- Trials with a EudraCT protocol (130)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
130 result(s) found for: Elective Surgical Procedure.
Displaying page 1 of 7.
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 (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000566-36 | Sponsor Protocol Number: 14072010 | Start Date*: 2011-09-20 | |||||||||||
Sponsor Name:Hannu Kokki | |||||||||||||
Full Title: Laskimoon annetun ketoprofeenin ja deksketoprofeenin aiheuttama kirvely | |||||||||||||
Medical condition: Potilaat, joille on tarkoitus tehdä ei-päivystyksellinen toimenpide, ja joilla on tarkoitus käyttää laskimoon annettavaa ketoprofeenia ennakoivana kipulääkityksenä. Potilaiden tulee kuulua anestesi... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Ongoing) | |||||||||||||
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 |
EudraCT Number: 2010-019427-58 | Sponsor Protocol Number: 400-10-001 | Start Date*: 2010-09-08 | |||||||||||
Sponsor Name:Omrix Biopharmaceuticals Ltd | |||||||||||||
Full Title: A Phase III Randomized, Controlled, Superiority Study Evaluating the Fibrin Pad Versus Standard of Care Treatment in Controlling Parenchymal Bleeding During Elective Hepatic Surgery | |||||||||||||
Medical condition: Subjects undergoing elective, open, hepatic surgery during which a resection plane is created and wherein an appropriate Target Bleeding Site is identified. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005701-43 | Sponsor Protocol Number: PROP-001-CP3 | Start Date*: 2013-04-11 | |||||||||||
Sponsor Name:Fresenius Kabi Deutschland GmbH | |||||||||||||
Full Title: Therapeutic Equivalence Study of Propofol Using Target-Controlled Infusion of Propofol 2% (20 mg/mL) MCT Fresenius Compared with Diprivan® 20 mg/mL (AstraZeneca) in Patients Undergoing Elective Sur... | |||||||||||||
Medical condition: Elective minor Surgery | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
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: 2015-001788-37 | Sponsor Protocol Number: HCA-2015-2 | Start Date*: 2015-06-29 | ||||||||||||||||
Sponsor Name:Heart Center Co. Tampere University Hospital | ||||||||||||||||||
Full Title: Effects of volume changes to the plethysmography signal on major surgery patients | ||||||||||||||||||
Medical condition: Patients scheduled for elective CABG (Coronary artery bypass surgery). Patients scheduled for elective open major abdominal surgery (gastrointestinal surgery). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014346-28 | Sponsor Protocol Number: 02273917 | Start Date*: 2009-09-28 | |||||||||||
Sponsor Name:Erasme hospital | |||||||||||||
Full Title: Timing of intubation in a modified rapid sequence induction with remifentanil | |||||||||||||
Medical condition: The aim of the trial is to determine the timing for orotracheal intubation using the studied combination of products (Ultiva + Diprivan). | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001155-22 | Sponsor Protocol Number: Lap2014NMB | Start Date*: 2014-05-22 | ||||||||||||||||
Sponsor Name:Mona Ring Gätke | ||||||||||||||||||
Full Title: Muscle relaxation during open upper abdominal surgery -can the surgical conditions be optimized? (The laparotomy study) | ||||||||||||||||||
Medical condition: The aim of the study is to investigate if intense NMB improves surgical conditions during operation in patients scheduled for elective open upper abdominal surgery. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005846-36 | Sponsor Protocol Number: HGKKRWPHD | Start Date*: 2012-07-31 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Gastroenterology MIDT | ||||||||||||||||||||||||||||||||||||||
Full Title: Safe evaluation of obstructive crohns disease using bloodflow Time-intensity curves and Elastography correlated to Neutrocytes and collagen counts and biomechanical properties Obtained in Stenotic ... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Crohns Disease undergoing elective surgery for intestinal stenosis. | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005279-32 | Sponsor Protocol Number: NeuroMorfeo - FARM6FKJKK | Start Date*: 2007-12-10 | |||||||||||
Sponsor Name:A.O. San Gerardo di Monza | |||||||||||||
Full Title: ANESTHESIOLOGICAL STRATEGIES IN ELECTIVE CRANIOTOMY: RANDOMIZED, EQUIVALENCE, OPEN TRIAL | |||||||||||||
Medical condition: Study population. This is a multicenter randomized, open label, controlled trial, utilizing an equivalence design and evaluating three different anesthesiological strategies in patients undergoin... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002528-10 | Sponsor Protocol Number: SIVAA01 | Start Date*: 2017-07-06 |
Sponsor Name:Vestfold Hospital Trust | ||
Full Title: TOF trial: A randomized double blinded controlled Trial comparing low dose Of sugammadex and neostigmine aFter use of rocuronium during general anesthesia in patients undergoing non-cardiac surgery | ||
Medical condition: The study population will include all patients >18 years scheduled for an elective surgical procedure undergoing general anesthesia with intravenous drugs and non-depolarizing NMBA (rocuronium), wi... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-007987-40 | Sponsor Protocol Number: KetaminaEsse | Start Date*: 2008-12-29 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA | ||||||||||||||||||
Full Title: Low dose intravenous ketamine (S) associated to thoracic epidural analgesia: effects on the post-thoracotomy pain syndrome (PTPS) | ||||||||||||||||||
Medical condition: All patients that will undergo to an elective thoracotomic surgery in the Hospital Maggiore della Carita` of Novara for a 12 months period. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000922-31 | Sponsor Protocol Number: Cognitivefunction2011001 | Start Date*: 2011-04-18 | |||||||||||
Sponsor Name:Karolinska Institutet | |||||||||||||
Full Title: Patients´ recovery day 0-3 after short-stay elective surgery – a pilot study comparing desflurane and propofol TCI as main anaesthetics. | |||||||||||||
Medical condition: Patients undergoing elective general anaesthesia for breat surgery | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018480-42 | Sponsor Protocol Number: 550904 | Start Date*: 2010-11-12 | ||||||||||||||||
Sponsor Name:Baxter Innovations GmbH | ||||||||||||||||||
Full Title: A RANDOMIZED, CONTROLLED, MULTICENTER PHASE 2 STUDY TO EVALUATE THE EFFICACY AND SAFETY OF FIBRIN SEALANT VH S/D 500 S-APR (TISSEEL) FOR HEMOSTASIS IN SUBJECTS UNDERGOING HEPATIC RESECTION | ||||||||||||||||||
Medical condition: Hemostasis in hepatic resection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002961-21 | Sponsor Protocol Number: NS918 | Start Date*: 2018-11-09 |
Sponsor Name:UZ Leuven | ||
Full Title: The effect of deep neuromuscular block and reversal with sugammadex on surgical conditions and perioperative morbidity in shoulder surgery using a deltopectoral approach | ||
Medical condition: Subject undergoing elective or semi-elective surgery to the gleno-humeral joint or the proximal humerus using a deltoideo-pectoral approach. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022290-34 | Sponsor Protocol Number: 10-001 | Start Date*: 2010-12-07 |
Sponsor Name:Pharmecosse | ||
Full Title: An investigation of the efficacy of a single dose of insulin in the prevention of excessive cutaneous scarring in breast surgery patients | ||
Medical condition: Scarring arising from non cancer-related bilateral breast surgery | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000028-15 | Sponsor Protocol Number: TC-023-IM | Start Date*: 2007-01-26 |
Sponsor Name:Nycomed Danmark ApS | ||
Full Title: A randomised, open label, parallel-group, multi-centre trial to compare the efficacy and safety of TachoSil versus standard haemostatic treatment in the cardiovascular surgery | ||
Medical condition: Supportive haemostatic treatment in patients having elective surgery on the heart, the ascending aorta or arch, requiring pulmonary bypass procedure. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) FR (Completed) DK (Completed) IT (Completed) ES (Completed) | ||
Trial results: View results |
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: 2012-002648-26 | Sponsor Protocol Number: S54472 | Start Date*: 2013-10-16 | ||||||||||||||||||||||||||
Sponsor Name:UZ Leuven | ||||||||||||||||||||||||||||
Full Title: Exploratory Propofol Dose Finding Study In Neonates. | ||||||||||||||||||||||||||||
Medical condition: Investigation of the most effective intravenously administered single propofol dose for successful INSURE prodecure and for (semi-)elective intubation of neonates in non-INSURE conditions (e.g. sur... | ||||||||||||||||||||||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
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