- Trials with a EudraCT protocol (320)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (10)
320 result(s) found for: Sleep Disorder.
Displaying page 3 of 16.
EudraCT Number: 2006-005711-10 | Sponsor Protocol Number: OX22-006 | Start Date*: 2007-02-26 | |||||||||||
Sponsor Name:Orexo AB | |||||||||||||
Full Title: A double-blind, randomised, two-period crossover study to evaluate the hypnotic effects and safety of sublingual zolpidem for the treatment of insomnia. | |||||||||||||
Medical condition: Primary insomnia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001463-39 | Sponsor Protocol Number: E2006-G000-303 | Start Date*: 2017-04-04 | |||||||||||
Sponsor Name:Eisai Ltd. | |||||||||||||
Full Title: A Long-Term Multicenter, Randomized, Double-Blind, Controlled, Parallel-Group Study of the Safety and Efficacy of Lemborexant in Subjects With Insomnia Disorder | |||||||||||||
Medical condition: Treatment for insomnia disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) PL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003265-29 | Sponsor Protocol Number: 750598.01.003 | Start Date*: 2016-07-15 | |||||||||||
Sponsor Name:Dr. Willmar Schwabe GmbH & Co. KG | |||||||||||||
Full Title: Proof of concept trial to evaluate the effectiveness of combined treatment with Valerian extract (Euvegal®) and Lavender oil (Lasea®) in patients suffering from inability to fall or stay asleep | |||||||||||||
Medical condition: Nonorganic insomnia according to ICD 10 with the code F51.0 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001520-35 | Sponsor Protocol Number: MP-2019-001 | Start Date*: 2019-07-24 |
Sponsor Name:Hospital Gelderse Vallei | ||
Full Title: Efficacy of low dose amitriptyline vs. cognitive behavioural therapy for chronic insomnia and medical comorbidity: a randomized controlled non inferiority trial. | ||
Medical condition: Insomniadisorder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000826-21 | Sponsor Protocol Number: AC-078A201 | Start Date*: 2016-09-13 | |||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd | |||||||||||||
Full Title: Multi-center, double-blind, randomized, placebo-controlled, active reference, parallel-group, polysomnography dose response study to assess the efficacy and safety of ACT-541468 in adult subjects w... | |||||||||||||
Medical condition: Insomnia disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) HU (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003313-42 | Sponsor Protocol Number: AGO-TEA | Start Date*: 2012-03-29 |
Sponsor Name:Hospital General Universitario de Alicante | ||
Full Title: Efficacy of agomelatine on sleep disturbance in Autism Spectrum Disorder (ASD) | ||
Medical condition: The treatment of sleep disorders in patients with autism spectrum disorders (ASD) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004347-39 | Sponsor Protocol Number: E2006-G000-304 | Start Date*: 2016-10-21 |
Sponsor Name:Eisai Ltd. | ||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Active Comparator, Parallel-Group Study of the Efficacy and Safety of Lemborexant in Subjects 55 Years and Older with Insomnia Disorder | ||
Medical condition: Treatment for insomnia disorder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) ES (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-000030-39 | Sponsor Protocol Number: na | Start Date*: 2008-12-16 |
Sponsor Name:Ministery of Defense, Military Mental Health - Research Centre | ||
Full Title: Prazosin as add-on therapy in the pharmacological treatment of sleep disturbances in post traumatic stress disorder, a placebo-controlled study using polysomnography | ||
Medical condition: posttraumatic stress disorder (PTSD) | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004035-35 | Sponsor Protocol Number: NKI1103334 | Start Date*: 2007-12-19 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Devleopment Ltd | |||||||||||||
Full Title: A multi-centre, randomized, double-blind, placebo-controlled, cross-over study to evaluate the effects of GW597599 and GR205171 on sleep continuity, PSG sleep recordings, subjective sleep assessmen... | |||||||||||||
Medical condition: Primary insomnia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006677-25 | Sponsor Protocol Number: LTE6672 | Start Date*: 2007-07-10 |
Sponsor Name:sanofi-aventis recherche & développement | ||
Full Title: Efficacy and safety of 2mg/day of M100907 on Sleep Maintenance Insomnia with a sub-study of the effect of M100907 on stable Type II Diabetes Mellitus: a 12-week, multi-center, randomized, double-bl... | ||
Medical condition: Sleep maintenance insomnia (+ subpopulation of stable type II Diabetes Mellitus) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) CZ (Completed) FI (Completed) GR (Completed) IT (Completed) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003082-16 | Sponsor Protocol Number: LTE6262 | Start Date*: 2006-02-03 |
Sponsor Name:SANOFI-SYNTHELABO RECHERCHE | ||
Full Title: Efficacy and safety of eplivanserin 5mg/day on Sleep Maintenance Insomnia : a 12-week multicenter, randomized, double-blind, placebo-controlled study followed by an open treatment phase extension... | ||
Medical condition: SLEEP MAINTENANCE INSOMNIA | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) ES (Completed) CZ (Completed) AT (Completed) GB (Completed) NL (Completed) FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-004351-20 | Sponsor Protocol Number: TAK-375/EC302 | Start Date*: 2005-12-29 | |||||||||||
Sponsor Name:Takeda Global R&D Centre (Europe) | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled study to determine the long-term efficacy and safety of ramelteon in adults with chronic insomnia. | |||||||||||||
Medical condition: Chronic insomnia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) AT (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000319-21 | Sponsor Protocol Number: ClonDO | Start Date*: 2021-12-20 |
Sponsor Name:Charité – Universitätsmedizin Berlin | ||
Full Title: Treating Nightmares in Posttraumatic Stress Disorder with the α-adrenergic Agents Clonidine and Doxazosin: A Randomized-Controlled Feasibility Study (ClonDoTrial) | ||
Medical condition: Posttraumatic Stress Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004259-59 | Sponsor Protocol Number: AC-078A203 | Start Date*: 2017-01-31 | |||||||||||
Sponsor Name:Idorsia Pharmaceuticals Ltd | |||||||||||||
Full Title: Multi-center, single-arm, open-label study in patients with Insomnia Disorder to validate the Insomnia Daytime Symptoms and Impacts Questionnaire™ (IDSIQ™) | |||||||||||||
Medical condition: Insomnia disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020912-12 | Sponsor Protocol Number: VP-VEC-162-3202 | Start Date*: 2010-08-26 | |||||||||||
Sponsor Name:Vanda Pharmaceuticals Inc. | |||||||||||||
Full Title: Open-label safety study of a 1-year 20 mg dose regimen of tasimelteon for the treatment of Non-24-Hour Sleep-Wake Disorder (N24HSWD) in blind individuals with no light perception. | |||||||||||||
Medical condition: Non-24 Hour Sleep-Wake Disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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: 2006-004716-48 | Sponsor Protocol Number: CL3-20098-056 | Start Date*: 2007-02-14 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Effects of agomelatine (25 to 50 mg/day) on sleep EEG parameters compared to escitalopram in patients with Major Depressive Disorder. A 6-week randomised, double-blind parallel groups study versus ... | |||||||||||||
Medical condition: Major Depressive Disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) FR (Completed) AT (Completed) GB (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003154-40 | Sponsor Protocol Number: MK-4305-061 | Start Date*: 2017-01-11 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III Randomized, Placebo-Controlled Clinical Trial to Study the Safety and Efficacy of Suvorexant (MK-4305) for the Treatment of Insomnia in Subjects with Alzheimer’s Disease | |||||||||||||
Medical condition: Insomnia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003331-20 | Sponsor Protocol Number: D11443C00027 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Technical University Munich, Klinikum rechts der Isar | ||||||||||||||||||
Full Title: Effect of quetiapine XR on sleep in patients with major depression, as compared with mirtazapine | ||||||||||||||||||
Medical condition: During the past years, growing evidence of a pronounced antidepressant effect of quetiapine has been demonstrated in several studies; in the same time, quetiapine turned out to have sleep-promoting... | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-011014-17 | Sponsor Protocol Number: A0081165 | Start Date*: 2009-08-26 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017, US | |||||||||||||
Full Title: EFFECTS OF PREGABALIN ON SLEEP MAINTENANCE IN SUBJECTS WITH FIBROMYALGIA SYNDROME AND SLEEP MAINTENANCE DISTURBANCE: A RANDOMIZED PLACEBO-CONTROLLED 2-WAY CROSSOVER POLYSOMNOGRAPHY STUDY | |||||||||||||
Medical condition: SLEEP MAINTENANCE IN SUBJECTS WITH FIBROMYALGIA SYNDROME AND SLEEP MAINTENANCE DISTURBANCE | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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