- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9 result(s) found for: Aortic cross clamp.
Displaying page 1 of 1.
EudraCT Number: 2011-002643-10 | Sponsor Protocol Number: HCA-2011_1 | Start Date*: 2012-01-17 |
Sponsor Name:Heart Center Co. Tampere University Hospital | ||
Full Title: Intracoronary administration of levosimendan in cardiac surgery patients | ||
Medical condition: Dysfunction after opening of aortic cross-clamp in patients undergoing aortic valve and coronary artery bypass (AVR+CABG) operation. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003776-40 | Sponsor Protocol Number: CL-N-CSM-AV-III/05/12 | Start Date*: 2013-11-08 |
Sponsor Name:Dr. Franz Köhler Chemie GmbH | ||
Full Title: A Prospective Randomized Double Blind Multicenter Phase III Study Comparing two Methods of Cardioplegia in Aortic Valve Surgery Custodiol-N versus Custodiol | ||
Medical condition: Patients with aortic valve disease and has to undergo aortic valve surgery +/- bypass surgery. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-003396-20 | Sponsor Protocol Number: MMUH-Conway01 | Start Date*: 2012-11-26 |
Sponsor Name:Cardiothoracic Surgery, Mater Misericordiae University Hospital | ||
Full Title: Is the optimal dose of preoperative statin associated with decreased end organ injury and better clinical outcome post cardiopulmonary bypass? | ||
Medical condition: Patient listed for open heart surgery involving cardiopulmonary bypass. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-002376-95 | Sponsor Protocol Number: RRK3535 | Start Date*: 2009-01-05 |
Sponsor Name:University Hospital Birmingham NHS Foundation Trust | ||
Full Title: Myocardial protection with Perhexiline in Left Ventricular Hypertrophy | ||
Medical condition: Patients with left ventricular hypertrophy undergoing aortic valve surgery (with or without coronary artery surgery) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006887-44 | Sponsor Protocol Number: RGHT000396 | Start Date*: 2007-06-19 | |||||||||||
Sponsor Name:Royal Group Hospitals Trust | |||||||||||||
Full Title: Non-invasive bed-side measurement of systemic endothelial function in patients undergoing abdominal aortic aneurysm repair; modulation by ascorbic acid | |||||||||||||
Medical condition: Abdominal Aortic Aneurysm | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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: 2022-001795-34 | Sponsor Protocol Number: CL-N-HTX-Paed-II/10/20 | Start Date*: 2023-01-30 | |||||||||||
Sponsor Name:Dr. Franz Köhler Chemie GmbH | |||||||||||||
Full Title: A prospective randomized single blind multicenter phase II study of organ perfusion with Custodiol-N compared with Custodiol in heart transplantation in children | |||||||||||||
Medical condition: Preservation of hearts prior to heart transplantation in children | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001112-29 | Sponsor Protocol Number: CL-N-HTX-CSM-III/04/12 | Start Date*: 2015-07-27 |
Sponsor Name:Dr. Franz Köhler Chemie GmbH | ||
Full Title: A Prospective, randomized, single blind, multicenter Phase III study of organ perfusion with Custodiol-N solution compared with Custodiol solution in Heart transplantation | ||
Medical condition: Patients that has to undergo (is suitable for) a heart transplantation | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-005992-81 | Sponsor Protocol Number: CL-N-CSM-III/01/08 | Start Date*: 2011-03-21 | |||||||||||
Sponsor Name:Dr. F. Köhler Chemie GmbH | |||||||||||||
Full Title: A Prospective Randomized Double Blind Multicenter Phase III Study Comparing two Methods of Cardioplegia in Coronary Artery Bypass Surgery Custodiol-N versus Custodiol | |||||||||||||
Medical condition: The study population will be selected from both genders with coronary artery disease (CAD) who are to undergo cardiopulmonary bypass for coronary artery bypass surgery. The ratio of incidence for b... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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