- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (14)
7 result(s) found for: Croup.
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EudraCT Number: 2009-014376-22 | Sponsor Protocol Number: MC/PR/1404/003/09 | Start Date*: 2010-02-15 | |||||||||||
Sponsor Name:CHIESI | |||||||||||||
Full Title: MULTICENTRE, RANDOMIZED, DOUBLE-BLIND, PLACEBOCONTROLLED, TWO-ARM PARALLEL GROUPS STUDY DESIGN TO DEMONSTRATE THE EFFICACY AND TOLERABILITY OF A SINGLE DOSE OF BDP SUSPENSION FOR NEBULISATION 16... | |||||||||||||
Medical condition: CROUP (acute laryngotracheobronchitis) | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001611-30 | Sponsor Protocol Number: AJAE1001 | Start Date*: 2006-08-22 |
Sponsor Name:Hammersmith Hospital NHS Trust | ||
Full Title: Clinical trial comparing the effect of Acetaminophen and Ibuprofen on the duration of influenza viral shedding in young children (Pilot study) | ||
Medical condition: Influenza in children [positive rapid diagnostic test (QuickVue influenza test)confirmed by influenza PCR] Infants and young children shed the influenza virus for longer periods than adults, durat... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2017-000220-10 | Sponsor Protocol Number: ICON-CA209-9FN | Start Date*: 2017-10-31 | |||||||||||
Sponsor Name:Oslo University Hospital | |||||||||||||
Full Title: A randomized phase IIb study evaluating immunogenic chemotherapy combined with ipilimumab and nivolumab in patients with luminal B breast cancer | |||||||||||||
Medical condition: Metastatic hormone receptor positive breast cancer (primary or recurrent), defined as ER+ >1% in metastatic biopsy (archival material or study biopsy) and HER2 negative in the last biopsy evaluable... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005740-83 | Sponsor Protocol Number: 4825 | Start Date*: 2007-01-12 | |||||||||||
Sponsor Name:University of Southampton | |||||||||||||
Full Title: A Pragmatic Randomised Trial of Ibuprofen, Paracetamol, Steam and Delayed Prescribing for Patients with Respiratory Tract Infections in Primary Care | |||||||||||||
Medical condition: Inclusion criteria Patients aged 3 to 65 presenting to a GP or nurse with an RTI (acute cold, influenza, sore throat, otitis media, sinusitis, croup, or lower respiratory tract infection). Exclus... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001514-97 | Sponsor Protocol Number: 114541 | Start Date*: 2015-05-27 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A Phase 3, observer blind, randomized, non-influenza vaccine comparator-controlled, multi-country and multi-centre study of the efficacy of GSK Biologicals’ quadrivalent, inactivated, split virion,... | ||
Medical condition: Healthy volunteers (Immunization against influenza in male and female subjects 3 to 8 years of age inclusive) | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2011-001696-39 | Sponsor Protocol Number: AKF 379 | Start Date*: 2011-07-06 | |||||||||||
Sponsor Name:University of Southern Denmark, Clinical Pharmacology | |||||||||||||
Full Title: The inhibitory effect of metformin on gluconeogenesis in relation to polymorphisms in Organic Cation Transporter 1 (OCT1) in healthy volunteers | |||||||||||||
Medical condition: Healthy volunteers (diabetes mellitus 2) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003579-16 | Sponsor Protocol Number: BIOMIN | Start Date*: 2021-04-07 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:BIOMIN, a. s. | |||||||||||||||||||||||||||||||||||||||||||
Full Title: Multicenter, randomized, 52-week trial to determine the efficacy, adherence, safety, and tolerability of natural calcium and vitamin D3 and vitamin K2 supplementation, respectively, in postmenopaus... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Osteopenia | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: SK (Completed) CZ (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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