- Trials with a EudraCT protocol (423)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (362)
423 result(s) found for: Rhinitis.
Displaying page 1 of 22.
EudraCT Number: 2007-003291-19 | Sponsor Protocol Number: VAI01 | Start Date*: 2009-07-30 | ||||||||||||||||
Sponsor Name:University of Dundee | ||||||||||||||||||
Full Title: A proof of concept study to evaluate if concomitant topical intranasal steroid prevents tolerance and rebound congestion due to regular oxymetazoline in persistent allergic rhinitis | ||||||||||||||||||
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: 2006-006379-19 | Sponsor Protocol Number: IGG-GIRO-001 | Start Date*: 2007-05-08 | |||||||||||
Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
Full Title: Evaluation of a treatment with levocetirizine in children allergic to mites suffering for recurrent respiratory infections with or without concomitant asthma symptoms | |||||||||||||
Medical condition: persistent allergic rhinitis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003058-26 | Sponsor Protocol Number: ModAll-Der/07 | Start Date*: 2007-07-17 | |||||||||||
Sponsor Name:LOFARMA | |||||||||||||
Full Title: Pilot study on tolerability of specific immunotherapywith injective allergoid adsorbed on calcium phosphate in patients with respiratory allergy to house dust mite. | |||||||||||||
Medical condition: allergic rhinoconjunctivitis with or without asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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: 2007-006099-12 | Sponsor Protocol Number: TSO-01 | Start Date*: 2007-12-21 | |||||||||||
Sponsor Name:Statens Serum Institut | |||||||||||||
Full Title: Oral treatment of allergy with a non-pathogenic microorganism: A randomised clinical trial | |||||||||||||
Medical condition: Allergic rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021361-69 | Sponsor Protocol Number: DC01/RUP/2/09 | Start Date*: 2010-09-13 | |||||||||||
Sponsor Name:J. Uriach y Compañía, S.A. | |||||||||||||
Full Title: A multicenter, open-label study to assess pharmacokinetics, efficacy, tolerability and safety of Rupatadine in paediatrics patients (2-5 years old) with allergic rhinitis. | |||||||||||||
Medical condition: Allergic Rhinitis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004642-32 | Sponsor Protocol Number: 2007ENT03 | Start Date*: 2008-10-10 | |||||||||||
Sponsor Name:University of East Anglia | |||||||||||||
Full Title: THE EFFECT OF THEOPHYLLINE IN PATIENTS WITH RHINITIS | |||||||||||||
Medical condition: Rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001179-30 | Sponsor Protocol Number: OX914-001 | Start Date*: 2008-06-30 | |||||||||||
Sponsor Name:Orexo AB | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled, cross-over, allergen challenge study to evaluate the efficacy, safety and tolerability of BLX-028914 in subjects with allergic rhinitis | |||||||||||||
Medical condition: Allergic rhinitis (LLT) Code 10001723 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003970-16 | Sponsor Protocol Number: C-07-02 | Start Date*: 2017-11-22 | |||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||
Full Title: Safety and Pharmacokinetics of PATANASE in Paediatric Patients 2 to < 6 Years of Age with a history of allergic rhinitis | |||||||||||||
Medical condition: Allergic rhinitis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002277-38 | Sponsor Protocol Number: MT-06 | Start Date*: 2011-10-06 | |||||||||||||||||||||
Sponsor Name:ALK-Abelló A/S | |||||||||||||||||||||||
Full Title: A one-year trial evaluating the efficacy and safety of the ALK house dust mite allergy immunotherapy tablet in adult subjects with house dust mite allergic rhinitis | |||||||||||||||||||||||
Medical condition: allergic rhinitis | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) CZ (Completed) LV (Completed) DK (Completed) AT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-004820-35 | Sponsor Protocol Number: GT17 Italy | Start Date*: 2007-05-15 | |||||||||||
Sponsor Name:ALK-ABELLO | |||||||||||||
Full Title: Multicenter, randomized, parallel groups, semi-cross over, open Phase IIIB trial to evaluate treatment compliance for subglossal specific Immunotherapy oral lyophilisate tablets GrazaxR in patien... | |||||||||||||
Medical condition: Allergic rhinoconjunctivitis caused by grass pollen | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006787-11 | Sponsor Protocol Number: 0819D1522 | Start Date*: 2009-01-15 | |||||||||||
Sponsor Name:Shionogi & Co., Ltd. | |||||||||||||
Full Title: A randomized, double blind, placebo-controlled, 2-period cross over study to evaluate effects of S-555739 on prostaglandin D2 (PGD2) induced nasal airway resistance in healthy adult volunteers | |||||||||||||
Medical condition: Allergic rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001728-20 | Sponsor Protocol Number: AV-X-02 | Start Date*: 2013-11-13 | |||||||||||
Sponsor Name:ALK-Abelló S. A. | |||||||||||||
Full Title: An open trial to assess the tolerability of AVANZ® Salsola immunotherapy | |||||||||||||
Medical condition: Allergic rhinoconjunctivitis with or without asthma due to sensitisation to Salsola kali pollen | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004720-11 | Sponsor Protocol Number: AV-X-03 | Start Date*: 2014-02-11 | |||||||||||
Sponsor Name:ALK-Abelló, S.A. | |||||||||||||
Full Title: An open trial to assess the tolerability of AVANZ® Cupressus immunotherapy | |||||||||||||
Medical condition: Allergic rhinoconjunctivitis induced by Cupressus arizonica pollen. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003108-20 | Sponsor Protocol Number: DM04RUP/IV/05 | Start Date*: 2006-11-29 | |||||||||||
Sponsor Name:URIACH J. URIACH Y COMPANIA S.A. | |||||||||||||
Full Title: A DOUBLE BLIND, RANDOMISED, PARALLEL, PLACEBO-CONTROLLED, PILOT STUDY TO EVALUATE THE ANTI-INFLAMMATORY EFFECTS AND THE EFFICACY OF RUPATADINE 10 MG ON THE SYMPTOMS OF PERSISTENT ALLERGIC RHINITIS | |||||||||||||
Medical condition: PAR | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004031-40 | Sponsor Protocol Number: Version3.22.11.2014 | Start Date*: 2015-04-30 | |||||||||||
Sponsor Name:Department of Respiratory Diseases, Aarhus University Hospital | |||||||||||||
Full Title: Training in intralymphatically injection technique. A realistic learning study | |||||||||||||
Medical condition: allergic rhino-conjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005263-26 | Sponsor Protocol Number: GT-16 | Start Date*: 2006-12-19 | |||||||||||
Sponsor Name:ALK-Abelló, S.A. | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled Phase IIIb Study investigating changes in immunological parameters and cutaneous reactivity induced by a short course immunotherapy with ALK grass tab... | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004852-20 | Sponsor Protocol Number: AV-X-01 | Start Date*: 2012-04-10 | |||||||||||
Sponsor Name:ALK-Abelló, S.A. | |||||||||||||
Full Title: An open trial to assess the tolerability of AVANZ Olive immunotherapy | |||||||||||||
Medical condition: Allergic rhinoconjunctivitis with/without asthma due to sensitization to Olea europaea (olive) pollen | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001457-16 | Sponsor Protocol Number: RINKAST | Start Date*: 2005-09-06 | |||||||||||
Sponsor Name:UNIVERSITA' DEGLI STUDI DI UDINE | |||||||||||||
Full Title: RANDOMIZED, DOUBLE BLIND TRIAL MONTELUKAST VERSUS LEVOCETIRIZINE IN THE TREATMENT OF SEASONAL RHINITIS AND CONJUNCTIVITIS IN CHILDREN 6-14 YEARS OLD | |||||||||||||
Medical condition: TREATMENT OF ALLERGIC SEASONAL RHINITIS AND ALLERGIC SEASONAL CONJUCTIVITIS | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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 |
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