- Trials with a EudraCT protocol (101)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
101 result(s) found for: Perioperative mortality.
Displaying page 1 of 6.
EudraCT Number: 2004-005136-76 | Sponsor Protocol Number: ASINC101C | Start Date*: 2005-05-02 |
Sponsor Name:Professor Christina Eintrei,Institution of Medical & Health, Section of Anesthesiology | ||
Full Title: Aspirin in noncardiac surgery | ||
Medical condition: Patients with cardiovascular risk factors undergoing elective non-cardiac surgery of high or intermediate risk. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001479-22 | Sponsor Protocol Number: NCT03021525 | Start Date*: 2017-08-04 |
Sponsor Name:University Medical Center Hamburg-Eppendorf, Germany | ||
Full Title: Individualized perioperative hemodynamic goal-directed therapy in major abdominal surgery (iPEGASUS-trial) | ||
Medical condition: - Hemodynamic Instability - Cardiac Output - High Peroperative Complication | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003088-76 | Sponsor Protocol Number: 11-170 | Start Date*: 2014-07-14 |
Sponsor Name:Clinical Evaluation Research Unit (CERU) | ||
Full Title: SodiUm SeleniTe Adminstration IN Cardiac Surgery surgery (SUSTAIN CSX®-trial) - A randomized controlled trial of high dose sodium-selenite administration in high risk cardiac surgical patients | ||
Medical condition: Selenium is a key component of a number of selenoproteins which protect against oxidative stress and is well recognised for its prominent role in immune defence. Selenoproteins have the potential t... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001561-28 | Sponsor Protocol Number: HES08 | Start Date*: 2008-07-21 |
Sponsor Name:Klinik für Anästhesiologie und Operative Intensivmedizin Klinikum Ludwigshafen | ||
Full Title: Influence of perioperative HES 130/04 adminstration on postoperative complications: A prospective randomized trial in patients undergoing colorectal surgery. | ||
Medical condition: Adult patients (>18 years) of both gender undergoing elective colorectal surgery (hemicolectomy left/right, sigmoid colectomy, rectal resection/amputation) without concomitant resection of liver me... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001710-32 | Sponsor Protocol Number: 2006-101 | Start Date*: 2006-07-05 |
Sponsor Name:Dept. of Anaesthesia, Centre of Head and Orthopaedics, Copenhagen University Hospital Rigshospitalet | ||
Full Title: PeRioperative OXygen fraction – effect on surgical site Infection and pulmonary complications after abdominal surgery. (The PROXI-study) | ||
Medical condition: Laparotomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-022417-25 | Sponsor Protocol Number: NL 33608 | Start Date*: 2011-04-18 | |||||||||||
Sponsor Name:University Medical Center Groningen | |||||||||||||
Full Title: Pheochromocytoma RandomisEd Study Comparing adRenoreceptor Inhibiting agents for Preoperative Treatment | |||||||||||||
Medical condition: Perioperative hemodynamic control in patients undergoing resection of a pheochromocytoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003595-11 | Sponsor Protocol Number: 2004-06-DP-119-RKF-25 | Start Date*: 2005-03-18 |
Sponsor Name:Canadian Cardiovascular Collaboration, Population Health Research Institute, McMaster University | ||
Full Title: PeriOperative ISchemic Evaluation study | ||
Medical condition: Perioperative cardiac events frequently complicate non-cardiac surgery resulting in significant morbidity, mortality and cost. There is no clear evidence from RCTs on how to lower perioperative ca... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-005559-34 | Sponsor Protocol Number: AIO-PAK-0313 | Start Date*: 2015-01-19 | |||||||||||
Sponsor Name:AIO-Studien-gGmbH | |||||||||||||
Full Title: Neoadjuvant plus adjuvant or only adjuvant nab-Paclitaxel plus Gemcitabine for resectable pancreatic cancer - The AIO-NEONAX trial (AIO-PAK-0313) A prospective, randomized, controlled, phase II st... | |||||||||||||
Medical condition: Resectable pancreatic cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003836-35 | Sponsor Protocol Number: 2017-001-COPAF | Start Date*: 2018-08-17 | ||||||||||||||||
Sponsor Name:Population Health Research Institute | ||||||||||||||||||
Full Title: Colchicine For The Prevention Of Perioperative Atrial Fibrillation In Patients Undergoing Thoracic Surgery (COP-AF) | ||||||||||||||||||
Medical condition: Perioperative atrial fibrillation / atrial flutter after thoracic surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) BE (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-000442-21 | Sponsor Protocol Number: RC17_0029 | Start Date*: 2017-09-12 | |||||||||||
Sponsor Name:CHU de Nantes | |||||||||||||
Full Title: Effects of perioperative administration of dexamethasone on postoperative complications and mortality after non-cardiac major surgery : a randomized, multicentre, double blind, study | |||||||||||||
Medical condition: non-cardiac major surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000591-34 | Sponsor Protocol Number: 123456 | Start Date*: 2011-05-06 |
Sponsor Name:Mater University Hospital | ||
Full Title: SIRS Steroids In caRdiac Surgery Trial | ||
Medical condition: Study Objective(s) To determine whether high-risk patients undergoing cardiac surgery requiring CPB derive benefit from perioperative steroids. Study Design Multicentre, International, random... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001673-32 | Sponsor Protocol Number: P150915 | Start Date*: 2016-10-19 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: PREVENTION OF POSTOPERATIVE PANCREATIC FISTULA BY SOMATOSTATIN (PREFIPS) | |||||||||||||
Medical condition: Patients candidate for pancreatic surgery (pancreaticoduodenectomy or distal pancreatectomy with or without splenectomy). | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000265-20 | Sponsor Protocol Number: LM02 | Start Date*: 2012-06-06 |
Sponsor Name:ABCSG (Austrian Breast & Colorectal Cancer Study Group) | ||
Full Title: A perioperative, single-arm multicenter Phase II academic trial to investigate the efficacy and safety of panitumumab in combination with irinotecan/5-fluorouracil/leucovorin (FOLFIRI) in patients ... | ||
Medical condition: previously untreated, wild-type RAS, potentially resectable colorectal cancer liver metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-003173-28 | Sponsor Protocol Number: 11112 | Start Date*: 2012-06-13 |
Sponsor Name:Helsinki University Hospital | ||
Full Title: Volume replacement therapy in cardiac surgery: effect on renal function. | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005206-31 | Sponsor Protocol Number: 2006-09 | Start Date*: 2007-01-25 |
Sponsor Name:Örebro University Hospital | ||
Full Title: Perioperative Morbidity in Elderly patients undergoing Surgery for Fracture Neck of Femur. The Effect of Plasma or Ocplex® for reversal of Warfarin anticoagulation. | ||
Medical condition: Patients undergoing surgery for the repair of fracture neck of femur that are on chronic oral warfarin sodium as anticoagulation prophylactics. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002634-20 | Sponsor Protocol Number: NBF_HK_01_2018 | Start Date*: 2018-10-23 | ||||||||||||||||
Sponsor Name:Anaesthesia Department, Hvidovre Hospital, Capital Region of Denmark | ||||||||||||||||||
Full Title: Highdose steroid for total knee arthroplasty - A randomized doubleblindet controlled trial. | ||||||||||||||||||
Medical condition: Perioperative management of total knee-arthroplasty because of knee-osteoarthritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002636-25 | Sponsor Protocol Number: NBF_HK_03_2018 | Start Date*: 2018-10-23 | |||||||||||||||||||||
Sponsor Name:Anaesthesia Department, Hvidovre Hospital, Capital Region of Denmark. | |||||||||||||||||||||||
Full Title: Highdose Steroid for High Pain Responders undergoing Total Hip-arthroplasty - A randomized doubleblindet controlled trial. | |||||||||||||||||||||||
Medical condition: Perioperative management of total hip-arthroplasty because of hip-osteoarthritis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-018754-13 | Sponsor Protocol Number: FLOT4 | Start Date*: Information not available in EudraCT |
Sponsor Name:Krankenhaus Nordwest GmbH | ||
Full Title: A randomized multicenter Phase II/III Study comparing 5-FU, Leucovorin, Oxaliplatin and Docetaxel (FLOT) versus Epirubicin, Cisplatin and 5-FU (ECF) in patients with locally advanced resectable ad... | ||
Medical condition: locally advanced resectable adenocarcinoma of the esophagogastreal junction or the stomach | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003670-14 | Sponsor Protocol Number: NA | Start Date*: 2018-01-11 |
Sponsor Name:University Hospital Limerick | ||
Full Title: The role of selective decontamination of the digestive tract in preventing surgical site infections in elective colorectal resections: a randomized controlled trial (SELDDEC Trial) | ||
Medical condition: Surgical Site Infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017137-22 | Sponsor Protocol Number: 190178 | Start Date*: 2013-04-16 |
Sponsor Name:Klinische Abteilung für Thorax -u. Hyperbare Chirurgie, Medizinische Universität Graz | ||
Full Title: Clinical course after substitution of Vitamin-D deficiency in patients with lung cancer or oesophageal carcinoma. Double blind randomised prospective, placebo-controlled study. | ||
Medical condition: Patients admitted for treatment on a general thoracic surgery division with the following conditions: Lung cancer Esophageal cancer Cancer of the gastroesophageal junction (GEJ) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
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