- Trials with a EudraCT protocol (57)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
57 result(s) found for: Rivastigmine.
Displaying page 1 of 3.
EudraCT Number: 2014-003385-24 | Sponsor Protocol Number: 2815 | Start Date*: 2016-09-28 |
Sponsor Name:GGZ inGeest, parner VUmc | ||
Full Title: The Recall-study: Rivastigmine for ECT-induced Cognitive Adverse effects in Late Life Depression: a multicenter, randomized, double-blind, placebo-controlled, crossover trial | ||
Medical condition: Interictal delirium during electric convulsive therapy- course | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005633-33 | Sponsor Protocol Number: 202000842 | Start Date*: 2021-06-02 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Prediction of ECT treatment response and reduction of Cognitive Side-effects using EEG and Rivastigmine | ||
Medical condition: A depressive disorder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006166-42 | Sponsor Protocol Number: RIVA | Start Date*: 2007-07-17 |
Sponsor Name:University of Tuebingen | ||
Full Title: Exelon bei dementiellem Syndrom bei Patienten mit Progressiver Supranukleärer Parese - offene, prospektive Phase II-Studie - | ||
Medical condition: Progressive supranuclear palsy (PSP) is a neurodegenerative disorder with hardly any therapeutical option to ameliorate the course of the disease. Results of first trials with physostigmine and don... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000507-17 | Sponsor Protocol Number: SC1-04 | Start Date*: 2004-06-10 |
Sponsor Name:FONDAZIONE SANTA LUCIA | ||
Full Title: Effectiveness of rivastigmine treatment in post-stroke patients with right brain damage and unilateral spatial neglect | ||
Medical condition: Improvement of unilateral spatial neglect and functional status in right brain damaged patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003219-23 | Sponsor Protocol Number: 2844 | Start Date*: 2019-06-28 | ||||||||||||||||
Sponsor Name:University of Bristol | ||||||||||||||||||
Full Title: CHIEF-PD (CHolinesterase Inhibitor to prEvent Falls in Parkinson’s Disease): A phase 3 randomised double-blind placebo-controlled trial of rivastigmine to prevent falls in Parkinson’s disease | ||||||||||||||||||
Medical condition: This trial will investigate the effectiveness of Rivastigmine on prevention of falls in patients with Parkinson's disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003053-25 | Sponsor Protocol Number: 1466 | Start Date*: 2012-06-18 | |||||||||||
Sponsor Name:Research and Enterprise Department | |||||||||||||
Full Title: A randomised, double blind, placebo controlled trial to evaluate the effect of Rivastigmine on gait in people with Parkinson’s disease who have fallen. | |||||||||||||
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: 2006-004435-30 | Sponsor Protocol Number: SC06-02 | Start Date*: 2006-10-31 | |||||||||||
Sponsor Name:FONDAZIONE SANTA LUCIA | |||||||||||||
Full Title: Protocol of study for the evaluation of the efficacy of rivastigmine on cognitive and behavioural disorders, following traumatic brain injury TBI in chronic patients. | |||||||||||||
Medical condition: Patients with cognitive and behavioural disorders following severe TBI and other severe acquired brain injury Glasgow Coma Scale GCS lower or equal 8 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001383-46 | Sponsor Protocol Number: Sweet 0406 | Start Date*: 2004-10-25 |
Sponsor Name:Karolinska University Hospital, Huddinge | ||
Full Title: Swdeish Exelon Titration study | ||
Medical condition: Patients with possible or probable Alzheimer disease (AD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-008896-32 | Sponsor Protocol Number: MACS(Uni-Koeln-1260) | Start Date*: 2010-12-22 |
Sponsor Name:University of Cologne | ||
Full Title: Memory, Ageing, and the Cholinergic System a combined fMRI and PET study | ||
Medical condition: Patients with mild cognitive impairment (MCI) (50-80 years), who are at greater risk of developing alzheimer's dementia will be recruited in the present study and will be compared to an age-matched... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-000569-61 | Sponsor Protocol Number: CHUBX2016/27 | Start Date*: 2021-12-20 |
Sponsor Name:CHU de Bordeaux | ||
Full Title: Comparison of therapeutic strategies with Cholinesterase Inhibitors: stop or still (SOS) trial | ||
Medical condition: Alzheimer disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005300-41 | Sponsor Protocol Number: IC-DEL | Start Date*: 2008-05-27 | |||||||||||||||||||||||||||||||
Sponsor Name:University Medical Center Utrecht | |||||||||||||||||||||||||||||||||
Full Title: Rivastigmine for delirium in Intensive Care patients, a double-blind, randomised, placebo-controlled, multi-center add-on trial | |||||||||||||||||||||||||||||||||
Medical condition: Delirium | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003965-42 | Sponsor Protocol Number: 002 | Start Date*: 2007-12-04 | ||||||||||||||||
Sponsor Name:University Medical Centre Utrecht | ||||||||||||||||||
Full Title: Methylphenidate, rivastigmine or haloperidol in hypoactive delirious intensive care patients: a single centre, randomized, mono-blind pilot trial | ||||||||||||||||||
Medical condition: Hypoactive delirious ICU-patients | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000350-31 | Sponsor Protocol Number: CENA713B2315 | Start Date*: 2008-01-22 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A 76-week prospective, open-label, multicenter study to evaluate the long-term effect of Exelon® capsule and transdermal patch on worsening of the underlying motor symptoms of PD in patients with m... | |||||||||||||
Medical condition: Mild to moderately severe dementia associated with Parkinson’s disease (PDD). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007015-32 | Sponsor Protocol Number: CENA713DDE18 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A 16-week, multicenter, double-blind, randomized, placebo-controlled, parallel group study to evaluate the efficacy of rivastigmine (Exelon® patch 10 cm2) on cognitive deficits in patients with mul... | |||||||||||||
Medical condition: cognitive impairment in Multiple Sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005472-27 | Sponsor Protocol Number: 70639 | Start Date*: 2009-03-30 |
Sponsor Name:Medizinische Universität Innsbruck | ||
Full Title: Die antidementive Therapie mit Acetylcholinesteraseinhibitoren: Untersuchung von Plasmakonzentrationen, Arzneimittelinteraktionen und Therapieeffekt in Abhängigkeit von genetischen Polymorphismen | ||
Medical condition: Anhand der vorliegenden Studie soll untersucht werden, ob genetische Polymorphismen im CYP2D6-, im MDR1- oder im ACHE Gen mit sub- bzw. supratherapeutischen Wirkstoffspiegeln im Plasma, mit relevan... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (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) |
EudraCT Number: 2009-012071-10 | Sponsor Protocol Number: 268/09 | Start Date*: 2009-06-15 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: Rivastigmine in the treatment of Sleep REM Behaviour Disorder (RBD) and Hallucinations in Parkinsonism: a Clinical and Polysomnographic study | ||||||||||||||||||
Medical condition: PARKINSONISM | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001383-70 | Sponsor Protocol Number: CENA713DDE15 | Start Date*: 2007-09-26 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A 24 week, multicenter, open evaluation of the clinical effectiveness of the once-daily 10 cm2 Exelon® patch formulation in patients with probable Alzheimer’s disease (MMSE10-26) | |||||||||||||
Medical condition: probable Alzheimer's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015632-15 | Sponsor Protocol Number: P071244 | Start Date*: 2010-01-22 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Essai en double aveugle contre placebo d'un traitement par inhibiteur de l'acétyl cholinesterase sur l'évolution d'un syndrome confusionnel chez les plus de 75 ans et évolution vers un syndrome dém... | |||||||||||||
Medical condition: Syndrome confusionnel chez les personnes âgées de plus de 75 ans | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003405-27 | Sponsor Protocol Number: CENA 713D FR08 | Start Date*: 2007-09-10 | |||||||||||
Sponsor Name:NOVARTIS PHARMA SAS | |||||||||||||
Full Title: Etude ouverte, multicentrique, de 24 semaines, évaluant l'efficience clinique de la forme Exelon patch 10 cm2 chez des patients avec une maladie d'Alzheimer (MMSE 10-26) | |||||||||||||
Medical condition: Maladie d'Alzheimer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
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