- Trials with a EudraCT protocol (5,833)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (321)
5,833 result(s) found for: Surgery.
Displaying page 5 of 292.
EudraCT Number: 2016-001584-36 | Sponsor Protocol Number: 2014-03-11 | Start Date*: 2016-06-01 |
Sponsor Name:Universitetssjukhuset Örebro | ||
Full Title: Is high oxygen concentration a riskfactor for postoperative complications? A prospective, randomized, singel blinded study in elderly patients undergoing vascular surgery | ||
Medical condition: Elective vascular surgery (peripheral vascular and aortic surgery) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000516-42 | Sponsor Protocol Number: CLX003-IMP-2-170121 | Start Date*: 2018-03-20 | ||||||||||||||||
Sponsor Name:Cell Therapy Ltd (trading as Celixir) | ||||||||||||||||||
Full Title: A Phase IIB, Randomised, Double-Blinded, Placebo-Controlled Study of the Efficacy and Safety of Intramyocardial Injection of Allogeneic Human Immunomodulatory Progenitor (iMP) cells in Patients Und... | ||||||||||||||||||
Medical condition: Ischaemic heart disease post MI | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001505-90 | Sponsor Protocol Number: 18CH049 | Start Date*: 2018-10-01 | ||||||||||||||||
Sponsor Name:CHU de Saint Etienne | ||||||||||||||||||
Full Title: Decolonization of patients carrying S. aureus before cardiac surgery: study of the risk factors associated with failure | ||||||||||||||||||
Medical condition: Decolonization of S. aureus nasal carriers before cardiac surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000135-40 | Sponsor Protocol Number: 260585 | Start Date*: 2016-05-12 | ||||||||||||||||||||||||||
Sponsor Name:Zealand University Hospital, Department of Surgery | ||||||||||||||||||||||||||||
Full Title: Endoscopic assisted electrochemotherapy in addition to neoadjuvant treatment of locally advanced rectal cancer: a randomized clinical phase II trial. | ||||||||||||||||||||||||||||
Medical condition: Locally advanced rectal cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002618-38 | Sponsor Protocol Number: AnesBar01 | Start Date*: 2013-10-15 | ||||||||||||||||
Sponsor Name: | ||||||||||||||||||
Full Title: Does preperitoneal local anesthesia in laparoscopic gastric bypass surgery reduce postoperative pain and opioid consumption? | ||||||||||||||||||
Medical condition: Postoperative pain | ||||||||||||||||||
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Population Age: Adults | 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: 2015-005090-20 | Sponsor Protocol Number: FADOI.01.2016 | Start Date*: 2018-05-17 | ||||||||||||||||
Sponsor Name:FONDAZIONE FADOI | ||||||||||||||||||
Full Title: Rivaroxaban or placebo for extended antithrombotic prophylaxis after laparoscopic surgery for colorectal cancer: a randomized, double blind, placebo-controlled study. THE PRO-LAPS STUDY II | ||||||||||||||||||
Medical condition: Prevention of venous thromboembolism after laparoscopic surgery for colorectal cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001027-33 | Sponsor Protocol Number: PAFIBAR1.0 | Start Date*: 2023-06-07 | |||||||||||
Sponsor Name:FIMABIS | |||||||||||||
Full Title: Evaluation of the effect of Opioid-Free Anesthesia on oxygenation in bariatric surgery | |||||||||||||
Medical condition: Bariatric surgery | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002217-19 | Sponsor Protocol Number: 232100-0024 | Start Date*: 2012-12-13 |
Sponsor Name:Dept of Surgery [...] | ||
Full Title: Postoperative treatment with Vitamin D for patients with a history of Bariatric Surgery in C and U County. | ||
Medical condition: Hypovitaminosis D after bariatric surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-015799-92 | Sponsor Protocol Number: FER-SURG02-Pilot | Start Date*: 2009-12-02 |
Sponsor Name:Universitätspital Zürich Anästhesie | ||
Full Title: Intravenous ferric carboxymaltose (Ferinject®) with or without Erythropoietin for the correction of preoperative anaemia in patients undergoing orthopaedic surgery | ||
Medical condition: • To evaluate the effect of the administration of ferric carboxymaltose (Ferinject®) with or without erythropoietin vs. no treatment (standard therapy) on the preoperative anaemia status in patient... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001487-23 | Sponsor Protocol Number: TPU-SL-EU05-02 | Start Date*: 2006-06-05 |
Sponsor Name:Teikoku Pharma USA, Inc. | ||
Full Title: A Double Blind Randomized Controlled Study of the Effiacy and Safety of Topical Sterile 5% Lidocaine Patch in the Treatment of Postoperative Pain Due to Plastic Surgery of the Breast | ||
Medical condition: Postoperative Pain Due to the Plastic Surgery of the Breast | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: LV (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2009-015086-31 | Sponsor Protocol Number: Ten03 | Start Date*: 2010-03-16 |
Sponsor Name:Bio Products Laboratory Limited | ||
Full Title: Ten03: A Phase III Open, Multicentre Study to Investigate the Safety and Efficacy of BPL’s High Purity Factor X in the treatment of the Factor X Deficient Subjects Undergoing Surgery | ||
Medical condition: Factor X Deficiency | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-012372-27 | Sponsor Protocol Number: 200901 | Start Date*: 2009-09-17 | |||||||||||
Sponsor Name:LUMC | |||||||||||||
Full Title: The Sevoflurane study, understanding the effects of Sevoflurane to improve safety and outcome of cardiac surgery | |||||||||||||
Medical condition: myocardial ischemia reperfusion injury during cardiac surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
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: 2014-004964-39 | Sponsor Protocol Number: 51503 | Start Date*: 2015-05-22 |
Sponsor Name:Sint Antonius Ziekenhuis | ||
Full Title: Clonidine as Additive for Locoregional Postoperative Analgesia in Foot and Anckle Surgery | ||
Medical condition: Postoperative pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001551-22 | Sponsor Protocol Number: RECIPE2014 | Start Date*: 2014-12-18 |
Sponsor Name:Charité Universitätsmedizin | ||
Full Title: Reduction of postoperative wound infections by antiseptica | ||
Medical condition: Laparotomy wound after closure of the fascia after visceral surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-000588-41 | Sponsor Protocol Number: TRANEX-URO | Start Date*: 2008-02-26 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: Tranexamic acid efficacy reducing surgery bleding in patients undergoing surgery for complete prostatectomy. | |||||||||||||
Medical condition: patients undergoing prostatic radical surgery for prostatic cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004506-21 | Sponsor Protocol Number: 21/2 | Start Date*: 2021-11-30 |
Sponsor Name:Hospital Universitario Fundación Alcorcón | ||
Full Title: ERECTOR SPINAE PLANE CATHETERS IN SCOLIOSIS SURGERY | ||
Medical condition: Postoperative pain following scoliosis surgery | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001944-13 | Sponsor Protocol Number: ZAA15CPP | Start Date*: 2016-07-27 |
Sponsor Name:Zaans Medisch Centrum | ||
Full Title: Chloroprocaine vs prilocaine for spinal anaesthesia in day-case surgery: a double-blind randomized trial | ||
Medical condition: Patients scheduled for ambulatory knee arthroscopy surgery receive one of the two spinal anaesthetics | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-005452-11 | Sponsor Protocol Number: - | Start Date*: 2022-01-21 |
Sponsor Name:Medizinische Universität Innsbruck | ||
Full Title: Influence of the PECS II block on postoperative pain and opioid demand in patients undergoing minimal invasive cardiac surgery | ||
Medical condition: Patients scheduled for minimal invasive cardia surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
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