- Trials with a EudraCT protocol (420)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (133)
420 result(s) found for: nose.
Displaying page 1 of 21.
EudraCT Number: 2016-001530-10 | Sponsor Protocol Number: NoPac01 | Start Date*: 2017-02-20 | |||||||||||
Sponsor Name:Royal Devon & Exeter NHS Foundation Trust | |||||||||||||
Full Title: A randomised controlled trial of topical intranasal tranexamic acid versus placebo to reduce the need for nasal packing in patients presenting to the Emergency Department with spontaneous epistaxis. | |||||||||||||
Medical condition: Atraumatic epistaxis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (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: 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: 2005-004959-35 | Sponsor Protocol Number: GrassMATAMPL301 | Start Date*: 2006-09-11 |
Sponsor Name:Allergy Therapeutics (UK) Ltd | ||
Full Title: Efficacy and Safety/Tolerability of GrassMATAMPL, a Randomized, Placebo-Controlled, Double-Blind Study | ||
Medical condition: Type I respiratory hypersensitivity to cross-reacting grass pollens | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000075-33 | Sponsor Protocol Number: SINTART1 | Start Date*: 2013-05-04 | |||||||||||
Sponsor Name:Fondazione IRCCS Istituto Nazionale Tumori | |||||||||||||
Full Title: Multidisciplinary approach for poor prognosis sinonasal tumors: Phase II study of chemotherapy, surgery, photon and heavy ion radiotherapy integration for more effective and less toxic treatment in... | |||||||||||||
Medical condition: Poor prognosis sinonasal tumors in operable patients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005215-42 | Sponsor Protocol Number: KloMid02 | Start Date*: 2013-04-12 |
Sponsor Name:Department of Anesthesiology and Intensive Care Medicine | ||
Full Title: Children's mood/anxiety, pain, nausea and behavioral changes after premedication with Clonidine versus Midazolam in ENT day surgery. | ||
Medical condition: Preanesthetic Medication at ear-nose-throat surgery | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000580-93 | Sponsor Protocol Number: SINTART2 | Start Date*: 2013-05-04 | |||||||||||
Sponsor Name:Fondazione IRCCS Istituto Nazionale Tumori | |||||||||||||
Full Title: Multidisciplinary approach for poor prognosis sinonasal tumors: Phase II study of chemotherapy, photon and heavy ion radiotherapy integration for more effective and less toxic treatment in inoperab... | |||||||||||||
Medical condition: Poor prognosis inoperable sinonasal tumors. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2012-001591-11 | Sponsor Protocol Number: 3.4.11.049 | Start Date*: 2012-12-21 |
Sponsor Name:Erasmus MC | ||
Full Title: Symptomatic treatment of pollen related allergic rhinoconjunctivitis and the relation with asthma with children in the General practice | ||
Medical condition: Allergic Rhinitis Asthma | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
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: 2020-001721-31 | Sponsor Protocol Number: SPON-AK-0420 | Start Date*: 2020-05-01 | |||||||||||
Sponsor Name:Hampshire Hospitals NHS TRust | |||||||||||||
Full Title: Can a sinus rinse and mouth wash reduce viral load in COVID-19 positive individuals? | |||||||||||||
Medical condition: Covid-19 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004183-29 | Sponsor Protocol Number: DERC-03 | Start Date*: 2014-06-27 | |||||||||||
Sponsor Name:Dermal Laboratories | |||||||||||||
Full Title: A randomised, placebo-controlled trial to investigate the effectiveness of an antimicrobial product in the elimination of Staphylococcus aureus colonisation from the anterior nares of adult subject... | |||||||||||||
Medical condition: Nasal colonisation with Staphylococcus aureus | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
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: 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: 2016-004827-22 | Sponsor Protocol Number: BM41-VD3 | Start Date*: 2017-07-25 |
Sponsor Name:Academic Medical Center | ||
Full Title: A randomized, double-blind, placebo-controlled, double-dummy study to determine the safety/tolerability of a simultaneous subcutaneous treatment of BM41 and vitamin D 3 in patients with moderate to... | ||
Medical condition: moderate to severe allergic rhinitis/rhino-conjunctivitis caused by birch pollen (with or without concomitant mild to moderate persistent asthma) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003846-26 | Sponsor Protocol Number: C-05-69 | Start Date*: 2017-11-19 | |||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||
Full Title: Safety Study of Olopatadine Nasal Spray | |||||||||||||
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: 2005-002805-21 | Sponsor Protocol Number: D2530C00011 | Start Date*: 2005-09-25 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A randomized, double-blind, placebo controlled, three-way crossover study exploring the efficacy of AZD3778 compared with placebo and an oral antihistamine (loratadine) in a model of seasonal aller... | ||
Medical condition: This is a Phase II trial (Proof of Principle) in volunteer rhinitis subjects utilising a seasonal model of rhinitis and challenge agent | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (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: 2013-002414-12 | Sponsor Protocol Number: 12082.101 | Start Date*: Information not available in EudraCT |
Sponsor Name:PARI Pharma GmbH | ||
Full Title: A randomised, open, controlled pilot study to investigate the efficacy and safety of Buparid/PARI SINUS versus Budes® Nasal Spray in the therapy of Chronic Rhinosinusitis (CRS) with polyposis nasi ... | ||
Medical condition: Chronic Rhinosinusitis (CRS) with polyposis nasi | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004730-18 | Sponsor Protocol Number: OSLER_TIMOLOL | Start Date*: 2019-12-11 | |||||||||||
Sponsor Name:University Hospital Regensburg | |||||||||||||
Full Title: The influence of Timolol Nasal Spray on Epistaxis in Hereditary Hemorrhagic Telangiectasia (HHT) | |||||||||||||
Medical condition: 2) hereditary hemorrhagic telangiectasia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
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