | Start Date*: 2015-10-23 | |||||||||||
Sponsor Name:Umeå University Hospital | |||||||||||||
Full Title: [18F] FE-PE2I PET/CT study of Dopamine Transporters in Early Parkinsonian disease. | |||||||||||||
Medical condition: Patients with newly clinically diagnosed untreated idiopathic parkinsonism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004290-19 | Sponsor Protocol Number: SP873 | Start Date*: 2006-01-25 | |||||||||||
Sponsor Name:Schwarz Biosciences GmbH | |||||||||||||
Full Title: A double-blind, placebo-controlled, parallel group, proof of concept trial to assess the tolerabiltiy, safety and efficacy of rotigotine nasal spray for the acute treatment of 'off' symptoms in sub... | |||||||||||||
Medical condition: advanced-stage, idiopathic Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002467-27 | Sponsor Protocol Number: 2007 Neuro 12 | Start Date*: 2008-01-24 | |||||||||||||||||||||
Sponsor Name:Salford Royal NHS Foundation Trust | |||||||||||||||||||||||
Full Title: Antidyskinetic Properties of Topiramate: A Double-Blind, Placebo-Controlled Trial in Patients with Parkinson's Disease and Levodopa-Induced Dyskinesias | |||||||||||||||||||||||
Medical condition: Patients with idiopathic Parkinson's disease and levodopa-induced dyskinesias | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-017182-38 | Sponsor Protocol Number: IPX066-B09-03 | Start Date*: 2010-05-14 | |||||||||||
Sponsor Name:Impax Laboratories, Inc. acting through its Impax Pharmaceutical Division (Impax) | |||||||||||||
Full Title: An Open-Label Extension Study of the Safety and Clinical Utility of IPX066 in Subjects with Parkinson´s Disease | |||||||||||||
Medical condition: Idiopathic Parkinson´s disease (paralysis agitans) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) LV (Completed) LT (Completed) DE (Completed) PL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001416-42 | Sponsor Protocol Number: TVP-1012/500 | Start Date*: 2005-09-15 | |||||||||||
Sponsor Name:Teva Pharmaceuticals Industries LtD | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized Start, Placebo-Controlled, Parallel-Group Study to Assess Rasagiline as a Disease Modifying Therapy in Early Parkinson’s Disease Subjects | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) IT (Completed) ES (Completed) AT (Completed) PT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005234-39 | Sponsor Protocol Number: 2939111 | Start Date*: 2005-05-27 | |||||||||||
Sponsor Name:Orion Corporation, ORION PHARMA, Finland | |||||||||||||
Full Title: Multicentre, randomised, double-blind study to compare Stalevo® to levodopa/carbidopa in patients with Parkinson's disease experiencing symptoms of early wearing-off | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) DK (Completed) FI (Completed) IE (Completed) DE (Completed) LT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002697-37 | Sponsor Protocol Number: 14/0382 | Start Date*: 2015-04-15 | ||||||||||||||||
Sponsor Name:University College London | ||||||||||||||||||
Full Title: Single-centre open label exploratory phase IIb pilot study of exogenous oral Melatonin for the treatment of Nocturia in adults with Parkinson’s disease | ||||||||||||||||||
Medical condition: Parkinson's Disease Nocturia | ||||||||||||||||||
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Population Age: | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-011541-24 | Sponsor Protocol Number: TVP-1012/501 | Start Date*: 2009-10-09 | |||||||||||
Sponsor Name:Teva Pharmaceutical Industries Ltd | |||||||||||||
Full Title: An Open-Label, Multi-Center, Follow-Up Study Designed to Evaluate the Long-Term Effects of Rasagiline in Parkinson's Disease Subjects who Participated in the ADAGIO Study | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) NL (Completed) HU (Completed) FR (Completed) ES (Completed) IT (Completed) DE (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004795-19 | Sponsor Protocol Number: 120824001 | Start Date*: 2013-03-12 | |||||||||||
Sponsor Name:Folktandvården Västra Götaland | |||||||||||||
Full Title: Utilisation of botulinum toxin type A on masticatory muscel hyperactivity in CP - a randomized, controlled study. | |||||||||||||
Medical condition: Masticatory muscle hyperactivity/bruxism in patients with Cerebral Palsy. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000148-40 | Sponsor Protocol Number: PDSTAT2015 | Start Date*: 2015-11-09 | ||||||||||||||||
Sponsor Name:Plymouth Hospitals NHS Trust | ||||||||||||||||||
Full Title: Simvastatin as a neuroprotective treatment for Parkinson's disease: a double-blind, randomised, placebo controlled futility study in patients of moderate severity. | ||||||||||||||||||
Medical condition: Parkinson's disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-000833-12 | Sponsor Protocol Number: NW-1015/015/III/2003 | Start Date*: 2004-12-02 | |||||||||||
Sponsor Name:Newron Pharmaceuticals S.p.A. | |||||||||||||
Full Title: A phase III, double-blind, placebo-controlled study to determine the efficacy and safety of a low (50-100 mg/day) and high (150-200 mg/day) dose range of safinamide, as add-on therapy, in patients ... | |||||||||||||
Medical condition: Early idiopathic Parkinson’s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000835-27 | Sponsor Protocol Number: NW-1015/017/III/2003 | Start Date*: 2004-12-03 | |||||||||||
Sponsor Name:NEWRON PHARMACEUTICALS | |||||||||||||
Full Title: A phase III, double-blind, placebo-controlled, 12-month extension study to investigate the efficacy and safety of a dose range of safinamide of 50-200 mg/day, as add-on therapy in patients with ear... | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008210-38 | Sponsor Protocol Number: 2008_02/0841 | Start Date*: 2009-04-16 | ||||||||||||||||
Sponsor Name:Chru de Lille | ||||||||||||||||||
Full Title: Effet d’un traitement anti-glutamatergique sur les troubles de la marche avec freezing et sur l’attention dans la maladie de Parkinson: “freezing of gait and glutamate: FOGG-I” | ||||||||||||||||||
Medical condition: Patients ayant une maladie de Parkinson Patients à un stade évolué de la maladie avec des troubles de la marche sévères | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-010193-38 | Sponsor Protocol Number: IPX066-B08-05 | Start Date*: 2009-06-02 | |||||||||||
Sponsor Name:IMPAX Pharmaceuticals a Division of IMPAX Laboratories, Inc. | |||||||||||||
Full Title: A Placebo-Controlled Study to Evaluate the Safety and Efficacy of IPX066 in Subjects with Parkinson's Disease | |||||||||||||
Medical condition: Idiopathic Parkinson's disease (paralysis agitans) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) EE (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021394-37 | Sponsor Protocol Number: SP0976 | Start Date*: 2011-03-08 | |||||||||||
Sponsor Name:UCB Pharma SA | |||||||||||||
Full Title: MULTICENTER, DOUBLE-BLIND, PLACEBO CONTROLLED, PARALLEL-GROUP, PHASE IV STUDY TO ASSESS THE EFFECT OF ROTIGOTINE ON NON-MOTOR SYMPTOMS IN PATIENTS WITH IDIOPATHIC PARKINSON’S DISEASE | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) BE (Completed) CZ (Completed) SK (Completed) ES (Completed) AT (Completed) BG (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001722-25 | Sponsor Protocol Number: ZonMw80-83600-98-10226 | Start Date*: 2013-08-27 | |||||||||||
Sponsor Name:VU University Medical Center | |||||||||||||
Full Title: Cholinesterase inhibitors to slow progression of visual hallucinations in Parkinson’s disease: a multi-center placebo-controlled trial (CHEVAL) | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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