- Trials with a EudraCT protocol (816)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18)
816 result(s) found for: Cardiac Surgery.
Displaying page 2 of 41.
EudraCT Number: 2020-000087-26 | Sponsor Protocol Number: 2019/09 | Start Date*: 2020-04-16 | |||||||||||||||||||||
Sponsor Name:CMC AMBROISE PARE | |||||||||||||||||||||||
Full Title: Time to transit Recovery After treatment with Naloxegol in cardiac Surgery Intensive care Trial | |||||||||||||||||||||||
Medical condition: ileus after cardiac surgery | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002752-20 | Sponsor Protocol Number: LAN_POAF_01 | Start Date*: 2020-12-17 | |||||||||||
Sponsor Name:Medical University of Vienna | |||||||||||||
Full Title: A prospective, randomized, double- blind, placebo- controlled study to evaluate the efficacy of Landiolol hydrochloride for prevention of atrial fibrillation in patients undergoing cardiac surgery | |||||||||||||
Medical condition: Perioperative atrial fibrillation (POAF) is the most common arryhthmia after cardiac surgery with incidences ranging from 20% to 40%, depending on various patient's risk factors and the type of sur... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002541-11 | Sponsor Protocol Number: P170912J | Start Date*: 2019-06-06 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Prevention of post-operative Atrial Fibrillation by BOTulinum toxin injections into epicardial fat pads around pulmonary veins in patients undergoing cardiac surgery | |||||||||||||
Medical condition: Adult patients with indication for conventional cardiac surgery (CABG, aortic replacement, or ascending aorta surgery) will be eligible | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001481-32 | Sponsor Protocol Number: Effetto anti-infiammatorio insulin | Start Date*: 2006-09-21 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE POLICLINICO CONSORZIALE | |||||||||||||
Full Title: Evaluation of the anti-inflammatory effect of continous insulin infusion in non-diabetic patients undergoing cardia surgery | |||||||||||||
Medical condition: Patients candidate to cardiac surgery | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021263-33 | Sponsor Protocol Number: 3001101 | Start Date*: 2011-05-24 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Sykehuset i Vestfold HF | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: PERIOPERATIVE LEVOSIMENDAN INFUSION IN PATIENTS WITH HEART FAILURE UNDERGOING NON-CARDIAC SURGERY: A PROSPECTIVE, RANDOMISED, PLACEBO-CONTROLLED, DOUBLE-BLIND, MULTICENTER STUDY | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients with serious cardiac failure scheduled for non-cardiac surgery | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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: 2019-001086-32 | Sponsor Protocol Number: 19-001_AMG | Start Date*: 2020-01-02 |
Sponsor Name:RWTH Aachen University represented by the Rector himself, represented by the Dean of the Medical Faculty | ||
Full Title: ADVANCE-CSX Pilot – Antioxidant Treatment with Vitamin C in Cardiac Surgery Patients – a Clinical Pilot Study | ||
Medical condition: Patients undergoing high-risk open-heart surgery with the use of cardiopulmonary bypass (CPB) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-018301-11 | Sponsor Protocol Number: 29421073 | Start Date*: Information not available in EudraCT |
Sponsor Name:Centre chirurgical Marie Lannelongue | ||
Full Title: STUDY OF TRANAXAMIC ACID DOSAGE IN PEDIATRIC CARDIAC SURGERY | ||
Medical condition: DOSAGE OF ACID TRANEXAMIC ACID IN BLOOD SAMPLES DURING PAEDIATRIC CARDIAC SURGERY | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004343-80 | Sponsor Protocol Number: 545.12 | Start Date*: 2012-09-20 | |||||||||||
Sponsor Name:OSPEDALE PEDIATRICO BAMBINO GESU' DI ROMA | |||||||||||||
Full Title: STUDY PHASE III, RANDOMIZED, DOUBLE-BLIND CONTROLLED TO EVALUATE THE EFFECTIVENESS OF FUROSEMIDE IN CONTINUOUS INFUSION VS ethacrynic acid IN CONTINUOUS INFUSION IN CHILDREN SUBJECT TO A heart sur... | |||||||||||||
Medical condition: ALL CHILDREN AGE 'LESS THAN 10 YEARS OF AGE' WITH CONGENITAL HEART PROCEDURE SUBJECT TO cardiac surgery in whom the diuretic ARE GIVEN IN ACCORDANCE WITH THE FOLLOWING CONTINUOUS INFUSION PROTOCOL ... | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013226-17 | Sponsor Protocol Number: AustrNHMRVID436677 | Start Date*: 2009-09-29 |
Sponsor Name:Plymouth Hospitals NHS Trust | ||
Full Title: The ENIGMA-II Trial. Nitrous oxide anaesthesia and cardiac morbidity after major surgery: a randomised controlled trial | ||
Medical condition: The study investigates standard anaesthesia for surgery. There is no single specific 'disease' rather there is a population of patients requiring anaesthesia to permit surgery. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000223-17 | Sponsor Protocol Number: P07.xxx | Start Date*: 2008-02-26 |
Sponsor Name:M.S. Arbous | ||
Full Title: PRACDICAL Study Prevention and Risk factors of Arterial Complications in DIabetics after non-CArdiac surgicaL interventions | ||
Medical condition: Diabetes Mellitus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002672-13 | Sponsor Protocol Number: CRHACS | Start Date*: 2021-03-18 | |||||||||||
Sponsor Name:ALMA MATER STUDIORUM UNIVERSITà DI BOLOGNA | |||||||||||||
Full Title: CPAP Reduces Hypoxemia After Cardiac Surgery (CRHACS Trial). A randomized controlled trial | |||||||||||||
Medical condition: Hypoxemia after cardiac surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003164-62 | Sponsor Protocol Number: 1976 | Start Date*: 2007-01-22 |
Sponsor Name:University Hospital Birmingham | ||
Full Title: Metabolic Support with Perhexilene to Protect Myocardium undergoing Coronary Artery Surgery | ||
Medical condition: Patients undergoing coronary artery bypass surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003053-24 | Sponsor Protocol Number: 614 | Start Date*: 2006-05-18 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Prophylaxis with fenoldopam in cardiac surgery patients at high risk of postoperative renal failure | |||||||||||||
Medical condition: cardiac surgery patients at high risk of postoperative renal failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004871-11 | Sponsor Protocol Number: ULA02 | Start Date*: 2019-09-05 | |||||||||||
Sponsor Name:Cardiorentis AG | |||||||||||||
Full Title: RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED DOSE ESCALATION STUDY OF ULARITIDE FOLLOWED BY A 42-HOUR INFUSION FOR THE TREATMENT OF ACUTE KIDNEY INJURY (AKI) IN PATIENTS POST CARDIAC SURGERY | |||||||||||||
Medical condition: Acute kidney injury in patients post cardiac surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008354-23 | Sponsor Protocol Number: ECAL-CCPB-08-07 | Start Date*: 2009-04-30 |
Sponsor Name:Cubist Pharmaceuticals,INC | ||
Full Title: CONSERVTM – 2 (Clinical Outcomes and Safety Trial to Investigate Ecallantide’s Effect on Reducing Surgical Blood Loss Volume) – A Phase 2 Randomized Double-Blind Active-Controlled Study in Subjects... | ||
Medical condition: Reduction of blood loss in subjects exposed to CPB during cardiac surgery at high risk for bleeding | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PL (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-002756-21 | Sponsor Protocol Number: 1663/2020 | Start Date*: 2021-02-23 |
Sponsor Name:Department of Cardiothoracic Anesthesia and Intensive Care Medicine, Medical University of Vienna | ||
Full Title: Plasma Pharmacokinetics of Prophylactic Cefazolin Administered for Cardiac Surgery: Comparison of Cardiopulmonary Bypass Priming with Additive Human Albumin 20% vs.Pure Crystalloid Priming: A singl... | ||
Medical condition: This is a pharmacokinetic trial for patients undergoing cardiac surgery. It will be investigated whether cardiopulmonary bypass priming substituted with human albumin 20% has an effect on the pharm... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006480-23 | Sponsor Protocol Number: 10,176 | Start Date*: 2007-10-12 |
Sponsor Name:University Hospitals of Leicester | ||
Full Title: Autologous Bone Marrow-Derived Cells for Cardioprotection During Heart Surgery | ||
Medical condition: Improvement of cardioprotection during elective coronary artery bypass graft surgery using the patients own bone marrow cells. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-004191-35 | Sponsor Protocol Number: AGO/2013/011 | Start Date*: 2014-11-28 | ||||||||||||||||
Sponsor Name:Ghent University Hospital | ||||||||||||||||||
Full Title: Evaluation of the effects and plasma concentration of the potent platelet inhibitor ticagrelor, after crushed and non-crushed intake, after semi-urgent coronary bypass and in patients after cardiac... | ||||||||||||||||||
Medical condition: Group A: Patients who received CPR because of cardiac arrest. Group B: Patients in need of semi-urgent coronary bypass surgery, allowing interrupting the administration of ticagrelor 3 days before ... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-015013-46 | Sponsor Protocol Number: AnaesthesiaResearch024 | Start Date*: 2009-12-14 |
Sponsor Name:Alfred Health | ||
Full Title: The ATACAS Trial: Aspirin and Tranexamic Acid for Coronary Artery Surgery Trial | ||
Medical condition: Coronary Artery Bypass Grafting | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) IT (Completed) | ||
Trial results: (No results available) |
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