- Trials with a EudraCT protocol (54)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (10)
54 result(s) found for: Acute severe asthma.
Displaying page 1 of 3.
EudraCT Number: 2007-006227-12 | Sponsor Protocol Number: SPON408-07 | Start Date*: 2008-03-18 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: A randomised, placebo controlled study of nebulised magnesium in acute severe asthma in children | |||||||||||||
Medical condition: Acute severe asthma | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004149-27 | Sponsor Protocol Number: I13106870 | Start Date*: 2009-01-06 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
Full Title: A Multi-Centre, Randomized, Double-Blind, Placebo-Controlled, Repeat-Dose study to evaluate the Efficacy and Safety of Intravenous GSK679586 in Patients with Severe Asthma | |||||||||||||
Medical condition: Severe asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) FR (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001644-29 | Sponsor Protocol Number: SAS115359 | Start Date*: 2012-05-04 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: SAS115359, a Safety and Efficacy Study of Inhaled Fluticasone Propionate/Salmeterol Combination versus Inhaled Fluticasone Propionate in the Treatment of Adolescent and Adult Subjects with Asthma. | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) AT (Completed) DE (Completed) ES (Completed) LT (Completed) SE (Completed) LV (Completed) HU (Completed) CZ (Completed) BE (Completed) NL (Completed) PL (Completed) IT (Completed) DK (Completed) SK (Completed) FI (Prematurely Ended) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004089-15 | Sponsor Protocol Number: AGO/2008/009 | Start Date*: 2008-09-11 |
Sponsor Name:University Hospital Ghent | ||
Full Title: The AZISAST Randomized Controlled Clinical Trial: Azithromycine as add-on therapy in Severe, Non-Eosinophilic Asthma | ||
Medical condition: Uncontrolled severe asthma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-007844-33 | Sponsor Protocol Number: CAT-354-MI-CP199 | Start Date*: 2009-04-06 | |||||||||||
Sponsor Name:MedImmune Limited | |||||||||||||
Full Title: A Phase 2a, Randomized, Double-blind, Placebo-controlled, Parallel-arm, Multicenter Study to Evaluate the Efficacy and Safety of CAT-354, a Fully Human Monoclonal Antibody Directed Against Interleu... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000190-81 | Sponsor Protocol Number: TIPP | Start Date*: 2021-12-29 |
Sponsor Name:Goethe-University Frankfurt | ||
Full Title: A prospective multicenter placebo-controlled trial to study the efficacy and safety of Tiotropium in preventing severe asthma exacerbations in partial and uncontrolled preschool asthma. TIPP-Study | ||
Medical condition: Severe asthma exacerbations in partial and uncontrolled preschool asthma | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Temporarily Halted) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000900-41 | Sponsor Protocol Number: WB28850 | Start Date*: 2013-05-10 |
Sponsor Name:F. Hoffmann-La Roche, Ltd. | ||
Full Title: A STUDY TO MEASURE SERUM PERIOSTIN, ASTHMA-RELATED BIOMARKERS AND RESPONSE TO PREDNISOLONE IN ADULT AND ADOLESCENT PATIENTS WITH SEVERE ORAL CORTICOSTEROID-DEPENDENT ASTHMA | ||
Medical condition: Severe corticosteroid-dependent asthma | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-002677-29 | Sponsor Protocol Number: 4739 | Start Date*: 2023-01-11 | ||||||||||||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA DI FERRARA | ||||||||||||||||||||||||||||
Full Title: Correlating Inflammatory Values of FEno, SymToms, SpuTum and Lung Function in Asthma | ||||||||||||||||||||||||||||
Medical condition: Asthma, a chronic inflammatory disease of the airways, is characterized by a variability of symptoms that can evolve in an acute and sometimes severe form. Treatment of asthma involves daily treatm... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003673-10 | Sponsor Protocol Number: AV003 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Bond Avillion 2 Development LP | ||||||||||||||||||
Full Title: A Long-term, Randomized, Double-blind, Multicenter, Parallel-group, Phase III Study Evaluating the Efficacy and Safety of PT027 Compared to PT007 Administered as Needed in Response to Symptoms in S... | ||||||||||||||||||
Medical condition: Moderate to severe asthma | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) CZ (Completed) GB (GB - no longer in EU/EEA) SK (Completed) ES (Completed) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003551-22 | Sponsor Protocol Number: 55029 | Start Date*: 2016-12-28 | ||||||||||||||||
Sponsor Name:Erasmus MC - Sophia Children's Hospital | ||||||||||||||||||
Full Title: STATIC IV: Efficacy of a loading dose of intravenous salbutamol in patients admitted to a PICU for severe acute asthma | ||||||||||||||||||
Medical condition: Severe acute (viral) wheeze and severe acute asthma | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002996-27 | Sponsor Protocol Number: 13CC34 | Start Date*: 2015-02-02 |
Sponsor Name:Great Ormond Street Hospital For Children NHS Foundation Trust | ||
Full Title: Optimising effectiveness and minimising toxicity of intravenous salbutamol in children with acute asthma | ||
Medical condition: The mainstay of asthma treatment worldwide are β2-agonists and steroids. Current management of childhood acute asthma is based on British Thoracic Society guidelines, which recommend IVS as second ... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-005553-31 | Sponsor Protocol Number: HZA115150 | Start Date*: 2012-06-18 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A 12-month, open label, randomised, effectiveness study to evaluate fluticasone furoate (FF, GW685698)/vilanterol (VI, GW642444) Inhalation Powder delivered once daily via a Novel Dry Powder Inhale... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023112-14 | Sponsor Protocol Number: 205.442 | Start Date*: 2011-03-24 | |||||||||||
Sponsor Name:Boehringer Ingelheim RCV GmbH & CoKG | |||||||||||||
Full Title: A Phase III, randomised, double-blind, placebo-controlled, parallel-group trial to evaluate efficacy and safety of tiotropium inhalation solution delivered via Respimat® inhaler (2.5 µg and 5 µg o... | |||||||||||||
Medical condition: Mild Persistent Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) HU (Completed) EE (Completed) SK (Completed) AT (Completed) IT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004959-50 | Sponsor Protocol Number: Heliox-AP | Start Date*: 2016-05-29 | |||||||||||
Sponsor Name:S.E. Carburos Metálicos S.A. grupo Air Products | |||||||||||||
Full Title: HELIOX-DRIVEN BETA2-AGONISTS NEBULIZATION FOR CHILDREN WITH MODERATE TO SEVERE ACUTE ASTHMA: A RANDOMIZED CONTROLLED TRIAL | |||||||||||||
Medical condition: Moderate to severe exacerbations of asthma | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001304-37 | Sponsor Protocol Number: 205715 | Start Date*: 2016-11-09 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A Phase III, randomized, double-blind, active controlled, parallel group study, comparing the efficacy, safety and tolerability of the fixed dose combination FF/UMEC/VI with the fixed dose dual co... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) ES (Completed) PL (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-003825-29 | Sponsor Protocol Number: 04/aaa1234. | Start Date*: 2005-06-06 |
Sponsor Name:Cardiff and Vale NHS Trust | ||
Full Title: MAGNET - a randomised placebo controlled trial of the use of nebulised magnesium sulphate in moderate/severe acute asthma in childhood | ||
Medical condition: MAGNET is a randomised placebo(isotonic saline) controlled trial of the use of nebulised magnesium sulphate in moderate/severe acute asthma in childhood. All children (2-16 years of age) presenting... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2010-018592-16 | Sponsor Protocol Number: Antibiotika | Start Date*: 2010-10-15 | |||||||||||
Sponsor Name:COPSAC | |||||||||||||
Full Title: Antibiotics as a treatment of repeated asthmatic symptoms in children. A randomized, controlled study within the ABC-cohort (Asthma Begins in Childhood) | |||||||||||||
Medical condition: Acute asthma exacerbations in children. | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001187-78 | Sponsor Protocol Number: 112897 | Start Date*: 2008-01-02 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: The 3Mg Trial: A randomised controlled trial of intravenous or nebulised magnesium sulphate versus standard therapy for acute severe asthma | |||||||||||||
Medical condition: Acute severe asthma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004158-10 | Sponsor Protocol Number: ALMED-07-C2-012 | Start Date*: 2008-04-17 |
Sponsor Name:AIR LIQUIDE | ||
Full Title: A single site, exploratory, phase I / II, randomised trial comparing the effect of Helium/Oxygen mixtures (He/O2 78:22 and He/O2 65:35) to medical air on pulmonary function in moderate / severe ast... | ||
Medical condition: - healthy volunteers, - moderate and severe persistent asthmatic patients, - moderate and severe COPD patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-002106-48 | Sponsor Protocol Number: BCF-2009.01 | Start Date*: 2012-07-06 |
Sponsor Name:University College Dublin | ||
Full Title: An Investigative Study to characterize gene expression patterns in myeloid cells that are triggered during acute asthma exacerbations, and to identify associated genes/gene networks that are Omaliz... | ||
Medical condition: Asthma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
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