- Trials with a EudraCT protocol (447)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5)
447 result(s) found for: Emergency care.
Displaying page 1 of 23.
EudraCT Number: 2015-002485-24 | Sponsor Protocol Number: CHUBX2014/09 | Start Date*: 2015-08-11 |
Sponsor Name:CHU de Bordeaux | ||
Full Title: Effectiveness of oral prednisolone versus partial endodontic treatment on pain reduction in emergency care of acute irreversible pulpitis of mandibular molars: study protocol for a non inferiority ... | ||
Medical condition: Pulpitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002686-15 | Sponsor Protocol Number: CHUBX2021/25 | Start Date*: 2022-10-18 |
Sponsor Name:CHU de Bordeaux | ||
Full Title: Effectiveness of an Optimisation Strategy for Emergency Tracheal Intubation on postintubation Morbidity: A cluster randomized controlled trial | ||
Medical condition: respiratory distress | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003220-36 | Sponsor Protocol Number: 45112 | Start Date*: 2014-05-21 |
Sponsor Name:Albert Schweitzer hospital | ||
Full Title: Remifentanil use for procedural sedation and analgesia in the emergency department | ||
Medical condition: The research will be conducted in patients that need short painfull treatment in the emergency department and with an indication for PSA. These treatments include: repositioning of fractures, repos... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001601-82 | Sponsor Protocol Number: MR311-3506(AMBU-001) | Start Date*: 2019-07-08 |
Sponsor Name:Mundipharma Pharmaceuticals B.V. | ||
Full Title: Open randomized clinical trial to compare pain relief between low-dose methoxyflurane and standard of care for the treatment of patients with trauma pain in emergency medical services in the Nether... | ||
Medical condition: Patients with moderate trauma pain due to extremity injuries for whom the emergency medical services have been called. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000194-31 | Sponsor Protocol Number: PenCTU/2010/CTIMP-004 | Start Date*: 2011-05-20 |
Sponsor Name:Plymouth Hospitals NHS Trust | ||
Full Title: An open randomised trial of patient controlled analgesia (PCA) versus routine care in the Emergency Department | ||
Medical condition: Patients presenting to the Emergency Department in severe pain from either musculoskeletal injury or non-traumatic abdominal pain. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-001665-16 | Sponsor Protocol Number: 1312 | Start Date*: 2013-08-01 |
Sponsor Name:University Hospital Grenoble | ||
Full Title: Intranasal Sufentanyl analgesia Versus Morphine IV in Emergency room. | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002498-80 | Sponsor Protocol Number: 06062019 | Start Date*: 2019-09-24 | |||||||||||
Sponsor Name:Mikkel Brabrand | |||||||||||||
Full Title: Will titrated oxygen flow to a peripheral oxygen saturation of 88-92% compared with oxygen flow to a saturation >94% reduce mortality in Chronic Obstructive Pulmonary Disease patients with acute ex... | |||||||||||||
Medical condition: Acute COPD Exacerbation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001081-80 | Sponsor Protocol Number: NL22172 | Start Date*: 2008-06-20 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Relevance of Biomarkers and Clinical Predictors of Outcome in Unselected Population with Febrile Urinary Tract Infection at Primary Care and Emergency Department in a Prospective, Randomized Cohort... | ||
Medical condition: To determine whether a 7-day duration of antibiotic treatment is non inferior to 14-day standard duration of treatment in adults presenting at primary care or emergency department with febrile uri... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004469-28 | Sponsor Protocol Number: MR311-4501 | Start Date*: 2018-03-01 | |||||||||||
Sponsor Name:MUNDIPHARMA | |||||||||||||
Full Title: Multicentre, randomised, double-blind study assessing the efficacy and safety of Penthrox® combined with a standard analgesia (SoC) in comparison to a placebo combined with a standard analgesia (So... | |||||||||||||
Medical condition: Emergency relief of moderate to severe pain associated with trauma in conscious adult patients | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001401-25 | Sponsor Protocol Number: QHD00012 | Start Date*: 2019-09-27 | |||||||||||
Sponsor Name:Sanofi Pasteur Inc. | |||||||||||||
Full Title: Relative Effectiveness of a High-Dose Quadrivalent Influenza Vaccine versus a Standard-Dose Quadrivalent Influenza Vaccine in Subjects 65 Years of Age and Older | |||||||||||||
Medical condition: Prevention of influenza infection in adults from 65 years of age and older | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000333-36 | Sponsor Protocol Number: 17012006 | Start Date*: 2006-04-26 |
Sponsor Name:Hull & East Yorkhire NHS Hospitals Trust | ||
Full Title: A randomised comparison of 0.5% levobupivacaine with a lidocaine/epinephrine/ fentanyl mixture for epidural top up for emergency caesarean section after “low dose” epidural for labour | ||
Medical condition: pregnant women, in labour requiring emergency caesarean section under epidural anaesthesia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-003145-42 | Sponsor Protocol Number: DEXAURP | Start Date*: 2014-02-26 | |||||||||||
Sponsor Name:FRANCISCO JAVIER BENITO FERNANDEZ | |||||||||||||
Full Title: PILOT RANDOMISED CONTROLLED TRIAL USIDNG DEXAMETHASONE VESUS PREDNISOLONA/PREDNISONA IN CHILDREN WITH ACUTE ASTHMA IN PEDIATRIC EMERGENCY WARD | |||||||||||||
Medical condition: ASTHMA | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001867-22 | Sponsor Protocol Number: PRETIC | Start Date*: 2018-09-27 | |||||||||||
Sponsor Name:Banc de Sang i teixits | |||||||||||||
Full Title: TRANSFUSION OF RED BLOOD CELLS, TRANEXAMIC ACID AND FIBRINOGEN CONCENTRATE FOR SEVERE TRAUMA HEMORRHAGE AT PRE-HOSPITAL PHASE OF CARE. A PILOT TRIAL. | |||||||||||||
Medical condition: TREATMENT OF SEVERE TRAUMA HEMORRHAGE AT PRE-HOSPITAL PHASE OF CARE. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (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: 2009-009596-35 | Sponsor Protocol Number: | Start Date*: 2009-03-17 |
Sponsor Name:Queen Mary's, University of London | ||
Full Title: Optimisation of Peri-operative Cardiovascular Management to Improve Surgical Outcome (Optimise Trial) | ||
Medical condition: Post-operative complications in patients who undergo major surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001889-10 | Sponsor Protocol Number: STOIC | Start Date*: 2020-06-02 |
Sponsor Name:University of Oxford, Clinical Trials and Research Governance | ||
Full Title: Use of inhaled corticosteroids as treatment of early COVID-19 infection to prevent clinical deterioration and hospitalisation | ||
Medical condition: COVID 19 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2021-000890-10 | Sponsor Protocol Number: MP0420-CP302 | Start Date*: 2021-05-03 | |||||||||||
Sponsor Name:Molecular Partners AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multicenter study of ensovibep (MP0420) in ambulatory adult patients with symptomatic COVID-19 | |||||||||||||
Medical condition: Symptomatic COVID-19 in ambulatory patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005395-40 | Sponsor Protocol Number: NSAP-01 | Start Date*: 2007-05-03 | |||||||||||
Sponsor Name:Barts and The London NHS Trust | |||||||||||||
Full Title: Is Buscopan, paracetamol or a combination of both the most effective analgesia for the treatment of non-specific abdominal pain? | |||||||||||||
Medical condition: Adult subjects attending the emergency department complaining of acute abdominal pain | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022001-18 | Sponsor Protocol Number: RESP_301_2010 | Start Date*: 2011-06-30 | ||||||||||||||||
Sponsor Name:University College Dublin Clinical Research Centre | ||||||||||||||||||
Full Title: A Randomised Trial of Single Dose Oral Dexamethasone versus Multi-Dose Prednisolone in the Treatment of Acute Exacerbations of Asthma in children who attend the Emergency Department | ||||||||||||||||||
Medical condition: Exacerbation of asthma in children presenting to the Emergency Department | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: IE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000224-35 | Sponsor Protocol Number: RECEM00001 | Start Date*: 2021-07-28 | |||||||||||
Sponsor Name:Marie Kristine Jessen | |||||||||||||
Full Title: Restrictive Fluid Administration vs. Standard of Care in Emergency Department Sepsis Patients - a Multicenter, Randomized Clinical Feasibility Trial | |||||||||||||
Medical condition: Sepsis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
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