- Trials with a EudraCT protocol (44)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44 result(s) found for: Sleep paralysis.
Displaying page 1 of 3.
EudraCT Number: 2010-023756-82 | Sponsor Protocol Number: TUD-RaSPar-051 | Start Date*: 2011-07-13 | |||||||||||
Sponsor Name:Dresden University of Technology | |||||||||||||
Full Title: Rasagiline treatment for Sleep disorders in Parkinson´s disease | |||||||||||||
Medical condition: sleep disturbances/sleep disorders in patients with Parkinson´s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (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: 2011-000056-42 | Sponsor Protocol Number: SP0919 | Start Date*: 2011-10-07 | |||||||||||
Sponsor Name:UCB Celltech, UK - Registered Branch of UCB Pharma SA | |||||||||||||
Full Title: A MULTI-CENTRE, RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED STUDY TO EVALUATE THE EFFECTS OF ROTIGOTINE ON SLEEP EFFICIENCY IN PATIENTS WITH ADVANCED PARKINSON’S DISEASE | |||||||||||||
Medical condition: Advanced Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001176-15 | Sponsor Protocol Number: BIA-91067-405 | Start Date*: 2021-05-07 | |||||||||||
Sponsor Name:Bial - Portela & Ca, S.A. | |||||||||||||
Full Title: Open-label, single-arm, pilot study to evaluate the effect of opicapone 50 mg on Parkinson’s disease patients with end-of-dose motor fluctuations and associated sleep disorders. | |||||||||||||
Medical condition: Parkinson's disease patients with wearing-off motor fluctuations and associated sleep disorders. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001530-34 | Sponsor Protocol Number: PPVMvhH/146-2011/MvhH | Start Date*: 2012-08-09 | |||||||||||
Sponsor Name:VU University Medical Center [...] | |||||||||||||
Full Title: Varenicline, a partial nicotinic receptor agonist for the treatment of Excessive Daytime Sleepiness in Parkinson’s Disease: a placebo-controlled cross-over study | |||||||||||||
Medical condition: Idiopathic Parkinson's disease | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006907-35 | Sponsor Protocol Number: SP915 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Schwarz Biosciences GmbH | |||||||||||||
Full Title: Long-term extension of RECOVER A MULTICENTER, MULTINATIONAL, PHASE 3B, OPEN-LABEL EXTENSION TRIAL TO EVALUATE THE LONG-TERM EFFECT OF THE 24-HOUR TRANSDERMAL DELIVERY OF ROTIGOTINE ON MOTOR FUNCTI... | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) FI (Completed) ES (Completed) HU (Completed) IT (Completed) GB (Completed) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015833-66 | Sponsor Protocol Number: 50/0811 | Start Date*: 2009-01-20 | |||||||||||
Sponsor Name:CASA DI CURA PRIVATA S.RAFFAELE - PISANA | |||||||||||||
Full Title: Ropinirole 24h prolonged release and motor fluctuations: a study to control the wearing-off induced by dopamine agonists immediate release | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004238-85 | Sponsor Protocol Number: SPECT-IRBD | Start Date*: 2016-01-27 | |||||||||||
Sponsor Name:IDIBAPS | |||||||||||||
Full Title: Ictal brain SPECT in the premotor stage of Parkinson disease | |||||||||||||
Medical condition: Parkinson disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003966-25 | Sponsor Protocol Number: DEPOPA | Start Date*: 2008-12-23 | ||||||||||||||||
Sponsor Name:Universität Mainz, Klinik und Poliklinik für Neurologie | ||||||||||||||||||
Full Title: Double-blind, placebo controlled, randomised, monocenter cross-over studie to evaluate the effect of Desmopressin on the nocturnal polyuria in patients with idiopathic Parkinson Syndrome compared t... | ||||||||||||||||||
Medical condition: Effect of Desmopressin on the nocturnal polyuria in patients with idiopathic Parkinson Syndrome | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003512-57 | Sponsor Protocol Number: P 07-02/BF 2.649 | Start Date*: 2007-08-24 | ||||||||||||||||
Sponsor Name:Bioprojet | ||||||||||||||||||
Full Title: Randomized, dose-finding study of BF 2.649 5, 10, 20 and 40 mg/d in comparison to placebo in Excessive Daytime Sleepiness in Parkinson’s Disease patients (PD) | ||||||||||||||||||
Medical condition: Excessive daytime sleepiness associated to Parkinson disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-000877-35 | Sponsor Protocol Number: BB-2001-201b | Start Date*: 2017-08-09 | |||||||||||
Sponsor Name:BenevolentAI Bio | |||||||||||||
Full Title: Dose finding phase IIb study of Bavisant to evaluate its safety and efficacy in treatment of excessive daytime sleepiness (EDS) in parkinson’s Disease (PD). | |||||||||||||
Medical condition: Excessive daytime sleepiness with Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) ES (Completed) GB (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004865-26 | Sponsor Protocol Number: M12-927 | Start Date*: 2015-08-27 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: An Open-label, Randomized 26-Week Study Comparing Levodopa-Carbidopa INteStInal Gel (LCIG) Therapy to Optimized Medical Treatment (OMT) on Non-Motor Symptoms (NMS) in Subjects with Advanced Parkins... | |||||||||||||
Medical condition: Non-motor symptoms in advanced Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) SE (Completed) IT (Completed) ES (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020299-42 | Sponsor Protocol Number: KKS-135 | Start Date*: 2011-08-30 | |||||||||||
Sponsor Name:Philipps-University Marburg | |||||||||||||
Full Title: A randomized, placebo-controlled, double-blind, multi-center trial to assess the disease-modifying potential of transdermal nicotine in early Parkinson's disease in Germany and the USA (NIC-PD) | |||||||||||||
Medical condition: Early PD subjects within 18 months of diagnosis and not expected to require dopamine agonist or levodopa therapy for 1 year, with Hoehn and Yahr stage <2, with stable (>2 months) MAO-B inhibitor th... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001329-33 | Sponsor Protocol Number: S187.3.005 | Start Date*: 2009-10-02 | |||||||||||
Sponsor Name:AbbVie Inc | |||||||||||||
Full Title: Open-Label Continuation Treatment Study With Levodopa – Carbidopa Intestinal Gel In Subjects With Advanced Parkinson's Disease And Severe Motor-Fluctuations Who Have Exhibited A Persistent And Posi... | |||||||||||||
Medical condition: Treatment with Levodopa – Carbidopa Intestinal Gel in subjects with advanced Parkinson's disease and severe motor-fluctuations who have exhibited a persistent and positive effect to treatment in pr... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) CZ (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005011-52 | Sponsor Protocol Number: BIA-91067-303 | Start Date*: 2021-05-12 | |||||||||||
Sponsor Name:BIAL – Portela & Cª, S.A. | |||||||||||||
Full Title: A Phase III, Double-Blind, Randomized, Placebo-Controlled and Parallel Group Study to Evaluate the Efficacy and Safety of Opicapone, as Add on to Stable Levodopa (L-DOPA) Plus a Dopa Decarboxylase ... | |||||||||||||
Medical condition: Early Idiopathic Parkinson’s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) BG (Completed) PT (Completed) FR (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006752-35 | Sponsor Protocol Number: SP889 | Start Date*: 2007-05-09 | |||||||||||
Sponsor Name:Schwarz Biosciences GmbH | |||||||||||||
Full Title: RECOVER: RANDOMIZED EVALUATION OF THE 24-HOUR COVERAGE: EFFICACY OF ROTIGOTINE PHASE 3B, MULTICENTER, MULTINATIONAL, DOUBLE-BLIND, PLACEBO CONTROLLED, 2-ARM TRIAL TO EVALUATE THE EFFECT OF THE 24-H... | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) DE (Prematurely Ended) ES (Completed) HU (Completed) IT (Completed) AT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002609-66 | Sponsor Protocol Number: SP825 | Start Date*: 2004-12-06 |
Sponsor Name:Schwarz Biosciences GmbH | ||
Full Title: A phase 3, randomized, open-label, two-arm, parallel-group, multicenter, multinational trial to compare the efficacy of rotigotine transdermal patch to that of ropinirole on early morning motor imp... | ||
Medical condition: Parkinson's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000578-53 | Sponsor Protocol Number: S187.3.003 | Start Date*: 2009-05-08 | |||||||||||
Sponsor Name:Abbott Laboratories | |||||||||||||
Full Title: Open-Label, 12-Month Safety and Efficacy Study of Levodopa – Carbidopa Intestinal Gel in Levodopa-Responsive Parkinson's Disease Subjects | |||||||||||||
Medical condition: Treatment of levodopa-responsive Parkinson's subjects with severe motor fluctuations. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004565-13 | Sponsor Protocol Number: GR-2018-12366771 | Start Date*: 2022-09-08 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS ISTITUTO NEUROLOGICO CARLO BESTA | |||||||||||||
Full Title: Ambroxol as a disease-modifying treatment to reduce the risk of cognitive impairment in GBA-associated Parkinson's disease. A multicenter, randomized, double-blind, placebo-controlled, phase 2 trial. | |||||||||||||
Medical condition: Parkinson's disease associated to mutation on the GBA1 gene | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005186-18 | Sponsor Protocol Number: S187.3.004 | Start Date*: 2007-11-16 | |||||||||||
Sponsor Name:Solvay Pharmaceuticals B.V. | |||||||||||||
Full Title: Open-Label, 6-12 Months Safety and Efficacy Study of Levodopa – Carbidopa Intestinal Gel in Levodopa-Responsive Subjects with Advanced Parkinson's Disease and Severe Motor-Fluctuations | |||||||||||||
Medical condition: Treatment of levodopa-responsive Parkinson's subjects with severe motor fluctuations. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) PT (Completed) IT (Completed) CZ (Completed) ES (Completed) NL (Completed) GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
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