- Trials with a EudraCT protocol (1,052)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,052 result(s) found for: Sleep study.
Displaying page 2 of 53.
EudraCT Number: 2023-000062-34 | Sponsor Protocol Number: Reb-Oxy-OSA | Start Date*: 2023-06-02 | |||||||||||
Sponsor Name:CHU Brugmann | |||||||||||||
Full Title: Combination of Reboxetine 4mg and Oxybutynin 5mg for treating moderate obstructive sleep apnea: a one-month randomized placebo-controlled double-blind study | |||||||||||||
Medical condition: Obstructive sleep apnea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003037-41 | Sponsor Protocol Number: MUG-EROS-2012 | Start Date*: 2012-09-21 | |||||||||||||||||||||
Sponsor Name:Medizinische Universität Graz, Universitätsklinik für Innere Medizin, Klinische Abteilung für Lungenkrankheiten | |||||||||||||||||||||||
Full Title: Effects of Roflumilast on pulmonary vascular resistance in patients with COPD and sleep apnea (Overlap Syndrome) with and without non-invasive ventilation. A Pilot Study. | |||||||||||||||||||||||
Medical condition: This study is about pulmonary hypertension due to lung diseases. The lung disease in this study will be the overlap syndrome which is defined as chronic obstructive pulmonary disease concomitant wi... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004520-35 | Sponsor Protocol Number: VP-VEC-162-3204 | Start Date*: 2012-12-06 | |||||||||||
Sponsor Name:Vanda Pharmaceuticals Inc. | |||||||||||||
Full Title: AN EXTENSION OPEN-LABEL SAFETY STUDY OF A 24-MONTH 20MG DOSE REGIMEN OF TASIMELTEON FOR THE TREATMENT OF NON-24-HOUR SLEEP-WAKE DISORDER (N24HSWD) IN BLIND INDIVIDUALS WITH NO LIGHT PERCEPTION WHO ... | |||||||||||||
Medical condition: Blind males or females with no conscious light perception and the complaint of a sleep-wake disorder associated with Non-24 Hour Sleep- Wake Disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015859-24 | Sponsor Protocol Number: Zon-001 | Start Date*: 2010-02-24 | |||||||||||
Sponsor Name:The Sahlgrenska Academy, University of Gothenburg | |||||||||||||
Full Title: | |||||||||||||
Medical condition: The objective is to explore the efficacy of pharmacological weight reduction compared with CPAP treatment in patients with moderate to severe obstructive sleep apnea (OSA). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004866-33 | Sponsor Protocol Number: CA-BP13 | Start Date*: 2014-04-04 | |||||||||||
Sponsor Name:Göteborgs Universitet | |||||||||||||
Full Title: A short term open, randomized cross over trial trial exploring the effect of carbonic anhydrase inhibition by acetazolamide on sleep apnea associated hypertension | |||||||||||||
Medical condition: obstructive sleep apnea related hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003939-32 | Sponsor Protocol Number: APL-510-008 | Start Date*: 2005-03-23 |
Sponsor Name:Alliance Pharmaceuticals Ltd | ||
Full Title: A double-blind placebo controlled cross-over study to determine if 1.5 and 3mg of APL510 can normalise sleep patterns in elderly subjects with difficulty in maintenance of sleep and/or initiating s... | ||
Medical condition: Difficulty in maintenance of sleep and/or initiating sleep onset | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003822-28 | Sponsor Protocol Number: EFC10480 | Start Date*: 2008-03-05 |
Sponsor Name:sanofi-aventis recherche et développement | ||
Full Title: Comparison of the safety and efficacy of eplivanserin and lormetazepam in the treatment of insomnia characterized by sleep maintenance difficulties. A 4 week, randomized, double-blind, comparative,... | ||
Medical condition: Chronic primary insomnia and sleep maintenance difficulties. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) PT (Completed) FR (Completed) ES (Completed) EE (Completed) FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005792-16 | Sponsor Protocol Number: Rocuronium_HVR_OSAS | Start Date*: 2012-02-10 | |||||||||||
Sponsor Name:Karolinska University Hospital | |||||||||||||
Full Title: Effect of reduced cholinergic transmission by rocuronium on the hypoxic ventilatory response in patients with obstructive sleep apnea - before and after three months of continous positive airway pr... | |||||||||||||
Medical condition: Obstuctive sleep apnea and acute hypoxic ventilatory response | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000220-18 | Sponsor Protocol Number: C.2524.0472.01 | Start Date*: 2013-03-25 |
Sponsor Name:University of Amsterdam | ||
Full Title: Effects of melatonin treatment, light therapy, and sleep improvement on psychosocial, cognitive, and behavioural outcomes in children with Delayed Sleep Phase Syndrome and their parents | ||
Medical condition: Delayed Sleep Phase Syndrome | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000281-35 | Sponsor Protocol Number: VP-VEC-162-3201 | Start Date*: 2011-06-09 | |||||||||||
Sponsor Name:Vanda Pharmaceuticals Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Mask, Placebo-Controlled, Parallel Study to Investigate the Efficacy and Safety of 20 mg Tasimelteon versus Placebo in Totally Blind Subjects with N24HSWD followed... | |||||||||||||
Medical condition: Blind males or females with no conscious light perception and the complaint of a sleep-wake disorder associated with Non-24 Hour Sleep-Wake Disorder. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003791-22 | Sponsor Protocol Number: EFC10844 | Start Date*: 2009-01-19 | |||||||||||
Sponsor Name:sanofi-aventis Recherche & Développement | |||||||||||||
Full Title: Efficacy and safety of eplivanserin 5mg/day in insomnia characterized by sleep maintenance difficulties: a 6-week, randomized, double-blind, placebo-controlled, polysomnography study | |||||||||||||
Medical condition: insomnia characterized by sleep maintenance difficulties | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) HU (Completed) DE (Completed) AT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000645-23 | Sponsor Protocol Number: Borealis1 | Start Date*: 2015-06-19 | ||||||||||||||||
Sponsor Name:CIBER (Centro de Investigacion Biomedica en Red) | ||||||||||||||||||
Full Title: Safety, tolerability and efficacy of nocturnal hypertension treatment with domperidone in the sleep apnea-hypopnea syndrome. Pilot study. | ||||||||||||||||||
Medical condition: Nocturnal hypertension in the sleep apnea-hypopnea syndrome. | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004620-10 | Sponsor Protocol Number: 719-13 | Start Date*: 2014-12-22 |
Sponsor Name:Johan Hellgren | ||
Full Title: A double blind, placebo controlled randomized study of nasal steroid spray treatment on the quality of life and objective sleep parameters in children with sleep disorder breathing. | ||
Medical condition: Sleep disordered breathing due to enlarged tonsils and/or adenoid | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-003460-31 | Sponsor Protocol Number: COP13.058 | Start Date*: 2014-03-03 |
Sponsor Name:GGZ-Drenthe | ||
Full Title: The effect of low doses of mirtazapine and quetiapine on sleep and daytime functioning. | ||
Medical condition: Insomnia | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003394-15 | Sponsor Protocol Number: VP-VEC-162-4201 | Start Date*: 2016-06-28 | |||||||||||
Sponsor Name:Vanda Pharmaceuitcals Inc. | |||||||||||||
Full Title: OPEN-LABEL STUDY TO INVESTIGATE THE PHARMACOKINETICS AND SAFETY OF TASIMELTEON IN TOTALLY BLIND CHILDREN AND ADOLESCENTS WITH NON-24-HOUR SLEEP- WAKE DISORDER | |||||||||||||
Medical condition: This study will be an open-label, single dose, non-controlled trial to evaluate the pharmacokinetics and safety of tasimelteon in children who are 3 years to less than 18 years of age, totally blin... | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004552-41 | Sponsor Protocol Number: I8F-MC-GPI2 | Start Date*: 2022-09-14 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Master Protocol to Investigate the Efficacy and Safety of Tirzepatide Once Weekly in Participants who have Obstructive Sleep Apnea and Obesity: A Randomized, Double-Blind, Placebo-Controlled Tria... | |||||||||||||
Medical condition: Obstructive sleep apnea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000520-19 | Sponsor Protocol Number: BAY2586116/20849 | Start Date*: 2021-02-10 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: Proof-of-concept, multi-center, randomized, double-blind, placebo-controlled, two-way crossover study to investigate the effect strength of BAY 2586116 on the apnea-hypopnea-index after repetitive ... | |||||||||||||
Medical condition: Sleep Apnea, Obstructive | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003766-27 | Sponsor Protocol Number: 848015011 | Start Date*: 2018-07-18 | |||||||||||
Sponsor Name:VU University Medical Centre | |||||||||||||
Full Title: The DREAMING study: Efficacy of low dose amitriptyline and mirtazapine for insomnia disorder: a double-blind, randomized, placebo-controlled trial in general practice | |||||||||||||
Medical condition: Insonnia disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001492-30 | Sponsor Protocol Number: EFC10550 | Start Date*: 2008-08-25 | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: Comparison of the safety and efficacy of volinanserin and lormetazepam in the treatment of insomnia characterized by sleep maintenance difficulties. A 4 week, randomized, double-blind, double-dummy... | |||||||||||||
Medical condition: Insomnia characterized by sleep maintenance difficulties | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) ES (Completed) FR (Completed) SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002116-32 | Sponsor Protocol Number: MTM-04 | Start Date*: 2015-09-23 | ||||||||||||||||||||||||||
Sponsor Name:Køge Hospital | ||||||||||||||||||||||||||||
Full Title: The effect of MElatonin on Depression, Anxiety, CIrcadian and Sleep disturbances in patients after acute myocardial syndrome | ||||||||||||||||||||||||||||
Medical condition: Depression Anxiety Sleep disturbances Circadian disturbances | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
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