- Trials with a EudraCT protocol (99)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
99 result(s) found for: Bronchial challenge test.
Displaying page 1 of 5.
EudraCT Number: 2010-023945-31 | Sponsor Protocol Number: PRINA | Start Date*: 2010-12-17 |
Sponsor Name:AZIENDA OSPEDALIERA S. PAOLO (A.O. DI RILIEVO NAZIONALE) | ||
Full Title: Effect of Prasugrel sull'iperreattivita' bronchial and markers of airway inflammation in patients with chronic asthma: randomized crossover pilot study (Study PRINA). | ||
Medical condition: bronchial asthma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005838-12 | Sponsor Protocol Number: OC000459/004/05 | Start Date*: 2006-03-30 | |||||||||||
Sponsor Name:Oxagen Ltd | |||||||||||||
Full Title: A PHASE II STUDY OF THE EFFICACY (AS ASSESSED BY BRONCHIAL ALLERGEN CHALLENGE) AND SAFETY OF OC000459 DOSED ORALLY (200mg BID WITH FOOD) IN SUBJECTS WITH ALLERGIC ASTHMA; IN A RANDOMISED, DOUBLE BL... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001483-29 | Sponsor Protocol Number: CCD-1202-PR-0080 | Start Date*: 2012-08-08 | |||||||||||
Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
Full Title: A RANDOMISED, DOUBLE-BLIND, PLACEBO-CONTROLLED, THREE-WAY CROSSOVER STUDY TO EVALUATE THE EFFICACY AFTER ALLERGEN CHALLENGE, SAFETY, AND TOLERABILITY OF TWO DOSES OF INHALED CHF6001 DPI AFTER 9 DAY... | |||||||||||||
Medical condition: asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004345-14 | Sponsor Protocol Number: FB/PS/14/169/07 | Start Date*: 2007-12-05 | |||||||||||
Sponsor Name:Chiesi Farmaceutici SpA | |||||||||||||
Full Title: Dose response evaluation of CHF 1535 HFA pMDI in asthmatic patients using lung function, adenosine monophosphate bronchial challenge and fractional exhaled nitric oxide (FENO). Randomized, double... | |||||||||||||
Medical condition: Mild Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-009556-21 | Sponsor Protocol Number: KUH5801112 | Start Date*: 2009-03-30 | |||||||||||
Sponsor Name:Heikki Koskela | |||||||||||||
Full Title: Saline challenge in monitoring asthma control | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000939-86 | Sponsor Protocol Number: FLT4501 | Start Date*: 2011-06-16 | |||||||||||
Sponsor Name:Mundipharma AB | |||||||||||||
Full Title: An open-label single site single dose pilotstudy using mannitol challenge test with the purpose to explore treatment with fixed dose combinations in adult subjects with asthma in primary care in Sw... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016592-29 | Sponsor Protocol Number: SHO001 | Start Date*: 2010-03-05 | |||||||||||
Sponsor Name:University of Dundee | |||||||||||||
Full Title: Reversibility of Acute β-Blocker Induced Bronchoconstriction | |||||||||||||
Medical condition: asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001729-28 | Sponsor Protocol Number: IPI-145-03 | Start Date*: 2012-07-17 | |||||||||||
Sponsor Name: Infinity Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multi-Dose, Cross-Over, Efficacy and Safety Study of IPI-145 in Mild Asthmatic Subjects Undergoing Allergen Challenge | |||||||||||||
Medical condition: Mild asthma with allergen challenge | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000120-28 | Sponsor Protocol Number: RSPR-007 | Start Date*: 2015-03-19 | |||||||||||
Sponsor Name:RSPR Pharma AB | |||||||||||||
Full Title: A Double-Blind, Randomised, Placebo-controlled, Cross-over, Phase 2 Mannitol Challenge Study, Investigating the Efficacy of CRD007 in Adult Subjects with Asthma | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004102-13 | Sponsor Protocol Number: AcadMed CTU210406 | Start Date*: 2006-10-16 | |||||||||||
Sponsor Name:Hull and east yorkshire Hospitals Trust | |||||||||||||
Full Title: An 8 week, non-selected, cohort, study to investigate whether the treatment of reflux induced cough alters associated bronchial hyperresponsiveness. | |||||||||||||
Medical condition: Bronchial hyper-responsiveness in relation to reflux associated chronic cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016904-21 | Sponsor Protocol Number: SD-MLK | Start Date*: 2010-04-22 | |||||||||||||||||||||
Sponsor Name:Medisch Spectrum Twente | |||||||||||||||||||||||
Full Title: The predictive value of the acute effect of montelukast on an exercise challenge test for the outcome of longterm treatment with montelukast | |||||||||||||||||||||||
Medical condition: Exercise induced asthma / bronchoconstriction Asthma | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-009873-87 | Sponsor Protocol Number: FLT2503 | Start Date*: 2009-09-08 | |||||||||||
Sponsor Name:Mundipharma Research Ltd. | |||||||||||||
Full Title: A double-blind, randomised, incomplete block, crossover, placebo-controlled, dose-response study to assess bronchial hyperresponsiveness and airway inflammation effects of FlutiForm® pMDI low and h... | |||||||||||||
Medical condition: Asthma bronchial | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002477-22 | Sponsor Protocol Number: R1908-1909-ALG-1703 | Start Date*: 2019-01-25 | ||||||||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A PHASE 2, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY IN CAT-ALLERGIC PATIENTS WITH ASTHMA TO EVALUATE THE EFFICACY OF A SINGLE DOSE OF REGN1908-1909 TO REDUCE BRONCHOCONSTR... | ||||||||||||||||||
Medical condition: Cat-allergic asthma and Bronchoconstriction Upon Cat Allergen Challenge | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-002276-27 | Sponsor Protocol Number: PVSD-ICS | Start Date*: 2016-08-04 | |||||||||||
Sponsor Name:Medisch Spectrum Twente | |||||||||||||
Full Title: The predictive value of the acute effect of beclomethasone-dipropionate on a mannitol challenge test for the outcome of longterm treatment with beclomethasone-dipropionate in childhood asthma | |||||||||||||
Medical condition: exercise induced bronchoconstriction asthma | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001858-70 | Sponsor Protocol Number: AGO/2007/002 | Start Date*: 2007-11-15 | |||||||||||
Sponsor Name:University Hospital Ghent | |||||||||||||
Full Title: Effect of inhaled tiotropium bromide on neurokinin-A induced bronchoconstriction in asthma. | |||||||||||||
Medical condition: mild asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003795-35 | Sponsor Protocol Number: Griac001 | Start Date*: 2006-10-03 | |||||||||||
Sponsor Name:University Medical Center Groningen | |||||||||||||
Full Title: Mannitol inhalations as a faster procedure for testing of airways hyperresponsiveness | |||||||||||||
Medical condition: Detection of airway hyperresponsiveness in patients with asthma or COPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004152-71 | Sponsor Protocol Number: ICA 17043-17 | Start Date*: 2008-09-05 | |||||||||||
Sponsor Name:Icagen, Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo Controlled, Parallel-Group, Multicenter Study to Assess the Safety and Efficacy of TWO Weeks of Oral Senicapoc Administration on Allergen challenge in ... | |||||||||||||
Medical condition: Asthma. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002512-89 | Sponsor Protocol Number: ANDA1 | Start Date*: 2012-01-26 | |||||||||||
Sponsor Name:Tayside Clinical Trials Unit, University of Dundee | |||||||||||||
Full Title: Evaluation of any steroid sparing effect of beta blocker therapy on airway hyper-responsiveness in stable, mild to moderate, asthmatics. | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006576-11 | Sponsor Protocol Number: 31318 | Start Date*: 2008-06-13 | |||||||||||
Sponsor Name:Nottingham University | |||||||||||||
Full Title: Macrolides in Refractory Asthma | |||||||||||||
Medical condition: Refractory asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012675-10 | Sponsor Protocol Number: D4050169 | Start Date*: 2009-10-01 | ||||||||||||||||
Sponsor Name:Dainippon Sumitomo Pharma Europe Ltd. | ||||||||||||||||||
Full Title: An exploratory, randomised, double blind, placebo controlled, 14 day, two-way crossover, inhaled allergen challenge study to evaluate the effects of SMP-028 in subjects with mild to moderate asthma | ||||||||||||||||||
Medical condition: Asthma and Allergic Rhinitis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
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