- Trials with a EudraCT protocol (91)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
91 result(s) found for: Sleep latency.
Displaying page 3 of 5.
EudraCT Number: 2016-000359-29 | Sponsor Protocol Number: CLFT218-1501 | Start Date*: 2016-11-09 | |||||||||||
Sponsor Name:Flamel Ireland Limited (trading under the business name Avadel Ireland) | |||||||||||||
Full Title: A Double-blind, Randomized, Placebo Controlled, Two Arm Multi-center Study to Assess the Efficacy and Safety of a Once Nightly Formulation of Sodium Oxybate for Extended-Release Oral Suspension (FT... | |||||||||||||
Medical condition: The treatment of cataplexy and excessive daytime sleepiness on narcolepsy. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DK (Prematurely Ended) DE (Completed) GB (Completed) FI (Completed) CZ (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001654-38 | Sponsor Protocol Number: TAK-861-2001 | Start Date*: 2023-05-26 | |||||||||||
Sponsor Name:Takeda Development Center Americas, Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of TAK-861 for the Treatment of Narcolepsy With Cataplexy (Narcolepsy Type 1) | |||||||||||||
Medical condition: Narcolepsy with cataplexy (Narcolepsy Type 1) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) NO (Completed) FI (Completed) SE (Completed) NL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018414-69 | Sponsor Protocol Number: 4305-029 | Start Date*: 2010-05-23 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: "Estudio de fase III, multicéntrico, aleatorizado, doble ciego, controlado con placebo, de grupos paralelos para evaluar la seguridad y la eficacia de MK-4305 en pacientes con insomnio primario -Es... | |||||||||||||
Medical condition: Insomnio Primario /Primary Insomnia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) GB (Completed) FI (Completed) SE (Completed) DK (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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: 2018-001166-42 | Sponsor Protocol Number: 152PO17433 | Start Date*: 2018-11-27 | |||||||||||
Sponsor Name:Aziende Chimiche Riunite Angelini Francesco ACRAF S.p.A (Angelini S.p.A.) | |||||||||||||
Full Title: A multi-centre, randomized, parallel-group, single blind Phase II trial to evaluate the pharmacokinetics and PKPD relationship of trazodone after single and repeated oral doses in children from 2 t... | |||||||||||||
Medical condition: Insomnia in children and adolescents with autism, intellectual disability or ADHD | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
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: 2017-004642-20 | Sponsor Protocol Number: ID-078A301 | Start Date*: 2018-07-02 | |||||||||||
Sponsor Name:Idorsia Pharmaceuticals Ltd | |||||||||||||
Full Title: Multi-center, double-blind, randomized, placebo-controlled, parallel-group, polysomnography study to assess the efficacy and safety of ACT-541468 in adult and elderly subjects with insomnia disorder | |||||||||||||
Medical condition: Insomnia disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) DE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004942-18 | Sponsor Protocol Number: LTE6673 | Start Date*: 2007-03-14 | |||||||||||
Sponsor Name:sanofi-aventis recherche et developpment | |||||||||||||
Full Title: Efficacy and safety of 2 mg/day of M100907 on Sleep Maintenance Insomnia with a sub-study of the effect of M100907 on stable Type II Diabetes Mellitus: a One Year, multi-center, randomized, double-... | |||||||||||||
Medical condition: sleep maintenance insomnia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) IT (Prematurely Ended) DE (Prematurely Ended) BE (Completed) ES (Completed) AT (Prematurely Ended) GR (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005194-56 | Sponsor Protocol Number: AC-057A301 | Start Date*: 2008-07-06 | |||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd | |||||||||||||
Full Title: Multi center, double blind, randomized, placebo controlled, active reference, parallel group polysomnography study to assess the efficacy and safety of a 16 day oral administration of ACT 078573 in... | |||||||||||||
Medical condition: Chronic primary insomnia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) SE (Completed) AT (Completed) HU (Completed) SK (Completed) DE (Completed) FI (Completed) ES (Completed) CZ (Completed) FR (Completed) DK (Completed) GB (Completed) IT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002965-13 | Sponsor Protocol Number: TAK-861-2003 | Start Date*: 2023-04-11 | |||||||||||
Sponsor Name:Takeda Development Center Americas, Inc. | |||||||||||||
Full Title: A Long-term Extension Study to Evaluate the Safety and Tolerability of TAK-861 in Participants With Selected Central Hypersomnia Conditions | |||||||||||||
Medical condition: Narcolepsy with Cataplexy (Type 1) and Narcolepsy without Cataplexy (Type 2) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Trial now transitioned) IT (Trial now transitioned) ES (Trial now transitioned) NL (Trial now transitioned) FR (Trial now transitioned) SE (Trial now transitioned) FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018413-30 | Sponsor Protocol Number: 4305-028 | Start Date*: 2010-05-25 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: "Estudio de fase III, multicéntrico, aleatorizado, doble ciego, controlado con placebo, de grupos paralelos para evaluar la seguridad y la eficacia de MK-4305 en pacientes con insomnio primario- Es... | |||||||||||||
Medical condition: Insomnio Primario / Priramy Insomnia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) FI (Completed) DK (Completed) SE (Completed) FR (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000980-33 | Sponsor Protocol Number: 42847922ISM2005 | Start Date*: 2018-06-11 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Parallel-Group, Active- and Placebo-Controlled Polysomnography Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42847922 in Subjects with Ins... | |||||||||||||
Medical condition: Insomnia Disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) PL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005510-20 | Sponsor Protocol Number: C10953/1100 | Start Date*: 2013-03-07 |
Sponsor Name:Cephalon, Inc. | ||
Full Title: A Randomized, Open-Label Study to Characterize the Pharmacokinetics, Pharmacodynamics, and Safety of Single and Multiple Doses of Armodafinil (50, 100, and 150 mg/day) in Children and Adolescents w... | ||
Medical condition: Excessive Sleepiness associated with Narcolepsy | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: FI (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-005514-31 | Sponsor Protocol Number: 14-003 | Start Date*: 2015-08-17 | |||||||||||
Sponsor Name:Jazz Pharmaceuticals Inc. | |||||||||||||
Full Title: A Twelve-Week, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group, Multicenter Study of the Safety and Efficacy of JZP 110 [(R)-2-amino-3-phenylpropylcarbamate hydrochloride] in the Treat... | |||||||||||||
Medical condition: Treatment of excessive sleepiness in adult patients with obstructive sleep apnea; to increase the ability to stay awake throughout the day. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005236-92 | Sponsor Protocol Number: 21106 | Start Date*: 2008-04-22 | |||||||||||
Sponsor Name:NV Organon | |||||||||||||
Full Title: A 6-month, double-blind, randomized, placebo-controlled, parallel group outpatient trial, investigating the efficacy and safety of Org 50081 in adult patients with chronic primary insomnia. | |||||||||||||
Medical condition: Primary insomnia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FR (Completed) HU (Prematurely Ended) SE (Completed) NL (Completed) DE (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006336-23 | Sponsor Protocol Number: AGO/2011/014 | Start Date*: 2013-07-01 | |||||||||||
Sponsor Name:University Hospital Ghent | |||||||||||||
Full Title: The effects of sodium oxybate in patients with chronic fatigue syndrome | |||||||||||||
Medical condition: Chronic fatigue syndrome | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
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: 2018-001311-79 | Sponsor Protocol Number: JZP080-301 | Start Date*: 2019-01-09 | ||||||||||||||||
Sponsor Name:Jazz Pharmaceuticals | ||||||||||||||||||
Full Title: A Double-blind, Placebo-controlled, Randomized Withdrawal, Multicenter Study of the Efficacy and Safety of JZP-258 in the Treatment of Idiopathic Hypersomnia (IH) with an Open-label Safety Extension | ||||||||||||||||||
Medical condition: Treatment of Idiopathic Hypersomnia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) GB (GB - no longer in EU/EEA) CZ (Completed) BE (Completed) DE (Completed) ES (Completed) FI (Completed) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-005487-15 | Sponsor Protocol Number: 14-002 | Start Date*: 2015-08-17 | |||||||||||
Sponsor Name:Jazz Pharmaceuticals Inc. | |||||||||||||
Full Title: A Twelve-week, Double-blind, Placebo-controlled, Randomized, Parallel-group, Multicenter Study of the Safety and Efficacy of JZP-110 [(R)-2-amino-3-phenylpropylcarbamate hydrochloride] in the Treat... | |||||||||||||
Medical condition: Treatment of excessive sleepiness in adult patients with narcolepsy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) NL (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004889-17 | Sponsor Protocol Number: MAD 105516 | Start Date*: 2006-05-23 |
Sponsor Name:GlaxoSmithKline Research and Development Limited | ||
Full Title: A randomized, double-blind, placebo-controlled, crossover study to evaluate the effects of morning administration of GW679769 (10mg and 30 mg) on polysomnograph sleep recordings, subjective sleep a... | ||
Medical condition: Primary insomnia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
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