- Trials with a EudraCT protocol (26)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
26 result(s) found for: Resuscitation AND Cardiac Arrest.
Displaying page 1 of 2.
EudraCT Number: 2006-006453-27 | Sponsor Protocol Number: CNMPEPO 001 | Start Date*: 2007-02-01 | |||||||||||
Sponsor Name:Zdravstveni dom dr. Adolfa Drolca Maribor | |||||||||||||
Full Title: The use of epoetin beta in cardiac arrest victims: the impact on survival and neurological outcome | |||||||||||||
Medical condition: The aim of our prospective, randomized, multicentered and controlled research is to determine the impact of erythropoietin on survival and neurological outcome of cardiac arrest victims. On the bas... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001074-26 | Sponsor Protocol Number: S-CPR2011 | Start Date*: 2011-11-17 | |||||||||||
Sponsor Name:Medizinische Universität Graz, Universitätsklinik für Innere Medizin | |||||||||||||
Full Title: Effect of High Dose Selenium on Inflammation and Neurological Outcome after Cardiac Arrest: A randomized, double blind placebo controlled phase 2a study | |||||||||||||
Medical condition: Cardiac Arrest with successful resuscitation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022679-71 | Sponsor Protocol Number: Xenon-MTH-Studie | Start Date*: 2011-01-07 | |||||||||||
Sponsor Name:Clinical Trials Center Aachen, University of Aachen | |||||||||||||
Full Title: Xenon and Therapeutical Hypothermia After Successful Cardiopulmonary Resuscitation | |||||||||||||
Medical condition: In this clinical trial will be checked, whether 2 hours ventilation with xenon has neuroprotetctive effect on the patients, which had out of hospital cardiac arrest and successful cardiopulmonary r... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004311-45 | Sponsor Protocol Number: 2013-PharmaCA-001 | Start Date*: 2014-03-25 | |||||||||||
Sponsor Name:Copenhagen University Hospital Rigshospitalet, Department of Cardiology B 2143 | |||||||||||||
Full Title: GLP-1 ANALOGS FOR NEUROPROTECTION AFTER OUT-OF-HOSPITAL CARDIAC ARREST, A RANDOMIZED CLINICAL TRIAL | |||||||||||||
Medical condition: We investigate the efficacy of commercially available GLP-1 analog for reducing post anoxic brain injury in patients who remain comatose after having been resuscitation from out of hospital cardiac... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004773-13 | Sponsor Protocol Number: 00001 | Start Date*: 2018-02-27 | |||||||||||
Sponsor Name:Research Center for Emergency Medicine Department of Clinical Medicine Aarhus University | |||||||||||||
Full Title: Vasopressin and Methylprednisolone for In-Hospital Cardiac Arrest – A Randomized, Double-Blind, Placebo-Controlled Trial | |||||||||||||
Medical condition: The study will include patients with in-hospital cardiac arrest (IHCA). The study will test whether treatment with methylprednisolone and vasopressin added to standard care will improve survival fo... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017499-26 | Sponsor Protocol Number: Heres | Start Date*: 2010-03-16 | ||||||||||||||||||||||||||
Sponsor Name:Academical Medical Center, University of Amsterdam | ||||||||||||||||||||||||||||
Full Title: The use of Helium after Resuscitation: a safety and feasibility study | ||||||||||||||||||||||||||||
Medical condition: Persistent coma after cardiac arrest. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003047-32 | Sponsor Protocol Number: IRFMN-7557 | Start Date*: 2021-01-21 | |||||||||||
Sponsor Name:IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI | |||||||||||||
Full Title: CardioPulmonary resuscitation with Argon (CPAr) trial | |||||||||||||
Medical condition: Cardiac Arrest | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005922-82 | Sponsor Protocol Number: IVIO1.3 | Start Date*: 2022-01-13 | |||||||||||
Sponsor Name:Prehospital Emergency Medical Services, Central Denmark Region | |||||||||||||
Full Title: Intravenous vs. Intraosseous Vascular Access During Out-of-Hospital Cardiac Arrest - A Randomized Clinical Trial | |||||||||||||
Medical condition: Out-of-hospital cardiac arrest (OHCA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005178-30 | Sponsor Protocol Number: LRS-01-07-02 | Start Date*: 2008-01-09 | |||||||||||||||||||||
Sponsor Name:Life Recovery Systems | |||||||||||||||||||||||
Full Title: Clinical Study of the LRS ThermoSuit™ System in Post Arrest Patients with Intravenous Infusion of Magnesium Sulfate | |||||||||||||||||||||||
Medical condition: Post resusucitation disease after resuscitation from cardiac arrest | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000005-23 | Sponsor Protocol Number: Ghreline | Start Date*: 2018-12-12 |
Sponsor Name:University of Twente | ||
Full Title: Ghrelin treatment of comatose patients after cardiac arrest: A clinical trial to promote cerebral recovery | ||
Medical condition: Brain damage after cardiac arrest | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003265-26 | Sponsor Protocol Number: 345 | Start Date*: 2017-01-03 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Pharmacokinetic/Pharmacodynamic effects of add-on antiplatelet therapy with parenteral cangrelor as compared to standard dual antiplatelet treatment in patients with ST-elevation myocardial infarct... | ||
Medical condition: ST-elevation myocardial infarction, cardiac arrest | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2019-003387-46 | Sponsor Protocol Number: COCA2 | Start Date*: 2019-10-28 | |||||||||||
Sponsor Name:Research Center for Emergency Medicine Department of Clinical Medicine Aarhus University | |||||||||||||
Full Title: Calcium for Out-of-Hospital Cardiac Arrest – A Randomized, Double-Blind, Placebo-Controlled trial | |||||||||||||
Medical condition: The study will include patients with out-of-hospital cardiac arrest (OHCA). The study will test whether treatment with Calcium Chloride added to standard care will improve survival following OHCA. ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005876-21 | Sponsor Protocol Number: DANOHCA-001 | Start Date*: 2022-07-08 | |||||||||||
Sponsor Name:Department of Cardiology, Copenhagen University Hospital, Rigshospitalet | |||||||||||||
Full Title: The Danish Out-of-Hospital Cardiac Arrest study (DANOHCA) | |||||||||||||
Medical condition: We will investigate the efficacy of four interventions (two pharmaceutical) for reducing mortality and organ damage in patients resuscitated after out-of-hospital cardiac arrest. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001620-33 | Sponsor Protocol Number: APHP200033 | Start Date*: 2021-01-13 |
Sponsor Name:ASSISTANCE-PUBLIQUE HOPITAUX DE PARIS (AP-HP) | ||
Full Title: HYdrocortisone and VAsopressin in Post-RESuscitation Syndrome | ||
Medical condition: Adult cardiac arrest patients with sustained ROSC and hemodynamic failure due to post-resuscitation syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002226-22 | Sponsor Protocol Number: 2.0 | Start Date*: 2019-04-30 |
Sponsor Name:Medical University of Vienna | ||
Full Title: The Impact of Target Temperature Management on Drug Metabolism | ||
Medical condition: Patients after successful cardiopulmonary resuscitation who undergo target temperature management for 24h hours | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004318-25 | Sponsor Protocol Number: NL63681.029.18 | Start Date*: 2019-04-16 | |||||||||||
Sponsor Name:VU University Medical Center | |||||||||||||
Full Title: Early high-dose vitamin C in post-cardiac arrest syndrome. | |||||||||||||
Medical condition: Patients admitted to the Intensive Care after out-of-hospital cardiac arrest with return of spontaneous circulation, ventricular fibrillation or ventricular tachycardia as first registered cardiac ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003595-11 | Sponsor Protocol Number: 2004-06-DP-119-RKF-25 | Start Date*: 2005-03-18 |
Sponsor Name:Canadian Cardiovascular Collaboration, Population Health Research Institute, McMaster University | ||
Full Title: PeriOperative ISchemic Evaluation study | ||
Medical condition: Perioperative cardiac events frequently complicate non-cardiac surgery resulting in significant morbidity, mortality and cost. There is no clear evidence from RCTs on how to lower perioperative ca... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002828-33 | Sponsor Protocol Number: ICRC-ICIT-01 | Start Date*: 2012-10-10 |
Sponsor Name:Fakultní nemocnice u sv. Anny v Brně | ||
Full Title: RANDOMIZED, MULTICENTRIC STUDY COMPARING THE EFFECT OF TWO REGIMENS OF COMBINED IMMUNOSUPPRESIVE THERAPY IN THE TREATMENT OF INFLAMMATORY CARDIOMYOPATHY CZECH-ICIT (CZECH INFLAMMATORY CARDIOMYOPATH... | ||
Medical condition: Patients with endomyocardial biopsy (EMB) proven inflammatory cardiomyopathy (ICM) defined by EMB established presence of myocardial inflammation and absence of cardiotropic infectious agents estab... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002859-41 | Sponsor Protocol Number: PVB/0011 | Start Date*: 2005-10-14 | |||||||||||
Sponsor Name:HAL Allergy B.V. | |||||||||||||
Full Title: Open-label, blinded endpoint, randomized, parallel treatment study to compare the clinical efficacy of PURETHAL® Bee and Alutard SQ Bee. | |||||||||||||
Medical condition: Patients with previous systemic reaction to honeybee sting (Müller stage I-III) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003529-17 | Sponsor Protocol Number: ARCADIA | Start Date*: 2008-11-17 | |||||||||||
Sponsor Name:IST. DI RICERCHE FARMACOLOG. M. NEGRI | |||||||||||||
Full Title: A PROSPECTIVE, RANDOMIZED, OPEN LABEL, BLINDED END-POINT (PROBE) TRIAL TO EVALUATE WHETHER, AT COMPARABLE BLOOD PRESSURE CONTROL, ACE INHIBITOR THERAPY MORE EFFECTIVELY THAN NON RAS INHIBITOR THERA... | |||||||||||||
Medical condition: End stage renal disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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