- Trials with a EudraCT protocol (13)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
13 result(s) found for: Decongestants.
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EudraCT Number: 2019-003254-91 | Sponsor Protocol Number: AGO/2019/005 | Start Date*: 2020-08-18 |
Sponsor Name:Ghent University Hospital | ||
Full Title: Characterisation and intervention study in patients with long-term use of nasal decongestants. | ||
Medical condition: rhinitis medicamentosa | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: View results |
EudraCT Number: 2018-000065-37 | Sponsor Protocol Number: DOSA_Protocol | Start Date*: 2019-01-30 | ||||||||||||||||
Sponsor Name:University of Oxford | ||||||||||||||||||
Full Title: Randomised controlled trial of nasal decongestants versus placebo to prolong treatment free periods from continuous positive airway pressure therapy in mild to moderate obstructive sleep apnoea | ||||||||||||||||||
Medical condition: Obstructive Sleep Apnoea Syndrome | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Temporarily Halted) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-000215-31 | Sponsor Protocol Number: S65796 | Start Date*: 2022-05-24 | |||||||||||
Sponsor Name:UZ Leuven | |||||||||||||
Full Title: A monocentric academic trial comparing the diagnostic value of history taking and nasal lysine aspirin provocation test in the diagnosis of AERD in CRSwNP patients | |||||||||||||
Medical condition: Aspirin-Exacerbated Respiratory Disease (AERD) in patients with Chronic RhinoSinusitis with Nasal Polyps (CRSwNP) | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001548-36 | Sponsor Protocol Number: pulmozyme-nasal-cf | Start Date*: Information not available in EudraCT |
Sponsor Name:University of Jena | ||
Full Title: Nasale Inhalation von Pulmozyme bei Patienten mit Mukoviszidose und chronischer Rhinosinusitis mit dem Pari Sinus-Vernebler. - bizentrische, randomisierte, doppel-blinde, placebo-kontrollierte, pr... | ||
Medical condition: Cystic Fibrosis with chronic rhinosinusitis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-000421-76 | Sponsor Protocol Number: AirGOs-biologics | Start Date*: 2020-04-15 |
Sponsor Name:Helsinki University Hospital | ||
Full Title: Aggravated airway inflammation: research on biological treatment (Mepolizumab) AirGOs-biologics | ||
Medical condition: A triad of chronic rhinosinusitis with nasal polyps (CRSwNP), asthma and NSAID exacerbated respiratory disease (NERD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005035-85 | Sponsor Protocol Number: 2012RC14 | Start Date*: 2013-05-03 | |||||||||||
Sponsor Name:Tayside Medical Sciences Centre on behalf of University of Dundee & NHS Tayside | |||||||||||||
Full Title: A proof of concept study in allergic rhinitis, to evaluate the differential effects of doxazosin between single and chronic dosing on nasal airway calibre | |||||||||||||
Medical condition: Allergic Rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002134-74 | Sponsor Protocol Number: FLU-v004 | Start Date*: 2016-07-27 | |||||||||||
Sponsor Name:PepTcell Limited (trade name SEEK) | |||||||||||||
Full Title: Phase IIb Study of the Efficacy of FLU-v, a Broad Spectrum Influenza Vaccine in an H1N1 Influenza Healthy Human Challenge Model | |||||||||||||
Medical condition: Influenza virus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005207-42 | Sponsor Protocol Number: 2005079 | Start Date*: 2005-12-29 | |||||||||||
Sponsor Name:Procter & Gamble Technical Centres Limited | |||||||||||||
Full Title: A study to assess the efficacy of a combination of natural plant extracts in natural colds. | |||||||||||||
Medical condition: Common Cold (nasopharyngitis), Upper Respiratory Tract Infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000368-12 | Sponsor Protocol Number: OPN-FLU-CS-3205 | Start Date*: 2019-10-01 | |||||||||||
Sponsor Name:OptiNose US, Inc. | |||||||||||||
Full Title: A 24-Week Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter Study Evaluating the Efficacy and Safety of Intranasal Administration of 186 and 372 μg of OPN-375 Twice a Day (... | |||||||||||||
Medical condition: Chronic sinusitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001869-16 | Sponsor Protocol Number: BRN-C-2013-02 | Start Date*: 2013-09-24 | |||||||||||
Sponsor Name:Boiron Laboratoires | |||||||||||||
Full Title: A randomised, multi-centre, parallel group, double-blind, placebo-controlled study to assess the efficacy and safety of Oscillococcinum® in the treatment of symptoms of Influenza-like illness (ILI) | |||||||||||||
Medical condition: Systemic and respiratory symptoms of Influenza-like-illness (ILI) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000648-86 | Sponsor Protocol Number: OPN-FLU-CS-3206 | Start Date*: 2019-10-01 | |||||||||||
Sponsor Name:OptiNose US, Inc. | |||||||||||||
Full Title: A 24-Week Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter Study Evaluating the Efficacy and Safety of Intranasal Administration of 186 and 372 μg of OPN-375 Twice a Day (B... | |||||||||||||
Medical condition: Chronic rhinosinusitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) PL (Completed) ES (Ongoing) BG (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004887-31 | Sponsor Protocol Number: OPN-FLU-NP-3102 | Start Date*: 2014-11-04 | |||||||||||
Sponsor Name:OptiNose US, Inc | |||||||||||||
Full Title: A 16-Week RaNdomized, Double-Blind, Placebo-Controlled, PArallel-Group, Multicenter Study EValuatInG the Efficacy and Safety of Intranasal Administration of 100, 200, and 400 μg of FluticAsone Prop... | |||||||||||||
Medical condition: Bilateral Nasal Polyposis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004886-34 | Sponsor Protocol Number: OPN-FLU-NP-3101 | Start Date*: 2014-03-26 | |||||||||||
Sponsor Name:OptiNose US, Inc | |||||||||||||
Full Title: A 16-Week RaNdomized, Double-Blind, Placebo-Controlled, PArallel-Group, Multicenter Study EValuatInG the Efficacy and Safety of Intranasal Administration of 100, 200, and 400 μg of FluticAsone Prop... | |||||||||||||
Medical condition: Bilateral Nasal Polyposis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
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