- Trials with a EudraCT protocol (5,757)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (321)
5,757 result(s) found for: Surgery.
Displaying page 1 of 288.
EudraCT Number: 2018-001457-28 | Sponsor Protocol Number: PI2018_843_0020 | Start Date*: Information not available in EudraCT |
Sponsor Name:CHU Amiens-Picardie | ||
Full Title: Analgesic contribution of the suprazygomatic maxillary nerve block after cleft palate surgery in children | ||
Medical condition: cleft palate repair surgery with or without upper lip surgery | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001167-22 | Sponsor Protocol Number: 43488 | Start Date*: 2017-06-29 |
Sponsor Name: | ||
Full Title: Spinal Morphine in laparoscopic gastro-intestinal surgery | ||
Medical condition: Patients with indications for laparoscopic gastro-intestinal surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004804-21 | Sponsor Protocol Number: ANST_PREVENT | Start Date*: 2020-01-13 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: A Randomized, Double-blind, Placebo-controlled Trial on the Prevention of Chronic Postoperative Pain after Inguinal Hernia and Knee Surgery by Postoperative Treatment with Tapentadol. | ||
Medical condition: Chronic pain after inguinal hernia surgery and knee replacement surgery. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004561-34 | Sponsor Protocol Number: 4.2006.1285 | Start Date*: 2006-11-16 |
Sponsor Name:St. Olavs Hospital | ||
Full Title: Tranexamic acid to elderly patients undergoing combined AVR and CABG surgery. | ||
Medical condition: We will investigate whether tranexamic acid given as a bolus injection at the start of surgery followed by a continuous infusion during surgery reduces postoperative bleeding in patients above 70 y... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NO (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004878-26 | Sponsor Protocol Number: 26842468452 | Start Date*: 2013-02-07 |
Sponsor Name:Karolinska University Hospital Solna | ||
Full Title: Antibiotic prophylaxis in patients undergoing primary or secondary breast reconstruction with implants, a randomized parallel two armed prospective clinical trial. | ||
Medical condition: The incidence of postoperative infections in patients with breast cancer or a history of breast cancer, after elective surgery with primary or secondary first-time breast reconstruction with implan... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Prohibited by CA) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001443-31 | Sponsor Protocol Number: 1801 | Start Date*: 2018-11-21 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: DOAC Levels prior to Incision study: DALI study | ||
Medical condition: No medical condition will be investigated. This study will only investigate DOAC levels during surgery. Patients who use DOACs are patients with venous thrombosis and atrial fibrillation. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
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: 2013-004750-24 | Sponsor Protocol Number: 2013003 | Start Date*: 2014-03-17 | |||||||||||
Sponsor Name:Rode Kruis Ziekenhuis | |||||||||||||
Full Title: Omega-3 fatty acids in bariatric gastric bypass surgery: effects on liver volume, immune response and erythrocyte function | |||||||||||||
Medical condition: Patients qualified for bariatric surgery | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005347-79 | Sponsor Protocol Number: UMCN-AKF-21.07 | Start Date*: 2022-03-31 | ||||||||||||||||
Sponsor Name:Radboud University Medical Center | ||||||||||||||||||
Full Title: The influence of having bariatric surgery on the pharmacokinetics, safety and efficacy of the novel non-nucleoside reverse transcriptase inhibitor doravirine (LABRADOR) | ||||||||||||||||||
Medical condition: HIV plus bariatric surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000956-16 | Sponsor Protocol Number: 43907 | Start Date*: 2013-07-15 |
Sponsor Name:Erasmus Medical Center | ||
Full Title: Effect of low-dose ketamine on postoperative delirium in patients undergoing noncardiac surgery: a pilot study. | ||
Medical condition: To investigate the clinical use of Ketamine for the prevention of postoperative delirium in patients undergoing noncardiac surgery. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002222-70 | Sponsor Protocol Number: Lidobreast | Start Date*: 2013-11-15 |
Sponsor Name:University Medical Centre St Radboud | ||
Full Title: Pilot study: Targeting the inflammatory response after breast cancer surgery with lidocaïne and dexamethasone | ||
Medical condition: Breast cancer patients who undergo surgery for treatment. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004711-39 | Sponsor Protocol Number: 2017-11-10 | Start Date*: 2018-04-10 | |||||||||||
Sponsor Name:Merja Kokki | |||||||||||||
Full Title: Tramadol-paracetamol in spine surgery | |||||||||||||
Medical condition: Postoperative pain after spine surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000263-92 | Sponsor Protocol Number: 17-251 | Start Date*: 2018-05-28 | |||||||||||
Sponsor Name:CHU CAEN | |||||||||||||
Full Title: Spironolactone and perioperative atrial fibrillation occurrence in cardiac surgery patients: a multicenter randomized, double-blind study | |||||||||||||
Medical condition: Patients > 18 years referred for elective cardiac bypass graft (CABG) surgery ± aortic valve replacement (AVR) without any systolic heart failure or any mitral surgery associated | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2012-002816-19 | Sponsor Protocol Number: Frax001 | Start Date*: 2012-10-25 |
Sponsor Name:Rijnstate Hospital | ||
Full Title: Prospective, pharmacokinetic study for determination of the relationship between lean body weight and anti-Xa activity 4 hours after subcutaneous injection of 5700 IU nadroparin in morbidly obese p... | ||
Medical condition: patients; perioperative in bariatric surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000818-78 | Sponsor Protocol Number: 7-010-MR | Start Date*: 2008-09-25 | |||||||||||
Sponsor Name:POLICLINICO SAN DONATO IRCSS | |||||||||||||
Full Title: Efficacy of fenoldopam mesilate in controlling splanchnic ischemia during cardiopulmonary bypass | |||||||||||||
Medical condition: Patients to be submitted to cardiac surgery with expected prolonged CPB time | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004607-39 | Sponsor Protocol Number: 2013-00460739 | Start Date*: 2014-04-11 |
Sponsor Name:CUB Hopital Erasme | ||
Full Title: Safety of preoperative administration of hemin to reduce the risk of acute kidney injury after on-pump cardiac surgery: a pilot randomised study in double blind. | ||
Medical condition: Acute kidney injury which is associated with on-pump cardiac surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001756-19 | Sponsor Protocol Number: MTP-2019-01 | Start Date*: 2019-12-11 |
Sponsor Name:María de los Ángeles Tena Pajuelo (Investigador independiente) | ||
Full Title: MULTI-CENTER, DOUBLE-BLIND, CONTROLLED, PARALLEL AND RANDOMIZED STUDY TO COMPARE THE EFFECTIVENESS OF 0.1 ΜG / KG / MIN OF LEVOSIMENDAN VERSUS PLACEBO IN THE POSTOPERATIVE OF CARDIAC PROGRAMMED SUR... | ||
Medical condition: Patients who have preoperatively severe left ventricular dysfunction (LVEF ≤ 35%) and will be scheuled for cardiac surgery on cardiopulmonary bypass. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-008354-23 | Sponsor Protocol Number: ECAL-CCPB-08-07 | Start Date*: 2009-04-30 |
Sponsor Name:Cubist Pharmaceuticals,INC | ||
Full Title: CONSERVTM – 2 (Clinical Outcomes and Safety Trial to Investigate Ecallantide’s Effect on Reducing Surgical Blood Loss Volume) – A Phase 2 Randomized Double-Blind Active-Controlled Study in Subjects... | ||
Medical condition: Reduction of blood loss in subjects exposed to CPB during cardiac surgery at high risk for bleeding | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PL (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-002325-28 | Sponsor Protocol Number: D-PLEX311 | Start Date*: 2020-09-23 | |||||||||||
Sponsor Name:PolyPid Ltd. | |||||||||||||
Full Title: Phase III, Prospective, Multinational, Multicenter, Randomized, Controlled, Two‐arm, Double Blind Study to assess Efficacy and Safety of D‐PLEX Administered Concomitantly with the Standard of Care ... | |||||||||||||
Medical condition: Prevention of post abdominal surgery incisional infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) CZ (Completed) HR (Completed) HU (Completed) SK (Completed) PL (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
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