- Trials with a EudraCT protocol (717)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
717 result(s) found for: General surgery.
Displaying page 1 of 36.
EudraCT Number: 2005-001574-27 | Sponsor Protocol Number: MR-2005\01 | Start Date*: 2005-09-27 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PERUGIA | |||||||||||||
Full Title: Sevoflurane on cardiac surgery: vantage to use during CEC | |||||||||||||
Medical condition: general anestetic inalathory also during CEC | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016094-16 | Sponsor Protocol Number: AGO/2009/008 | Start Date*: 2010-02-04 | |||||||||||
Sponsor Name:University Hospital Ghent | |||||||||||||
Full Title: Sevoflurane-Remifentanil interaction: Multiple response surfaces, validation of calibration stimuli, validation of the intraoperative isobole concept and investigating remifentanil induced opioid t... | |||||||||||||
Medical condition: American Society of Anesthesia class I and II patients scheduled for surgery under general anesthesia. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002824-98 | Sponsor Protocol Number: ANE_HEPUNOX | Start Date*: 2016-10-20 | |||||||||||
Sponsor Name:Fundació Hospital Vall Hebron Institut de Recerca | |||||||||||||
Full Title: Comparison of three techniques in the management of the postoperatory acute pain, after a general anesthesia based on the control of the nociception. | |||||||||||||
Medical condition: Acute postoperative pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003515-44 | Sponsor Protocol Number: ACA-SPAI-04-22 | Start Date*: 2006-12-26 | |||||||||||
Sponsor Name:FRANCISCO JAVIER BELDA | |||||||||||||
Full Title: Cardioprotective effect of sevoflurane versus propofol used during anesthesia and the postoperative period in patients undergoing coronary bypass surgery. Impact on critical care unit stay. A doubl... | |||||||||||||
Medical condition: This study will evaluate the cardioprotective effects of sevoflurane versus propofol during anesthesia and sedation of patients undergoing coronary bypass surgery in terms of maintenance of cardiac... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023942-63 | Sponsor Protocol Number: 10-017 | Start Date*: 2011-01-17 | |||||||||||
Sponsor Name:Clinical Trials Center Aachen, University of Aachen | |||||||||||||
Full Title: The safety and feasibility of delivering xenon to patients before and after coronary artery bypass graft implantation: a pilot study Abbreviated study title: A pre- and post-Coronary Artery bypass... | |||||||||||||
Medical condition: The aim of this study is to determine whether xenon and remifentanil – as compared to sevoflurane and remifentanil – can be applied safely in patients after CABG implantation for the remaining surg... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005197-11 | Sponsor Protocol Number: SENC | Start Date*: 2015-04-24 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PAPA GIOVANNI XXIII | |||||||||||||
Full Title: Sugammadex and neurogical effects central | |||||||||||||
Medical condition: patient undergoing elective surgery for which has been indicated only the general anesthesia with tracheal intubation and curarization | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002978-62 | Sponsor Protocol Number: 2007/13 | Start Date*: 2009-03-18 | ||||||||||||||||
Sponsor Name:Hopital Foch | ||||||||||||||||||
Full Title: Influence de l’analgésie peropératoire (sufentanil administré selon les critères usuels ou rémifentanil administré par un système automatisé à partir de l’Index Bispectral) sur la consommation de m... | ||||||||||||||||||
Medical condition: general anesthesia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004555-79 | Sponsor Protocol Number: 16-115 | Start Date*: 2017-08-08 |
Sponsor Name:RWTH Aachen University represented by the Rector himself, represented by the Dean of the Medical Faculty | ||
Full Title: Impact of preoperative midazolam on outcome of elderly patients: a multicenter randomised controlled trial | ||
Medical condition: Under investigation are elderly patients (≥65 years of age) undergoing each kind of surgery with planned general or combined regional and general anaesthesia. Primary, we will investigate the posto... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
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: 2012-001886-33 | Sponsor Protocol Number: MK-8616-076-00 | Start Date*: 2012-10-30 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: Randomized, Controlled, Parallel Group, Double Blind Trial to Compare the Use of Deep or Standard Neuromuscular Blockade in Combination With Low or Standard Insufflation Pressures Using a 2x2 Fact... | |||||||||||||
Medical condition: Patients undergoing elective in-patient laparoscopic cholecystectomy procedures under general anesthesia with neuromuscular relaxation and active reversal of neuromuscular blockade | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) FI (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005773-21 | Sponsor Protocol Number: IBMS-SPB | Start Date*: 2016-05-10 | |||||||||||
Sponsor Name:INSTITUTO DE INVESTIGACIÓN SANITARIA LA FE | |||||||||||||
Full Title: Impact of the serratus plane block in pain and the use of opioids in breast surgery | |||||||||||||
Medical condition: Patients undergoing oncological surgery and/or breast reconstruction surgery | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004163-50 | Sponsor Protocol Number: FIBHGM-ECNC002-2013(CETSEVOREM) | Start Date*: 2014-04-29 | |||||||||||
Sponsor Name:Fundación para la Investigación Biomédica del Hospital | |||||||||||||
Full Title: Comparative, randomized, double-blind clinical trial on end-tidal concentration of sevoflurane associated to remifentanil required for insertion of the Supreme Laryngeal Mask vs. Pro-Seal Laryngea... | |||||||||||||
Medical condition: Patients requiring general anesthesia in whom the control of the airway is usually done with a supraglottic device. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000956-32 | Sponsor Protocol Number: 20022012 | Start Date*: 2012-06-28 |
Sponsor Name:St. Antonius Ziekenhuis | ||
Full Title: Pharmacokinetics of intravenous acetaminophen and its metabolites in morbidly obese patients | ||
Medical condition: Morbid obesity | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021022-35 | Sponsor Protocol Number: 0908125 | Start Date*: 2010-10-12 | ||||||||||||||||
Sponsor Name:CHU de Saint-Etienne | ||||||||||||||||||
Full Title: Effet of curarization under general anaesthesia on eye movements in non-strabismus children | ||||||||||||||||||
Medical condition: Healthy volunteer who will have a surgery requiring curare administration (amygdalectomy...) | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004737-37 | Sponsor Protocol Number: CORTERAS | Start Date*: 2021-11-16 | |||||||||||
Sponsor Name:Ziekenhuis Oost-Limburg | |||||||||||||
Full Title: The effect of corticosteroids on early recovery after major surgery in elderly patients_ CORTERAS STUDY | |||||||||||||
Medical condition: major surgery • off-pump coronary bypass surgery • on-pump coronary bypass surgery • Aortic Valve Replacement Mini Access Surgery • laparoscopic hemicolectomies • thoracoscopic lung resections • fe... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001139-98 | Sponsor Protocol Number: IC2021-07 | Start Date*: 2022-06-13 | ||||||||||||||||
Sponsor Name:Institut Curie | ||||||||||||||||||
Full Title: Opioid-Free versus Opioid-Based Anaesthesia for secondary free-flap reconstruction surgery of the breast: A phase III multicentric randomized controlled study | ||||||||||||||||||
Medical condition: Anaesthesia during secondary free flap reconstruction surgery of the breast. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002803-81 | Sponsor Protocol Number: TREX | Start Date*: 2020-04-03 | |||||||||||
Sponsor Name:IRCCS ISTITUTO GIANNINA GASLINI | |||||||||||||
Full Title: Neurodevelopmental outcome after standard dose sevoflurane versus low-dose sevoflurane/dexmedetomidine/remifentanil anaesthesia in young children | |||||||||||||
Medical condition: Children under the age of 2 years having surgery lasting at least 2 hours | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001646-10 | Sponsor Protocol Number: ANIMAL-523-2014-2569 | Start Date*: 2017-06-22 |
Sponsor Name:Uppsala University Hospital | ||
Full Title: Anesthesia Induced Hormonal Oliguria Trial | ||
Medical condition: Anaesthesia in adult patients undergoing general surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (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 (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019591-67 | Sponsor Protocol Number: 1008032 | Start Date*: 2010-06-01 | |||||||||||
Sponsor Name:CHU de SAINT-ETIENNE | |||||||||||||
Full Title: Pain assessment during general anesthesia : DOLANS Study | |||||||||||||
Medical condition: perioperative analgesia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
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