- Trials with a EudraCT protocol (36)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
36 result(s) found for: Crisis intervention.
Displaying page 1 of 2.
EudraCT Number: 2012-004892-37 | Sponsor Protocol Number: NL41205.018.12 | Start Date*: 2013-03-21 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: N-Acetylcysteine in patients with Sickle Cell Disease: Reducing the incidence of daily life pain in patients with sickle cell disease | |||||||||||||
Medical condition: Sickle Cell | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) BE (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003551-22 | Sponsor Protocol Number: 55029 | Start Date*: 2016-12-28 | ||||||||||||||||
Sponsor Name:Erasmus MC - Sophia Children's Hospital | ||||||||||||||||||
Full Title: STATIC IV: Efficacy of a loading dose of intravenous salbutamol in patients admitted to a PICU for severe acute asthma | ||||||||||||||||||
Medical condition: Severe acute (viral) wheeze and severe acute asthma | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000490-13 | Sponsor Protocol Number: EstuEla2022 | Start Date*: 2023-01-09 |
Sponsor Name:OILS4CURE S.L | ||
Full Title: Treatment, with a full spectrum extract of cannabis, in refractory epilepsy associated with tuberous sclerosis complex (TSC) | ||
Medical condition: Refractory epilepsy in tuberous sclerosis complex | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000563-14 | Sponsor Protocol Number: 2014-734 | Start Date*: 2015-07-22 | ||||||||||||||||||||||||||
Sponsor Name:Holbæk Sygehus, Region Sjælland i Danmark | ||||||||||||||||||||||||||||
Full Title: GDT in Urgent Abdominal Surgery - A Clinical Randomized Trial | ||||||||||||||||||||||||||||
Medical condition: Perforated intestinal diseases and obstructive bowel diseases with an urgent need for surgery. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-000897-21 | Sponsor Protocol Number: N01280 | Start Date*: 2008-02-05 | |||||||||||
Sponsor Name:UCB, Inc. | |||||||||||||
Full Title: A multi-center, double-blind, historical control, randomized conversion to monotherapy study with Keppra XR for treatment of partial onset seizures | |||||||||||||
Medical condition: partial onset seizures | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000469-18 | Sponsor Protocol Number: IP2018CS01 | Start Date*: 2020-06-26 |
Sponsor Name:Initiator Pharma | ||
Full Title: A Randomised, Double-Blind, Placebo-Controlled, Crossover Trial Studying the Efficacy and Safety of IP2018 in Depressed, Erectile Dysfunction (ED) Patients | ||
Medical condition: Male patients with a diagnosis of mild to moderate depression and ED as determined from the Hamilton depression scale score of 7 to 23 and International Index of Erectile Function (IIEF-5) score of... | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002787-32 | Sponsor Protocol Number: RG_19-172 | Start Date*: 2020-11-16 |
Sponsor Name:University of Birmingham | ||
Full Title: Antidepressant for the prevention of DEPression following first episode Psychosis trial | ||
Medical condition: Patients with First Episode Psychosis. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002195-40 | Sponsor Protocol Number: 13/0656 | Start Date*: 2014-09-02 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: A randomised controlled trial of the ketogenic diet in the treatment of epilepsy in children under the age of two years | |||||||||||||
Medical condition: Epilepsy | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
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: 2005-005122-31 | Sponsor Protocol Number: CL2-16257-060 | Start Date*: 2006-04-25 | |||||||||||
Sponsor Name:Institut de Recherches Internationales (for France) [...] | |||||||||||||
Full Title: Evaluation of the effects on heart rate, haemodynamic parameters, safety and tolerability of 5 mg bolus of ivabradine followed by 8-hour infusion at the dose of 5 mg of ivabradine given after a per... | |||||||||||||
Medical condition: Acute Myocardial Infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005578-24 | Sponsor Protocol Number: OPT-OMA-ASTHMA | Start Date*: 2022-03-10 | |||||||||||
Sponsor Name:Consorci Mar Parc de Salut de Barcelona (Parc de Salut MAR) | |||||||||||||
Full Title: Therapheutic optimization of omalizumab in allergic severe asthma patients by dose and frequency of administration adjustment | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004748-27 | Sponsor Protocol Number: EPIDAURUS-2020 | Start Date*: 2022-04-21 | |||||||||||
Sponsor Name:LMU University Hospital Munich | |||||||||||||
Full Title: Escalated single platelet inhibition for one month plus direct oral anticoagulation in patients with atrial fibrillation and acute coronary syndrome undergoing percutaneous coronary intervention | |||||||||||||
Medical condition: Patients with atrial fibrillation and ST-segment elevation myocardial infarction (STEMI) or non-ST-segment elevation myocardial infarction (NSTEMI) (biomarker -positive acute coronary syndrome) und... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010608-27 | Sponsor Protocol Number: ANG692 | Start Date*: 2009-11-20 | |||||||||||
Sponsor Name:MUMC+ | |||||||||||||
Full Title: A prospective cohort study to investigate the use of alfa V beta 3 integrin scintigraphic imaging with 99mTC-NC100692 to predict scar formation and heart failure after myocardial infarction in pati... | |||||||||||||
Medical condition: Myocardial infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002407-14 | Sponsor Protocol Number: 106915 | Start Date*: 2006-10-24 | |||||||||||
Sponsor Name:GlaxoSmithKline Research, European Medical Governance | |||||||||||||
Full Title: Eptifibatide Versus Abciximab in primary PCI for Acute ST elevation Myocardial Infarction (EVA-AMI) | |||||||||||||
Medical condition: Primary percutaneous coronary intervention (PCI) for ST-elevation Myocardial Infarction (STEMI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002931-95 | Sponsor Protocol Number: LCC2010.01 | Start Date*: 2008-01-30 | |||||||||||
Sponsor Name:UZ Leuven | |||||||||||||
Full Title: The Effects of Nitric Oxide for Inhalation on Myocardial Infarction Size. | |||||||||||||
Medical condition: Myocardial Infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Prematurely Ended) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003509-28 | Sponsor Protocol Number: UF 8042 | Start Date*: 2008-09-03 | |||||||||||
Sponsor Name:CHRU Montpellier - Direction de la Recherche, Partenariats et Réseaux, Relations avec l'Université | |||||||||||||
Full Title: Intérêt de l’administration intra-coronaire d’une dose unique d’EPO lors de la reperfusion chez des patients hospitalisés pour un primo infarctus avec sus-décalage persistant du segment ST | |||||||||||||
Medical condition: Patients hospitalisés pour un primo infarctus avec sus-décalage persistant du segment ST | |||||||||||||
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Population Age: Adults, Elderly | Gender: | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002709-36 | Sponsor Protocol Number: AK2017-3 | Start Date*: 2017-11-21 | ||||||||||||||||
Sponsor Name:Rigshospitalet, Department of Physiology, Nuclear Medicine and PET | ||||||||||||||||||
Full Title: Phase II: 68Ga-NODAGA-E[c(RGDyK)]2 Angiogenese PET for imaging angiogenesis in ST-Elevation Myocardial Infarction(STEMI) | ||||||||||||||||||
Medical condition: ST-Elevation Myocardial Infarction (STEMI) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-003903-23 | Sponsor Protocol Number: P150946J | Start Date*: 2018-03-02 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Assessment of Beta blocker interruption after uncomplicated mYocardial infarction on Safety and Symptomatic cardiac events requiring hospitalization: The ABYSS Study | |||||||||||||
Medical condition: Myocardial infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003703-16 | Sponsor Protocol Number: GR-2021-12375001 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | ||||||||||||||||||
Full Title: The effect of phoSPHocreatine on mEdical emergency team (met) tREated patients: a randomized clinical trial protocol - SPHERE. | ||||||||||||||||||
Medical condition: Patients with worsening clinical condition requiring MET intervention and in general ward | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006404-11 | Sponsor Protocol Number: PERFECT001(M-2006-144) | Start Date*: 2008-03-19 | |||||||||||
Sponsor Name:Miltenyi Biotec GmbH | |||||||||||||
Full Title: INTRAMYOCARDIAL TRANSPLANTATION OF BONE MARROW STEM CELLS FOR IMPROVEMENT OF POST-INFARCT MYOCARDIAL REGENERATION IN ADDITION TO CABG SURGERY: a controlled prospective, randomized, double blinded m... | |||||||||||||
Medical condition: Coronary artery disease after myocardial infarction with an indication for CABG surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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