- Trials with a EudraCT protocol (3)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3 result(s) found for: Hypoxic Ischaemic Encephalopathy.
Displaying page 1 of 1.
EudraCT Number: 2010-020797-41 | Sponsor Protocol Number: NEMO1-08NR26 | Start Date*: 2010-11-16 | |||||||||||
Sponsor Name:Only for Children Pharmaceuticals | |||||||||||||
Full Title: NEMO-1: An open label exploratory dose finding and pharmacokinetic clinical trial of bumetanide for the treatment of NEonatal seizure using Medication Off-patent. | |||||||||||||
Medical condition: Neonatal Seizures in Hypoxic Ischemic Encephalopathy | |||||||||||||
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Population Age: Newborns, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) FI (Prematurely Ended) GB (Prematurely Ended) SE (Prematurely Ended) FR (Ongoing) NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000770-29 | Sponsor Protocol Number: Ireland-RctV8 | Start Date*: 2018-06-18 | ||||||||||||||||
Sponsor Name:The Rotunda Hospital | ||||||||||||||||||
Full Title: Investigating the role of early low-dose aspirin in diabetes: A phase III multicentre double-blinded placebo-controlled randomised trial of low-dose aspirin initiated in the first trimester of diab... | ||||||||||||||||||
Medical condition: Pregestational type I or type II diabetes | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: IE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001119-38 | Sponsor Protocol Number: 116945 | Start Date*: 2015-09-21 | |||||||||||||||||||||
Sponsor Name:GlaxoSmithKline | |||||||||||||||||||||||
Full Title: A Phase IV, observer-blind, randomised, cross-over, placebo-controlled, multicentre study to assess the immunogenicity and safety of a single dose of Boostrix? in pregnant women. | |||||||||||||||||||||||
Medical condition: Booster immunisation against diphtheria, tetanus and pertussis diseases. The study population for this study will include pregnant women. | |||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||
Trial protocol: ES (Completed) CZ (Completed) FI (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
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