- Trials with a EudraCT protocol (211)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
211 result(s) found for: Nasal examination.
Displaying page 1 of 11.
| 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: 2019-004936-52 | Sponsor Protocol Number: CASK0119 | Start Date*: 2020-04-17 |
| Sponsor Name:Cassella-med GmbH & Co KG | ||
| Full Title: Prospective, controlled, randomized double-blind study to determine the sensory perception of two nasal sprays using the model of treatment of post-operative complaints after surgery on the nasal m... | ||
| Medical condition: Post-operative nasal blockage following surgical interventions of the nasal cavity. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (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: 2017-000893-12 | Sponsor Protocol Number: 8302 | Start Date*: 2017-08-31 | |||||||||||||||||||||
| Sponsor Name:The Newcastle Upon Tyne Hospitals NHS Foundation Trust | |||||||||||||||||||||||
| Full Title: Nasal Airway Obstruction Study | |||||||||||||||||||||||
| Medical condition: Deviated Nasal Septum | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2013-003896-37 | Sponsor Protocol Number: BronSin2013 | Start Date*: 2014-01-28 |
| Sponsor Name:URSAPHARM Arzneimittel GmbH | ||
| Full Title: Efficacy and tolerability of Bromelain tablets hysan® in patients with chronic rhinosinusitis. A prospective, double-blind, randomized, placebo-controlled multi-centre trial. A proof of concept stu... | ||
| Medical condition: Patients suffering from chronic rhinosinusitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-002913-37 | Sponsor Protocol Number: MPN-001-07-2018 | Start Date*: 2019-03-13 |
| Sponsor Name:Antibiotic-Razgrad AD | ||
| Full Title: Multicenter, prospective, randomized, double-blind, two-armed phase IV clinical study for efficacy and safety assessment of two 2% mupirocin containing nasal ointments (MupiroNasal 20mg/g, nasal oi... | ||
| Medical condition: For elimination/eradication of nasal carriage of staphylococci, including methicillin-resistant Staphylococcus aureus (MRSA) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BG (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-003004-19 | Sponsor Protocol Number: BILA-2306/ACC | Start Date*: 2006-09-26 | |||||||||||
| Sponsor Name:FAES Farma S.A. | |||||||||||||
| Full Title: A randomised, double-blind, four way cross-over, placebo controlled trial to evaluate the clinical efficacy, onset of action and drug activity at 22-26 hours following the drug intake of Bilastne 2... | |||||||||||||
| Medical condition: Seasonal Allergic Rhinitis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-001510-32 | Sponsor Protocol Number: MP432 | Start Date*: 2006-09-01 | |||||||||||
| Sponsor Name:Meda Pharmaceuticals | |||||||||||||
| Full Title: Active-Controlled Trial of the Safety of MP03-33 in Patients with Chronic Allergic or Nonallergic Rhinitis | |||||||||||||
| Medical condition: Chronic Allergic or Nonallergic Rhinitis | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) SK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-004889-18 | Sponsor Protocol Number: 1.3 | Start Date*: 2022-04-21 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: Effect of Dupilumab in patients with aspirin-exacerbated respiratory disease (AERD) -A single-center prospective pilot study | ||
| Medical condition: Aspirin-exacerbated respiratory disease (AERD), also known as Samter's Triad or Widal's triad, comprises the triad of allergic asthma, chronic rhinosinusitis with nasal polyps (CRswNP) and nonstero... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| 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) | ||
| EudraCT Number: 2004-002807-33 | Sponsor Protocol Number: NLA-C003P | Start Date*: 2004-11-09 |
| Sponsor Name:Biolipox AB | ||
| Full Title: A double blind, randomized, cross-over, placebo controlled study, evaluating the time-to-onset of action of BLX000441-002 nasal spray in healthy volunteers. | ||
| Medical condition: healthy volunteers | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2023-000362-34 | Sponsor Protocol Number: SAN-0791 | Start Date*: 2023-10-12 |
| Sponsor Name:Lek Pharmaceuticals d.d. | ||
| Full Title: An Open-label, Single-Dose, Three-way Crossover Study to Compare the Pharmacokinetics of Fixed-Dose Combination of Mometasone + Azelastine Nasal Spray to Mometasone and Azelastine Nasal Sprays in A... | ||
| Medical condition: Seasonal Allergic Rhinitis | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2009-017997-19 | Sponsor Protocol Number: AGO/2009/014 | Start Date*: 2010-08-25 |
| Sponsor Name:Ghent University Hospital | ||
| Full Title: Influence of oral doxycycline on wound healing after endonasal endoscopic sinus surgery for chronic rhinosinusitis with and without nasal polyposis: a double-blind randomized placebo-controlled trial. | ||
| Medical condition: Chronic rhinosinusitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-004917-10 | Sponsor Protocol Number: P05155 | Start Date*: 2015-03-03 |
| Sponsor Name:Schering-Plough S.A. de C.V. | ||
| Full Title: A Double-Blind Placebo-Controlled, Randomized, Parallel-Group, Multicenter Clinical Trial To Evaluate Efficacy And Safety Of Mometasone Furoate Nasal Spray In Children With Adenoid Hypertrophy. SNO... | ||
| Medical condition: Adenoid Hypertrophy. | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| 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: 2011-001368-23 | Sponsor Protocol Number: MP4000 | Start Date*: 2011-03-30 | ||||||||||||||||
| Sponsor Name:MedPointe Pharmaceuticals | ||||||||||||||||||
| Full Title: Active-Controlled Trial of the Safety and Tolerability of MP29-02 in Subjects with Chronic Allergic or Nonallergic Rhinitis | ||||||||||||||||||
| Medical condition: treatment of chronic allergic or non-allergic rhinitis | ||||||||||||||||||
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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: 2012-002273-54 | Sponsor Protocol Number: ONO-4053POE003 | Start Date*: 2012-11-06 | |||||||||||
| Sponsor Name:Ono Pharmaceutical Co. Ltd. | |||||||||||||
| Full Title: A randomised, double-blind, placebo controlled, double dummy, four period crossover study to evaluate the efficacy, safety and tolerability of oral repeat doses of ONO-4053 and Cetirizine in subjec... | |||||||||||||
| Medical condition: Allergic Rhinitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002726-20 | Sponsor Protocol Number: C-08-32 | Start Date*: 2017-11-07 | |||||||||||
| Sponsor Name:Alcon Research Ltd | |||||||||||||
| Full Title: Safety of PATANASE® Nasal Spray in Patients With Perennial Allergic Rhinitis | |||||||||||||
| Medical condition: Perennial Allergic Rhinitis | |||||||||||||
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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: 2006-000215-22 | Sponsor Protocol Number: HH3104994 | Start Date*: 2006-02-08 |
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
| Full Title: A randomised, double blind, placebo controlled, two-way crossover, three phase, study, to investigate the trial models, Vienna Challenge Chamber, in and out of season, and Park Study in season and ... | ||
| Medical condition: Seasonal Allergic Rhinitis (SAR) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-000654-22 | Sponsor Protocol Number: 13-01/MOM-N | Start Date*: 2013-07-16 | |||||||||||
| Sponsor Name:Dermapharm AG | |||||||||||||
| Full Title: Randomised, double-blind, double-dummy, vehicle controlled parallel trial comparing a novel mometasone furoate nasal spray vs. Nasonex® nasal spray vs. vehicle nasal spray in patients with allergic... | |||||||||||||
| Medical condition: Allergic rhinitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
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