- Trials with a EudraCT protocol (261)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
261 result(s) found for: Cardiac surgical procedures.
Displaying page 1 of 14.
EudraCT Number: 2015-004485-28 | Sponsor Protocol Number: 38RC15.214 | Start Date*: 2016-01-18 | |||||||||||
Sponsor Name:Centre Hospitalier Universitaire de Grenoble | |||||||||||||
Full Title: | |||||||||||||
Medical condition: Patients should be operated for cardiac surgery with cardiac bypass and in sinus rhythm, and for which the fact of the existence of impaired left ventricular function or the heaviness of the surgic... | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000100-40 | Sponsor Protocol Number: f7card-1610 | Start Date*: 2004-08-18 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: Estudio multicentrico. aleatorizado, doble ciego, controlado con placebo y con escalada de dosis sobre la seguridad y la eficacia del factor VII recombinante activado (rFVIIa/NovoSeven) en el trata... | |||||||||||||
Medical condition: Enfermedad de corazon/cirugia cardiaca. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) SE (Prematurely Ended) GB (Prematurely Ended) IT (Prematurely Ended) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000459-10 | Sponsor Protocol Number: PADIT | Start Date*: 2014-06-10 | |||||||||||
Sponsor Name:Population Health Research Institute (PHRI) | |||||||||||||
Full Title: A cluster Crossover Trial Comparing Conventionl vs Incremental Antibiotic Therapy for the Prevention or Arrhytmia Device Infection | |||||||||||||
Medical condition: high-risk patients undergoing arrhythmia device procedures | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003088-76 | Sponsor Protocol Number: 11-170 | Start Date*: 2014-07-14 |
Sponsor Name:Clinical Evaluation Research Unit (CERU) | ||
Full Title: SodiUm SeleniTe Adminstration IN Cardiac Surgery surgery (SUSTAIN CSX®-trial) - A randomized controlled trial of high dose sodium-selenite administration in high risk cardiac surgical patients | ||
Medical condition: Selenium is a key component of a number of selenoproteins which protect against oxidative stress and is well recognised for its prominent role in immune defence. Selenoproteins have the potential t... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001756-19 | Sponsor Protocol Number: MTP-2019-01 | Start Date*: 2019-12-11 |
Sponsor Name:María de los Ángeles Tena Pajuelo (Investigador independiente) | ||
Full Title: MULTI-CENTER, DOUBLE-BLIND, CONTROLLED, PARALLEL AND RANDOMIZED STUDY TO COMPARE THE EFFECTIVENESS OF 0.1 ΜG / KG / MIN OF LEVOSIMENDAN VERSUS PLACEBO IN THE POSTOPERATIVE OF CARDIAC PROGRAMMED SUR... | ||
Medical condition: Patients who have preoperatively severe left ventricular dysfunction (LVEF ≤ 35%) and will be scheuled for cardiac surgery on cardiopulmonary bypass. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000177-39 | Sponsor Protocol Number: Linea7-2013/06-APPEAR | Start Date*: 2014-07-17 |
Sponsor Name:IRCCS Policlinico San Donato | ||
Full Title: Albumin vs. Plasma for PEdiAtric pRiming (APPEAR) trial | ||
Medical condition: Congenital cardiac diseases needing surgical correction requiring intervention with extracorporeal circulation | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002207-17 | Sponsor Protocol Number: D-PLEX-302 | Start Date*: 2020-07-14 | |||||||||||
Sponsor Name:PolyPid Ltd. | |||||||||||||
Full Title: A Phase III, Prospective, Multinational, Multicenter, Randomized, Parallel Controlled, Two arms, Single Blind, Study to Assess the Efficacy and Safety of D-PLEX Administered Concomitantly with the ... | |||||||||||||
Medical condition: Prevention of Post-Cardiac Surgery Sternal Infections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004894-96 | Sponsor Protocol Number: 2011-10-03 | Start Date*: 2012-03-20 | ||||||||||||||||
Sponsor Name:Mikko Hippeläinen [...] | ||||||||||||||||||
Full Title: ORAL ABSORPTION OF OXYCODONE AFTER CARDIAC BYPASS SURGERY | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000201-24 | Sponsor Protocol Number: O3Cardio | Start Date*: 2018-08-01 | ||||||||||||||||
Sponsor Name:Bernardino Clavo - Hospital Dr. Negrín | ||||||||||||||||||
Full Title: Effectiveness and cost-effectiveness of Ozone therapy in patients with ischemic heart disease refractory to medical and surgical treatment: Randomized, triple-blind clinical trial. | ||||||||||||||||||
Medical condition: Ischemic heart disease refractory to medical and surgical treatment. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000404-28 | Sponsor Protocol Number: CRAD001ANO05 | Start Date*: 2016-07-20 | |||||||||||
Sponsor Name:Novartis Norge AS | |||||||||||||
Full Title: 5, 6 or 7 year follow-up control after the SCHEDULE study (SCANDINAVIAN HEART TRANSPLANT EVEROLIMUS DE NOVO STUDY WITH EARLY CNI AVOIDANCE) Title of the original SCHEDULE study: A controlled ran... | |||||||||||||
Medical condition: Heart transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003831-20 | Sponsor Protocol Number: 2008/27 | Start Date*: 2008-11-18 | |||||||||||
Sponsor Name:Hopital Foch | |||||||||||||
Full Title: Comparaison de l'effet de deux doses d'Acide Tranexamique sur les besoins transfusionnels en chirurgie cardiaque | |||||||||||||
Medical condition: cardiac surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-009115-22 | Sponsor Protocol Number: IGG-LR-08 | Start Date*: 2009-05-04 | |||||||||||
Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
Full Title: Fenoldopam mesilate efficacy to control splancnic ischemia during cardiopulmonary bypass in pediatric patients | |||||||||||||
Medical condition: cardiac surgery with CPB | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013074-41 | Sponsor Protocol Number: CRAD001ANO02 | Start Date*: 2009-11-10 | |||||||||||
Sponsor Name:Novartis Norge AS | |||||||||||||
Full Title: A controlled randomized open-label multicentre study evaluating if early initiation of everolimus (Certican®)and early elimination of cyclosporine (Sandimmun Neoral®) in de novo heart transplant re... | |||||||||||||
Medical condition: Heart transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000442-21 | Sponsor Protocol Number: RC17_0029 | Start Date*: 2017-09-12 | |||||||||||
Sponsor Name:CHU de Nantes | |||||||||||||
Full Title: Effects of perioperative administration of dexamethasone on postoperative complications and mortality after non-cardiac major surgery : a randomized, multicentre, double blind, study | |||||||||||||
Medical condition: non-cardiac major surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
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: 2013-003557-24 | Sponsor Protocol Number: 400-12-004 | Start Date*: 2014-04-02 |
Sponsor Name:Ethicon Inc | ||
Full Title: A Prospective, Randomised, Controlled, Study Evaluating the Safety and Effectiveness of EVARREST® Sealant Matrix in Controlling Mild or Moderate Hepatic Parenchyma or Soft Tissue Bleeding During O... | ||
Medical condition: Mild or moderate hepatic parenchyma or soft tissue bleeding during open, abdominal, retroperitoneal, pelvic and thoracic (non-cardiac) surgery | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005920-16 | Sponsor Protocol Number: CHUB-930105 | Start Date*: 2012-02-06 |
Sponsor Name:Association Hospitalière CHU Brugmann | ||
Full Title: Prospective, controled, randomized, double blind monocentric study evaluating the efficacy of the basic component of colloids (corn versus potato) on perioperative blood losses in elective cardiac ... | ||
Medical condition: Elective cardiac surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-001759-17 | Sponsor Protocol Number: FGTW2101 | Start Date*: 2022-10-04 | |||||||||||
Sponsor Name:Laboratoire français du Fractionnement et des Biotechnologies (LFB BIOTECHNOLOGIES) | |||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo-controlled, parallel, phase 3 study to assess the efficacy and safety of fibrinogen concentrate (FGTW) in the management of bleeding in patients und... | |||||||||||||
Medical condition: Bleeding in patients undergoing complex cardiac surgery (involving CPB) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) ES (Ongoing) DE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023093-39 | Sponsor Protocol Number: SIRS | Start Date*: 2011-09-08 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE POLICLINICO CONSORZIALE | |||||||||||||
Full Title: Steroids In caRdiac Surgery Trial | |||||||||||||
Medical condition: Require CPB for any cardiac surgical procedure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) CZ (Completed) ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005291-34 | Sponsor Protocol Number: NL41467 | Start Date*: 2014-02-14 | ||||||||||||||||
Sponsor Name:AMC, Amsterdam | ||||||||||||||||||
Full Title: Perioperative intravenous insulin, GIK or GLP-1 treatment in DM | ||||||||||||||||||
Medical condition: Patients with diabetes mellitus type 2 who will undergo non-cardiac surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
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