- Trials with a EudraCT protocol (31)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
31 result(s) found for: Childhood Asthma AND Asthma.
Displaying page 1 of 2.
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: 2011-001643-79 | Sponsor Protocol Number: SAS115358 | Start Date*: 2012-01-24 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A 6-month safety and benefit study of inhaled fluticasone propionate/ salmeterol combination versus inhaled fluticasone propionate in the treatment of 6,200 pediatric subjects 4-11 years old with p... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (Completed) LV (Completed) CZ (Completed) LT (Completed) ES (Completed) AT (Completed) SE (Not Authorised) BE (Completed) DK (Completed) NL (Completed) BG (Completed) IT (Completed) FI (Prematurely Ended) SK (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004420-42 | Sponsor Protocol Number: COPSACazt | Start Date*: 2022-01-12 | ||||||||||||||||
Sponsor Name:Herlev and Gentofte Hospital, Copenhagen Prospective Studies on Asthma in Childhood (COPSAC) | ||||||||||||||||||
Full Title: Azithromycin for treatment of hospitalized children with asthmatic symptoms - A double-blind, randomized, controlled study | ||||||||||||||||||
Medical condition: Childhood Asthma | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005678-76 | Sponsor Protocol Number: AIFANumberFARM94793N | Start Date*: 2013-08-30 | |||||||||||
Sponsor Name:ALLEGRIA onlus | |||||||||||||
Full Title: Twenty-four month, multicenter, prospective, randomized, double-blind, placebo controlled, parallel-group study to evaluate the efficacy, safety, tolerability, and cost-effectiveness of allergen sp... | |||||||||||||
Medical condition: Allergic asthma to house dust mites | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002337-20 | Sponsor Protocol Number: 2412325-2 | Start Date*: 2006-09-06 | |||||||||||
Sponsor Name:Erasmus Medical Centre Rotterdam | |||||||||||||
Full Title: Efficacy of peripherally targeted inhaled rhDNase for persistent obstructive asthma in childhood | |||||||||||||
Medical condition: Asthma is a chronic inflammatory disorder in which many cells play a role, in particular mast cells, eosinophils and T lymphocytes. In susceptible individuals this inflammation causes recurrent epi... | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000753-31 | Sponsor Protocol Number: HZA102942 | Start Date*: 2012-03-08 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, two-way crossover 14-day study to invstigate the safety, tolerability,pharmacodynamics and pharmacokinetics of repeat dose inhaled fluticasone furoa... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000741-12 | Sponsor Protocol Number: HZA112776 | Start Date*: 2012-03-08 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A Randomized, Double blind, Placebo controlled, Two-Way Crossover 7-day study to Investigate the Safety, Tolerability, Pharmacodynamics and Pharmacokinetics of Repeat Dose Inhaled GW642444 25μg in ... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004424-29 | Sponsor Protocol Number: 6727 | Start Date*: 2018-03-23 |
Sponsor Name:Academic Medical Center | ||
Full Title: Pharmacogenetics Use For Further treatment Improvement in childreN (PUFFIN) trial | ||
Medical condition: Children with persistent uncontrolled asthma | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000754-55 | Sponsor Protocol Number: HZA112777 | Start Date*: 2014-08-06 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A randomized, double-blind, repeat dose, two period crossover study to evaluate the safety and tolerability, pharmacokinetics, and pharmacodynamics of inhaled fluticasone furoate/vilanterol 100/2... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022458-18 | Sponsor Protocol Number: 205.425 | Start Date*: 2011-05-23 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: A phase II randomised, double-blind, placebo-controlled incomplete cross-over trial with 4-week treatment periods to evaluate efficacy and safety of tiotropium inhalation solution (doses of 1.25 μg... | |||||||||||||
Medical condition: Moderate persistent asthma in children 6 to 11 years old | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LV (Completed) LT (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003404-14 | Sponsor Protocol Number: BUSAL-SD201 | Start Date*: 2021-01-27 | |||||||||||
Sponsor Name:Laboratoires SMB S.A. | |||||||||||||
Full Title: A comparative study to assess a fixed-dose combination of Budesonide-Salmeterol versus Serevent® Diskus® 50 μg + Pulmicort® Turbuhaler® 100 µg co-administrated in asthmatic children: single dose, c... | |||||||||||||
Medical condition: Regular treatment of asthma | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001559-37 | Sponsor Protocol Number: asthmavit1 | Start Date*: 2006-06-05 |
Sponsor Name:University of Aberdeen | ||
Full Title: A study to observe the effects of one month’s supplementation with forceval junior on asthma control in children aged 7-12 years with asthma. | ||
Medical condition: Asthma | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004085-17 | Sponsor Protocol Number: 19IC5548 | Start Date*: 2020-03-18 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: Treating severe paediatric asthma; a randomised controlled trial of mepolizumab and omalizumab (TREAT trial) | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003835-39 | Sponsor Protocol Number: FSS-AS-30003 | Start Date*: 2017-03-30 | |||||||||||
Sponsor Name:Teva Branded Pharmaceutical Products R&D, Inc. | |||||||||||||
Full Title: A 12-Week, Randomized, Double-Blind, Placebo-Controlled, Efficacy and Safety Study of Fluticasone Propionate Multidose Dry Powder Inhaler Compared with Fluticasone Propionate/Salmeterol Multidose D... | |||||||||||||
Medical condition: Persistent asthma | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
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: 2017-003330-91 | Sponsor Protocol Number: BUSAL-II-17-1 | Start Date*: 2017-11-29 | |||||||||||
Sponsor Name:Laboratoires SMB S.A. | |||||||||||||
Full Title: A pharmacokinetic and pharmacodynamic, randomised, single dose, cross-over, partially blinded study to compare the systemic exposure and the efficacy of a fixed-dose combination of Budesonide-Salme... | |||||||||||||
Medical condition: Regular Treatment of Asthma | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BG (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: 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: 2005-004115-29 | Sponsor Protocol Number: 25.08.2005 | Start Date*: 2006-03-17 |
Sponsor Name:Research Institute for the prevention of allergy and airway diseases in childhood | ||
Full Title: Investigation to identify predictors of response to a treatment with montelukast | ||
Medical condition: asthma bronchiale in childhood | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000907-41 | Sponsor Protocol Number: DM/PR/3301/003/05 | Start Date*: 2006-06-13 | |||||||||||
Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
Full Title: A single dose, randomised, double blind, double dummy, placebo-controlled, three-period crossover clinical study, comparing the efficacy, safety and tolerability of Formoterol-HFA pMDI 12 microgram... | |||||||||||||
Medical condition: Persistent moderate to severe childhood asthma (5 to 12 years of age, inclusive) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
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