- Trials with a EudraCT protocol (628)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (11)
628 result(s) found for: Heart surgery.
Displaying page 8 of 32.
EudraCT Number: 2016-004264-19 | Sponsor Protocol Number: NEODEX2 | Start Date*: 2017-04-05 |
Sponsor Name:Uppsala County Council | ||
Full Title: Anesthesia with dexmedetomidine and fentanyl for neonatal surgery. A pilot study. | ||
Medical condition: The state of anesthesia intraoperatively and pain postoperatively | ||
Disease: | ||
Population Age: Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-002090-12 | Sponsor Protocol Number: Ilocard | Start Date*: 2009-03-04 | |||||||||||
Sponsor Name:Hospital of the university of munich | |||||||||||||
Full Title: Effect of Iloprost inhalation before and during extracorporeal circulation (ECC) on perioperative morbidity and outcome in high risk cardiac surgical patients | |||||||||||||
Medical condition: In this study effects of the intra operative, prophylactic inhalation of Iloprost (Ventavis) before and during extracorporal circulation on perioperative morbidity and outcome in high risk cardiac ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-005144-14 | Sponsor Protocol Number: 01-CARDIONIDO | Start Date*: 2018-04-12 |
Sponsor Name:Dr. Forteza Gil | ||
Full Title: Comparative study of two types of cardioplegia during cardiac surgery in the adult patient | ||
Medical condition: Cardiac surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002926-35 | Sponsor Protocol Number: 080716CT | Start Date*: 2017-01-16 | |||||||||||
Sponsor Name:Alder Hey Children's Foundation NHS Trust | |||||||||||||
Full Title: Pharmacokinetics of post-operative Cefuroxime in infants undergoing cardiac surgery | |||||||||||||
Medical condition: post operative paediatric cardiac patients | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004446-42 | Sponsor Protocol Number: AIR | Start Date*: 2014-02-09 |
Sponsor Name:Skåne University Hospital | ||
Full Title: THE IMPORTANCE OF ALBUMIN INFUSION RATE FOR PLASMA VOLUME EXPANSION FOLLOWING MAJOR ABDOMINAL SURGERY | ||
Medical condition: Post operative patients who have been subjected to either a non-emergant Whipple operation or major gynecological cancer surgery ( including resection of ovaries, uterus, adnexa, oment and lymph ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004906-12 | Sponsor Protocol Number: ASK-3-2011 | Start Date*: 2011-11-07 | |||||||||||
Sponsor Name:Erling Bjerregaard Pedersen, Medicinsk forskningsafsnit, Regionshospitalet Holstebro | |||||||||||||
Full Title: Effect of hydroxyethyl starch on renal handling of sodium and water, vasoactive hormones,biomarkers and the circulatory system in patients undergoing hip replacement surgery | |||||||||||||
Medical condition: Patients undergoing hip replacement in spinal anesthesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002443-15 | Sponsor Protocol Number: ICAF-BETA | Start Date*: 2017-09-20 | |||||||||||
Sponsor Name:York Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Improving cardiac function in high-risk surgical patients: exercise testing, biomarkers and beta-blockade | |||||||||||||
Medical condition: Impaired VE/CO2 on cardio pulmonary exercise testing | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003942-33 | Sponsor Protocol Number: M13-796 | Start Date*: 2013-05-03 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Phase 2b, Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Trial of Multiple Dosing Regimens of ABT-719 for the Prevention of Acute Kidney Injury in Subjects Undergoing High Risk... | |||||||||||||
Medical condition: Acute Kidney Injury | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001835-20 | Sponsor Protocol Number: OZBS12.15060 | Start Date*: 2016-01-20 |
Sponsor Name:Erasmus MC | ||
Full Title: Morphine intravenous vs. paracetamol intravenous after cardiac surgery in neonates and infants. | ||
Medical condition: congenital cardiac defects | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003320-23 | Sponsor Protocol Number: AC-055H301 | Start Date*: 2017-10-11 | ||||||||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd | ||||||||||||||||||
Full Title: Prospective, multi-center, double-blind, randomized, placebo-controlled, parallel-group study assessing the efficacy and safety of macitentan in Fontan-palliated adult and adolescent subjects. | ||||||||||||||||||
Medical condition: Congenital Heart Failure | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) DK (Completed) FR (Completed) PL (Completed) IE (Completed) CZ (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-000024-13 | Sponsor Protocol Number: aspirin v1 | Start Date*: 2006-03-19 |
Sponsor Name:Cardiff and Vale NHS Trust | ||
Full Title: Does Aggressive management with early high dose aspirin reduce the hypercoagulability of platelets following coronary artery bypass grafting? | ||
Medical condition: Aspirin is an antiplatelet drug that affects the ability of platelets in the blood to bind together and form clots. It is used routinely in patients with or at risk of heart disease and after surg... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-002936-34 | Sponsor Protocol Number: iPROVE-O2-16 | Start Date*: 2017-01-30 |
Sponsor Name:Francisco Javier Belda Nacher | ||
Full Title: Effects on surgical site infection of an individualized perioperative openlung ventilatory strategy with high versus conventional inspiratory oxygen fraction (iPROVEO2). A comparative, prospective,... | ||
Medical condition: The study population will be patients who are scheduled for major abdominal (laparotomy and laparoscopic) surgery under general anaesthesia. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000656-18 | Sponsor Protocol Number: 2042015 | Start Date*: 2018-11-09 | |||||||||||
Sponsor Name:SINTETICA SA | |||||||||||||
Full Title: Randomized, multi-center, double-blind, two-armed, parallel active groups, prospective trial, to evaluate, in pediatric population undergoing 'Calcaneo stop' surgery or Inguinal hernia repair, the ... | |||||||||||||
Medical condition: Pediatric patients undergoing surgery of flatfoot or inguinal hernia | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) ES (Restarted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022791-31 | Sponsor Protocol Number: D01092010AZNTG | Start Date*: Information not available in EudraCT | |||||||||||||||||||||||||||||||
Sponsor Name:University Erlangen-Nuremberg | |||||||||||||||||||||||||||||||||
Full Title: Contrast sensitivity of patients with normal tension glaucoma by application of Azarga® | |||||||||||||||||||||||||||||||||
Medical condition: The effect of AZARGA(R) on the central and spacial-temporal contrast sensitivity of patients with normal tension glaucoma will be examined. Healthy controls are required to prove the disease specif... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002078-38 | Sponsor Protocol Number: SU/2016/6033 | Start Date*: 2017-12-06 | |||||||||||||||||||||
Sponsor Name:University Hospitals Bristol NHS Foundation Trust | |||||||||||||||||||||||
Full Title: Effectiveness, cost effectiveness and safety of gabapentin versus placebo as an adjunct to multimodal pain regimens in surgical patients: A placebo controlled randomised controlled trial with blind... | |||||||||||||||||||||||
Medical condition: Post surgery pain management | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001135-27 | Sponsor Protocol Number: 000000 | Start Date*: 2020-09-11 | |||||||||||||||||||||||||||||||
Sponsor Name:University of Oxford / Clinical Trials and Research Governance | |||||||||||||||||||||||||||||||||
Full Title: Pre-operative 5-Aminolevulinic acid to activate haem oxygenase to improve outcomes in cardiac surgery: A dose finding study | |||||||||||||||||||||||||||||||||
Medical condition: Cardioprotection for coronary artery bypass graft surgery | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002274-41 | Sponsor Protocol Number: MCL-metoprolol-CR | Start Date*: 2013-07-11 |
Sponsor Name:Medisch Centrum Leeuwaarden | ||
Full Title: The effect of Roux-en-Y gastric bypass on the rate and extent of absorption of metoprolol from a controlled release tablet in female bariatric patient volunteers: a single oral dose study before an... | ||
Medical condition: Roux-en-Y gastric bypass | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002260-10 | Sponsor Protocol Number: MCL-metoprolol-IR | Start Date*: 2013-07-11 |
Sponsor Name:Medisch Centrum Leeuwarden | ||
Full Title: The effect of Roux-en-Y gastric bypass on the rate and extent of absorption of metoprolol from an immediate release tablet in female bariatric patient volunteers: a single oral dose study before an... | ||
Medical condition: Roux-en-Y gastric bypass | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001094-16 | Sponsor Protocol Number: PROACT | Start Date*: 2017-08-08 | |||||||||||
Sponsor Name:South Tees NHS Foundation Trust | |||||||||||||
Full Title: Preventing cardiac damage in patients treated for breast cancer and lymphoma: a phase 3 Randomised, Open label, blinded endpoint, trial of enalapril to prevent Anthracycline-induced CardioToxicity ... | |||||||||||||
Medical condition: Prevention of cardiotoxicity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003893-46 | Sponsor Protocol Number: NA | Start Date*: 2009-11-03 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:KULeuven and University Hospitals Leuven (Leuven Lung Transplant Group) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: AZITHROMYCIN IN BRONCHIOLITIS OBLITERANS SYNDROME | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: - Chronic rejection at 1 and 2 year post-lung transplantation - Mortality at 1 and 2 year post-lung transplantation - Acute rejection rate at 1 and 2 post-lung transplantation - Infection rate at 1... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
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