- Trials with a EudraCT protocol (106)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5)
106 result(s) found for: Apnea.
Displaying page 1 of 6.
EudraCT Number: 2015-003095-68 | Sponsor Protocol Number: ORL-DISE-2015 | Start Date*: 2016-04-29 | |||||||||||
Sponsor Name:Fundació Parc Taulí | |||||||||||||
Full Title: Randomized cross-over open-label clinical trial to compare the videoendoscopic examination with induced sleep after sedation with propofol or clonidine | |||||||||||||
Medical condition: Apnea hypopnea syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006220-35 | Sponsor Protocol Number: 118/2007/O/Sper | Start Date*: 2008-06-03 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Efficacy of Oral Leukotriene in long term therapy of mild and moderate obstructive sleep apnea syndrome (OSAS) in children. | |||||||||||||
Medical condition: obstructive sleep apnea syndrome | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002174-58 | Sponsor Protocol Number: ACT6796 | Start Date*: 2007-11-30 | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled, study of the safety and activity of four escalating single doses of AVE0657 in patients suffering from Obstructive Sleep Apnea Hypopnea Syndrome | |||||||||||||
Medical condition: Patients suffering from Obstructiv-Sleep Apnea Hypopnea Syndrome (OSAHS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) ES (Completed) DE (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: 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: 2019-004917-15 | Sponsor Protocol Number: RebOx | Start Date*: 2020-04-22 | |||||||||||
Sponsor Name:ISTITUTO AUXOLOGICO ITALIANO | |||||||||||||
Full Title: Crossover, Double-blind, Phase 2 Study of a Fixed Dose Combination of Reboxetine\Oxybutynin (AD128) Versus Placebo in Obstructive Sleep Apnea (RebOx) | |||||||||||||
Medical condition: Obstructive Sleep Apnea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003930-28 | Sponsor Protocol Number: 15-004 | Start Date*: 2018-10-09 | |||||||||||
Sponsor Name:Jazz Pharmaceuticals Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Crossover On-Road Driving Study Assessing the Effect of JZP-110 on Driving Performance in Subjects with Excessive sleepiness Due to Obstructive Sleep... | |||||||||||||
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) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003119-39 | Sponsor Protocol Number: 38RC15.175 | Start Date*: 2015-10-29 | ||||||||||||||||
Sponsor Name:Centre Hospitalier Universitaire de Grenoble | ||||||||||||||||||
Full Title: effects of a short therpay of zolpidem with support servo-ventilation versus placebo in patients with central sleep apnea with chronic heart failure | ||||||||||||||||||
Medical condition: chronic heart failure and central sleep apnea | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
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: 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: 2021-002926-26 | Sponsor Protocol Number: STM-042/K | Start Date*: 2021-11-15 | |||||||||||
Sponsor Name:Desitin Arzneimittel GmbH | |||||||||||||
Full Title: Efficacy, Safety and Tolerability of 3 doses of Sulthiame in Patients with Obstructive Sleep Apnea. A Randomized, Double-Blind, Placebo Controlled, Dose-Ranging Study | |||||||||||||
Medical condition: Obstructive sleep apnea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Ongoing) CZ (Completed) FR (Completed) DE (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: 2005-000733-37 | Sponsor Protocol Number: 21402 | Start Date*: 2005-08-20 | |||||||||||
Sponsor Name:NV Organon | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multicenter parallel-group dose ranging clinical trial to assess the efficacy and safety of Org 4419-2 in the treatment of obstructive sleep apnea/hy... | |||||||||||||
Medical condition: Obstructive sleep apnea/hypopnea syndrome | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004539-36 | Sponsor Protocol Number: 16NC06 | Start Date*: 2020-05-19 | ||||||||||||||||
Sponsor Name:Great Ormond Street Hospital for Children NHS Foundation Trust | ||||||||||||||||||
Full Title: Study of Montelukast In Children with Sickle Cell Disease (SMILES) | ||||||||||||||||||
Medical condition: Sleep-disordered breathing | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001459-23 | Sponsor Protocol Number: D Box 2008/0000 | Start Date*: 2008-06-24 | ||||||||||||||||
Sponsor Name:Nikolai Sleep Monitoring Clinic | ||||||||||||||||||
Full Title: Treatment of Testosterone deficiency in men with Sleep Apnoea Syndrome utilising Nebido therapy. | ||||||||||||||||||
Medical condition: Sleep Apnoea Hypogonadism- testosterone deficiency syndrome | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003029-83 | Sponsor Protocol Number: OSAS_UCBH | Start Date*: 2020-12-03 | |||||||||||
Sponsor Name:Service de Neurologie, CHU Liège | |||||||||||||
Full Title: Assessment of changes in regional brain synaptic density in patients with Obstructive Sleep Apnea (OSA) measured by positron emission tomography and 18F-UCB-H. | |||||||||||||
Medical condition: Obstructive sleep apnea syndrome | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
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: 2010-018892-20 | Sponsor Protocol Number: HDZKA-2010-01 | Start Date*: 2010-07-08 | |||||||||||
Sponsor Name:Herz- & Diabeteszentrum NRW | |||||||||||||
Full Title: Pathophysiologie der Cheyne-Stokes Atmung: Senkung des pulmonalkapillären Wedge-Drucks als kausaler Therapieansatz | |||||||||||||
Medical condition: Cheyne-Stokes respiration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019413-25 | Sponsor Protocol Number: P09-16/BF2.649 | Start Date*: 2010-06-28 | |||||||||||
Sponsor Name:Bioprojet | |||||||||||||
Full Title: Minimum effective dose-finding study of BF2.649, in patients with moderate to severe Obstructive Sleep Apnea, experiencing Excessive Daytime Sleepiness (EDS) despite regular use of nCPAP, and patie... | |||||||||||||
Medical condition: Treatment of excessive daytime sleepiness associated to obstructive sleep apnea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (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 |
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