- Trials with a EudraCT protocol (203)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
203 result(s) found for: Nasal congestion.
Displaying page 1 of 11.
EudraCT Number: 2011-002443-10 | Sponsor Protocol Number: 2011035 | Start Date*: 2011-06-23 | |||||||||||
Sponsor Name:Procter & Gamble Technical Centres Ltd., UK | |||||||||||||
Full Title: A Randomized, Open-Label, Single-Dose, Parallel Group Study to Evaluate the Utility of Magnetic Resonance Imaging (MRI) in Demonstrating the Nasal Decongestant Efficacy of an Active Control (Vicks®... | |||||||||||||
Medical condition: Nasal Congestion due to the common cold or hay fever | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001720-36 | Sponsor Protocol Number: BAY E 4465/11764 | Start Date*: 2005-10-24 | |||||||||||
Sponsor Name:BAYER | |||||||||||||
Full Title: A pivotal, placebo controlled, phaseIII study to compare efficacy and tollerability of a fixed combination, containing 500 mg ASA and 30 mg Pseudoephedrine, in comparison to its single components i... | |||||||||||||
Medical condition: Cold related pain/fever e.g. sore throat, headache, ear eache, sinus pressure and nasal congestion. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005155-27 | Sponsor Protocol Number: KCT09/2015-SeptaNazal-Double | Start Date*: 2017-02-22 | |||||||||||
Sponsor Name:Krka, d.d., Novo mesto | |||||||||||||
Full Title: Comparison of the efficacy and safety of the fixed-dose combination of xylometazoline and dexpanthenol in SeptaNazal® and xylometazoline in nasal congestion in patients after surgery in the nose an... | |||||||||||||
Medical condition: Nasal congestion in patients after nasal surgery or nasal cavities surgery and in patients with acute rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SI (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002385-23 | Sponsor Protocol Number: AFT-MXCF-03 | Start Date*: 2015-11-10 | |||||||||||
Sponsor Name:AFT Pharmaceuticals Ltd | |||||||||||||
Full Title: A phase 3 randomised, double blind, multiple dose, parallel group efficacy study of different doses of phenylephrine hydrochloride combined with paracetamol and/or ibuprofen in participants with na... | |||||||||||||
Medical condition: nasal congestion | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004921-41 | Sponsor Protocol Number: P06332 | Start Date*: 2015-02-24 |
Sponsor Name:Corporation Schering-Plough K.K. | ||
Full Title: Multicenter, double-blind, randomized, placebo-controlled study of mometasone furoate nasal spray in pediatric subjects with perennial allergic rhinitis | ||
Medical condition: perennial allergic rhinitis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2004-001637-41 | Sponsor Protocol Number: A7801001 | Start Date*: 2005-07-26 |
Sponsor Name:Pfizer Consumer Healthcare cva/sca | ||
Full Title: A community pharmacy based investigation in the self-medication area Efficacy and safety of Sinutab® (Paracetamol (500mg)/Pseudoephedrine (30mg)) on subjects with nasal congestion accompanied by h... | ||
Medical condition: Medical rationale= Investigation of combination drug Sinutab in symptomatic relief of common cold with nasal symptoms. Community pharmacists are considered as local investigators including subjec... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000058-35 | Sponsor Protocol Number: A7801002 | Start Date*: 2006-04-26 |
Sponsor Name:Pfizer Consumer Healthcare Comm. VA/SCA | ||
Full Title: A community pharmacy based investigation in the self-medication area Efficacy and safety of Sinutab® [Paracetamol (500mg) and Pseudoephedrine (30mg)] on subjects with nasal congestion accompanied ... | ||
Medical condition: The medical rationale = to investigate this combination drug in the symptomatic relief of common cold with nasal symptoms. The reduction of symptom severity may allow subjects receiving active medi... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
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: 2013-001803-35 | Sponsor Protocol Number: ACT12340 | Start Date*: 2013-07-31 | |||||||||||
Sponsor Name:Sanofi-aventis recherche et développement | |||||||||||||
Full Title: A Randomized, Double-Blind, Phase 2, Placebo Controlled, 2 Arm Study To Evaluate Dupilumab In Patients With Bilateral Nasal Polyposis And Chronic Symptoms Of Sinusitis | |||||||||||||
Medical condition: Nasal polyps | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) SE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005006-66 | Sponsor Protocol Number: 2013118 | Start Date*: 2014-01-21 |
Sponsor Name:Procter and Gamble | ||
Full Title: A 2-arm, randomised, single - (Investigator) blind, controlled, parallel design study in common cold sufferers experiencing nasal congestion to assess the speed of action of Vicks® VapoRub® (VVR) | ||
Medical condition: Nasal congestion due to common cold in adults | ||
Disease: | ||
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 |
EudraCT Number: 2014-004918-28 | Sponsor Protocol Number: P05528 | Start Date*: 2015-02-24 |
Sponsor Name:Schering-Plough Research Institute, a Division of Schering Corporation | ||
Full Title: PLACEBO-CONTROLLED STUDY OF MOMETASONE FUROATE NASAL SPRAY (MFNS) 200 MCG QD IN THE RELIEF OF NASAL CONGESTION ASSOCIATED WITH SEASONAL ALLERGIC RHINITIS (SAR) (Protocol No. P05528) | ||
Medical condition: Seasonal Allergic Rhinitis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2017-002154-36 | Sponsor Protocol Number: CIGE025F1301 | Start Date*: 2019-02-13 | ||||||||||||||||
Sponsor Name:Novartis Pharma KK | ||||||||||||||||||
Full Title: A 12 Week, Multi-center, Randomized, Double-blind, Placebo-controlled Phase III Study to Evaluate the Efficacy and Safety of Omalizumab in Adult and Adolescent Patients With Inadequately Controlled... | ||||||||||||||||||
Medical condition: Severe Japanese cedar pollinosis | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003101-42 | Sponsor Protocol Number: EFC14146 | Start Date*: 2016-11-18 | |||||||||||
Sponsor Name:SANOFI-AVENTIS RECHERCHE ET DEVELOPPEMENT | |||||||||||||
Full Title: A Randomized, 24-Week Treatment, Double-blind, Placebo-controlled Efficacy and Safety Study of Dupilumab Every Other Week, in Patients with Bilateral Nasal Polyposis on a Background Therapy with In... | |||||||||||||
Medical condition: nasal polyps | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) DE (Completed) NL (Completed) CZ (Completed) FR (Completed) PL (Completed) BG (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001314-10 | Sponsor Protocol Number: EFC14280 | Start Date*: 2016-11-29 | |||||||||||
Sponsor Name:SANOFI-AVENTIS RECHERCHE ET DEVELOPPEMENT | |||||||||||||
Full Title: A Randomized, Double-blind, 52-week, Placebo Controlled Efficacy and Safety Study of Dupilumab, in Patients with Bilateral Nasal Polyposis on a Background Therapy with Intranasal Corticosteroids | |||||||||||||
Medical condition: Bilateral nasal polyposis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) PT (Completed) ES (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004920-23 | Sponsor Protocol Number: P05583 | Start Date*: 2015-02-24 |
Sponsor Name:Schering-Plough Research Institute, a Division of Schering Corporation | ||
Full Title: PLACEBO-CONTROLLED STUDY OF MOMETASONE FUROATE NASAL SPRAY (MFNS) 200 MCG QD IN THE RELIEF OF NASAL CONGESTION ASSOCIATED WITH SEASONAL ALLERGIC RHINITIS (SAR) (Protocol No. P05583) | ||
Medical condition: SEASONAL ALLERGIC RHINITIS | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2014-004919-36 | Sponsor Protocol Number: P05529 | Start Date*: 2015-02-24 |
Sponsor Name:Schering-Plough Research Institute, a Division of Schering Corporation | ||
Full Title: PLACEBO-CONTROLLED STUDY OF MOMETASONE FUROATE NASAL SPRAY (MFNS) 200 MCG QD IN THE RELIEF OF NASAL CONGESTION ASSOCIATED WITH SEASONAL ALLERGIC RHINITIS (SAR) | ||
Medical condition: SEASONAL ALLERGIC RHINITIS (SAR) | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2018-002073-22 | Sponsor Protocol Number: CQAW039A2322 | Start Date*: 2018-12-13 | ||||||||||||||||
Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
Full Title: A multicenter, randomized, double-blind, parallel-group, placebo-controlled study of fevipiprant once daily plus standard-of-care (SoC) for assessment of the efficacy in reduction of nasal polyps s... | ||||||||||||||||||
Medical condition: Nasal polyposis in patients with concomitant asthma. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) NL (Completed) CZ (Completed) BE (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000460-42 | Sponsor Protocol Number: AK001-002 | Start Date*: 2016-06-29 | |||||||||||
Sponsor Name:Allakos, Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo Controlled, Study to Evaluate Multiple Doses of AK001 in Patients With Moderate to Severe Nasal Polyposis | |||||||||||||
Medical condition: Moderate to severe nasal polyposis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Prematurely Ended) ES (Completed) NL (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000684-10 | Sponsor Protocol Number: ME3301-12 | Start Date*: 2004-10-28 |
Sponsor Name:Meiji Seika Kaisha, Ltd. | ||
Full Title: A randomised, double-blind, placebo-controlled crossover study to investigate the efficacy and safety of three doses of ME3301 in patients with seasonal allergic rhinitis during allergen challenge ... | ||
Medical condition: seasonal allergic rhinitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
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