- Trials with a EudraCT protocol (2,511)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,511 result(s) found for: Aged care.
Displaying page 1 of 126.
EudraCT Number: 2016-003582-25 | Sponsor Protocol Number: NL59128 | Start Date*: 2017-01-23 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: The added effect of oral ondansetron to care-as-usual on persisting vomiting in children aged 6 months to 6 years, presenting at primary care out of hours service with acute gastro-enteritis and co... | ||
Medical condition: Gastroenteritis | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005934-59 | Sponsor Protocol Number: DEXPEDICU | Start Date*: 2009-01-07 |
Sponsor Name:Kaija Puhakka | ||
Full Title: Pharmacokinetics of dexmedetomidine in paediatric intensive care patients | ||
Medical condition: Children aged 0 - 11 years admitted to paediatric intensive care unit and planned to be sedated and mechanically ventilated for at least 24 hours. The underlying medical conditions can be various k... | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001768-27 | Sponsor Protocol Number: P20/07 | Start Date*: 2020-04-27 | |||||||||||
Sponsor Name:CH Versailles | |||||||||||||
Full Title: "STUDY OF THE EFFICIENCY OF NORMAL HUMAN IMMUNOGLOBULINS (IVIG) IN PATIENTS AGED 75 YEARS AND OVER COVID-19 WITH SEVERE ACUTE RESPIRATORY FAILURE" GERONIMO 19 | |||||||||||||
Medical condition: Patients aged 75 years and older with confirmed infection Covid19 and saturation SaO2≤ under 95% O2> 5 L / min disqualified from a care in the ICU | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011051-51 | Sponsor Protocol Number: 112662 | Start Date*: 2009-07-27 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase III, double-blind, randomized study to demonstrate the non-inferiority of an aged lot of GlaxoSmithKline Biologicals' FLU NG vaccine in adults aged 65 years and above compared to a fresh lo... | ||
Medical condition: Immunization against influenza in male and female subjects aged greater than or equal to 65 years | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: EE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-000313-33 | Sponsor Protocol Number: NL72651 | Start Date*: 2020-07-08 |
Sponsor Name:UMC Utrecht | ||
Full Title: ‘Bronchodilators for wheeze in young children presenting to primary care: a randomised, placebo-controlled, multicentre, parallel group trial’ | ||
Medical condition: Wheezing in infants and young children (6-24 months old) | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) BE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2007-007645-12 | Sponsor Protocol Number: 250101 | Start Date*: 2008-07-15 |
Sponsor Name:University of York | ||
Full Title: The Randomised Evaluation of the Effectiveness and Acceptability of Computerised Therapy (REEACT) Trial | ||
Medical condition: Depression | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004621-40 | Sponsor Protocol Number: NL50760 | Start Date*: 2015-09-07 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: The effect of oral ondansetron on referral rate in children aged 6 months to 6 years attending in primary care out of hours service with acute gastro-enteritis and vomiting. | ||
Medical condition: Gastroenteritis | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001769-27 | Sponsor Protocol Number: CHI0465 | Start Date*: 2008-09-29 |
Sponsor Name:Southampton University Hospital Trust | ||
Full Title: Microbiological assessment of prophylactic ciprofloxacin therapy for children with cystic fibrosis during viral respiratory viral infection to prevent Pseudomonas aeruginosa colonisation – a random... | ||
Medical condition: Cystic Fibrosis Specifically the trial will include children aged 2-14 years with a diagnosis of cystic fibrosis and not chronically infected with pseudomonas aeruginosa in their lungs. | ||
Disease: | ||
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: 2017-000632-34 | Sponsor Protocol Number: AAUH-ICU-01 | Start Date*: 2017-04-25 | ||||||||||||||||
Sponsor Name:Department of Anaesthesia and Intensive Care Medicine, Aalborg University Hospital | ||||||||||||||||||
Full Title: Handling oxygenation targets in adults with acute hypoxaemic respiratory failure in the intensive care unit: A randomised clinical trial of a lower versus a higher oxygenation target Addendum: Tri... | ||||||||||||||||||
Medical condition: Acute hypoxaemic respiratory failure in patients admitted to the intensive care unit Addendum: Acute hypoxaemic respiratory failure in patients admitted to the intensive care unit with COVID-19 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000953-38 | Sponsor Protocol Number: MK-1986-014 | Start Date*: 2018-02-07 | |||||||||||
Sponsor Name:Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase 1, Single-and Multiple-Dose Safety and Pharmacokinetic Study of Oral and IV Tedizolid Phosphate (MK-1986) in Inpatients Under 2 Years Old | |||||||||||||
Medical condition: Treatment or prophylaxis against Gram-positive infections | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) GB (GB - no longer in EU/EEA) NO (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012188-32 | Sponsor Protocol Number: 113094 | Start Date*: 2009-09-17 |
Sponsor Name:GlaxosmithKline Biologicals | ||
Full Title: A phase III, observer-blind, multicountry, multicentre study to evaluate the safety, reactogenicity and immunogenicity of GlaxoSmithKline Biologicals’ GSK2186877A influenza vaccine administered to ... | ||
Medical condition: Immunization against influenza in male and female subjects aged 19-43 years and 66 years or older. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) SE (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000500-26 | Sponsor Protocol Number: 01-1-101 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Rapidscan Pharma Solutions EU Ltd (RPS EU Ltd) | |||||||||||||
Full Title: An Open-label, Single Ascending-dose, Pharmacokinetic and Safety Study of Regadenoson (Rapidscan®) in Paediatric Patients with Cardiovascular Conditions and Diseases | |||||||||||||
Medical condition: Regadenoson will be used as a pharmacologic stress agent in paediatric patients with cardiovascular problems, undergoing a clinically indicated myocardial perfusion MRI | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003339-22 | Sponsor Protocol Number: V70P2E1 | Start Date*: 2007-10-11 |
Sponsor Name:Novartis Vaccines and Diagnostics S.r.l. | ||
Full Title: A Phase II, Observer-Blind, Parallel Groups, Single-Center, Extension Study to Evaluate the Immunogenicity and Safety Following a Single Intramuscular Dose of FLUAD or Vaxigrip Influenza Vaccines i... | ||
Medical condition: Influenza | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-005409-26 | Sponsor Protocol Number: 20200708 | Start Date*: 2021-06-11 | |||||||||||
Sponsor Name:Copenhagen University Hospital, Rigshospitalet | |||||||||||||
Full Title: The PREVENT AGITATION trial II – children ≤1 year | |||||||||||||
Medical condition: Emergence agitation | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000576-33 | Sponsor Protocol Number: RBN 542 | Start Date*: 2006-06-13 |
Sponsor Name:St Helens & Knowsley Hospitals NHS Trust [...] | ||
Full Title: Pilot Study to investigate the role of Glutamine in the early protective stress response | ||
Medical condition: Critical Illness | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000197-53 | Sponsor Protocol Number: 2011-000197-53 | Start Date*: 2011-04-15 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: Effects of Potassium Sparing Diuretics on Potassium Urinary Output, Plasma Levels and Cardiac Arrhythmias in Neurocritical Care Patients Receiving Mannitol Therapy for Cerebral Edema: double blind,... | |||||||||||||
Medical condition: Acute Cerebral Edema | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002012-27 | Sponsor Protocol Number: KEDOB | Start Date*: 2013-10-30 |
Sponsor Name:LANDSTINGET I ÖSTERGÖTLAND | ||
Full Title: Ketamine dose finding study in pediatric burn wound care | ||
Medical condition: Pediatric burn patients who need rectal sedation during wound care | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001950-33 | Sponsor Protocol Number: 15/0592 | Start Date*: 2018-01-19 | |||||||||||
Sponsor Name:UCL | |||||||||||||
Full Title: Methylphenidate versus placebo for fatigue in advanced cancer (MePFAC) | |||||||||||||
Medical condition: Cancer-related fatigue | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003238-14 | Sponsor Protocol Number: 104888, 107509 | Start Date*: 2006-09-26 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase II/III, observer-blind, multicountry, multicentre, randomized study to demonstrate the superiority in terms of immunogenicity of AS25 adjuvanted influenza vaccine administered in adults age... | ||
Medical condition: Healthy subjects, Immunization against influenza in male and female subjects aged ≥ 50 years. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) NO (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004190-46 | Sponsor Protocol Number: D5136C00013 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Randomised, Double-Blind, Parallel-Group, Multicentre, Phase III Study to Evaluate the Effect of Ticagrelor versus Placebo in Reducing the Number of Vaso-Occlusive Crises in Paediatric Patients A... | |||||||||||||
Medical condition: Sickle Cell Disease | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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