- Trials with a EudraCT protocol (57)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
57 result(s) found for: Nasal provocation test.
Displaying page 1 of 3.
EudraCT Number: 2014-001088-11 | Sponsor Protocol Number: s56489 | Start Date*: 2014-07-29 |
Sponsor Name:MEDA | ||
Full Title: Academic study on the effects of MP 29-02 nasal spray on inflammatory mediators in allergic rhinitis | ||
Medical condition: Allergic rhinitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
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: 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 (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-005079-21 | Sponsor Protocol Number: LOTAB_2b_HDM | Start Date*: 2018-08-23 | |||||||||||
Sponsor Name:Lofarma S.p.A. | |||||||||||||
Full Title: A Prospective, Multicenter, Double-Blind, Placebo-Controlled, Dose-Finding Phase-II Study for the Efficacy and Safety of LAIS® House Dust Mites Sublingual Tablets in Patients with Mite-Induced Alle... | |||||||||||||
Medical condition: Patients Suffering from Mite-Induced Allergic Rhino-Conjunctivitis Without or With Controlled Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001611-50 | Sponsor Protocol Number: S67072 | Start Date*: 2022-11-15 | |||||||||||
Sponsor Name:UZ Leuven | |||||||||||||
Full Title: Patient reported efficacy of intranasal lysine-aspirin in controlling NSAID-exacerbated respiratory disease | |||||||||||||
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 (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004830-32 | Sponsor Protocol Number: ICPCT-2011-UA-FF | Start Date*: 2012-01-27 | |||||||||||
Sponsor Name:FAES FARMA, S.A. | |||||||||||||
Full Title: Effects of bilastine on nasal volume after allergen-induced rhinitis in patients with allergic rhinitis | |||||||||||||
Medical condition: Allergic Rhinitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003119-21 | Sponsor Protocol Number: 1 | Start Date*: 2017-12-22 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Effect of Omalizumab in patients with Aspirin-Exazerbated Respiratory Disease (AERD) | ||
Medical condition: Aspirin-exacerbated respiratory disease (AERD), also known as Samter's triad or Widal's triad, comprises the triad of Asthma, chronic rhinosinusitis with nasal polyps (CRwNP) and nonsteroidal anti-... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000597-29 | Sponsor Protocol Number: 2017-02-CHRMT | Start Date*: 2021-06-02 |
Sponsor Name:Centre Hospitalier Régional Metz-Thionville | ||
Full Title: Interest of Nasal Provocation Tests for Diagnosis of House Mites Allergic Rhinitis | ||
Medical condition: mite allergenic rhinitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002944-18 | Sponsor Protocol Number: BIA-HDMP-201 | Start Date*: 2016-11-14 |
Sponsor Name:Bial Industrial Farmacéutica S.A. | ||
Full Title: MULTICENTRE, RANDOMIZED, DOUBLE BLIND CLINICAL TRIAL PHASE II, WITH SUBCUTANEOUS POLYMERIZED DEPOT IMMUNOTHERAPY AT DIFFERENT DOSES IN PARALLEL PLACEBO-CONTROLLED GROUPS IN PATIENTS WITH ALLERGIC R... | ||
Medical condition: The disease under study is allergic rhinoconjunctivitis secondary to sensitization to DPT and DF. Included in the study are patients diagnosed with that disease who also have associated mild asthma... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016815-39 | Sponsor Protocol Number: il-ASIT1 | Start Date*: 2010-01-15 |
Sponsor Name:Allergy Unit Department of Oto-rhino-Laryngology Lund/Malmö University Hospital | ||
Full Title: Is Intralymphatic Allergen Immunotherapy effective and safe: A human randomized clinical trial | ||
Medical condition: Seasonal Allergic rhinitis due to pollen from grass and betula verrucosa | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005420-17 | Sponsor Protocol Number: CC10-200601 | Start Date*: 2007-01-23 |
Sponsor Name:LTB4 Sweden AB | ||
Full Title: A double-blind, randomised, placebo-controlled, crossover, allergen challenge study, evaluating the safety, tolerability and effects of intranasal administration of recombinant human Clara Cell 10 ... | ||
Medical condition: The study is a proof-of-concept study with the objective to investigate whether rhCC10, administered intranasally, can affect the response to an allergen provocation test in subjects with allergic ... | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004214-96 | Sponsor Protocol Number: MEIN/15/Bil-PSR/002 | Start Date*: 2017-02-02 | |||||||||||
Sponsor Name:MENARINI INTERNATIONAL OPERATIONS LUXEMBOURG SA | |||||||||||||
Full Title: Bilastine and inflammation: an explorative study in subjects affected by Parietaria J.-induced Rhinoconjunctivitis – The Bi-FLO study | |||||||||||||
Medical condition: Rhinoconjunctivitis induced by Parietaria J. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003067-31 | Sponsor Protocol Number: 600-PG-PSC-156 | Start Date*: 2006-09-25 | |||||||||||
Sponsor Name:LETI Pharma GmbH | |||||||||||||
Full Title: A randomized, double blinded, placebo controlled multicenter study for the efficacy and safety of Depigoid® tree pollen | |||||||||||||
Medical condition: Rhinitis and/or rhinoconjunctivitis with or without allergic asthma caused by clinical relevant sensitization against tree pollen. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001259-63 | Sponsor Protocol Number: Pollenvaccine2014-01-15 | Start Date*: 2016-03-09 |
Sponsor Name:Department of Clinical Science, Intervention and Technology, Karolinska Institute | ||
Full Title: Intralymphatic immunotherapy in increasing doses up to 10 000 SQ-U -a human randomized clinical trial | ||
Medical condition: Patients with severe to moderate Allegic rhinitis. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002317-10 | Sponsor Protocol Number: SC-31A | Start Date*: 2019-04-17 | |||||||||||||||||||||
Sponsor Name:ROXALL Medizin GmbH | |||||||||||||||||||||||
Full Title: Phase II study to assess the tolerability, safety and efficacy of subcutaneous cluster-immunotherapy in patients suffering from house dust mite allergy | |||||||||||||||||||||||
Medical condition: Allergic rhinitis / rhino-conjunctivitis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000683-27 | Sponsor Protocol Number: GRAY09 | Start Date*: 2006-05-17 |
Sponsor Name:Research and Innovation Services | ||
Full Title: A Placebo Controlled Trial to Evaluate The Effects of Levocetirizine on Nasal Allergen Challenge And Adenosine Monophosphate Challenge In Patients with Intermittent and Persistent Allergic Rhinitis | ||
Medical condition: Allergic Rhinitis - Both Persistent and Intermittent | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
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: 2008-003879-49 | Sponsor Protocol Number: AB0802 | Start Date*: 2009-03-27 |
Sponsor Name:Artu Biologicals Europe B.V. | ||
Full Title: A double-blind, randomised, placebo controlled, phase I/IIa dose escalation study to investigate the safety and the effect of different doses of Oralgen House Dust Mite in patients with house dust ... | ||
Medical condition: Treatment of house dust mite induced allergic rhinoconjunctivitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2017-005038-53 | Sponsor Protocol Number: FIM-PRU-2018-01 | Start Date*: 2019-05-16 | |||||||||||
Sponsor Name:Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina Y Salud (FIMABIS) | |||||||||||||
Full Title: Randomized double-blind, placebo-controlled study evaluate the efficacy and mechanisms involved in immunotherapy Sublingual specifies with Pru p 3 (Pru p 3-ITSL) in patients with allergy to nsLTP w... | |||||||||||||
Medical condition: LTP syndrome. | |||||||||||||
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Population Age: Children, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011999-30 | Sponsor Protocol Number: VO64.08 | Start Date*: 2009-09-16 | |||||||||||
Sponsor Name:Stallergenes S.A. | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, multi-national, Phase III trial to assess the efficacy and safety of 300 IR sublingual immunotherapy (SLIT) administered as allergen-based tablets on... | |||||||||||||
Medical condition: House Dust Mite Allergic Rhinitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) ES (Prematurely Ended) HU (Completed) DE (Prematurely Ended) FR (Completed) DK (Prematurely Ended) SK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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