- 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 4 of 6.
EudraCT Number: 2021-004411-11 | Sponsor Protocol Number: NeoTreme | Start Date*: 2023-05-03 | |||||||||||
Sponsor Name: University Hospital Schleswig-Holstein, Campus Lübeck | |||||||||||||
Full Title: Phase 2 Study of Preoperative Gemcitabine Plus Cisplatin with Durvalumab (MEDI4736) and Tremelimumab in intrahepatic cholangiocarcinoma (NeoTreme) | |||||||||||||
Medical condition: Intrahepatic cholangiocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003217-11 | Sponsor Protocol Number: NL82304.058.22 | Start Date*: 2023-02-24 | |||||||||||||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||||||||||||
Full Title: Standard versus Pre-emptive Antibiotic Treatment to Reduce the Rate of Infectious Outcomes after Whipple procedure (SPARROW): a multicenter, randomized controlled trial | |||||||||||||||||||||||
Medical condition: Pancreatic head malignancy | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-005015-13 | Sponsor Protocol Number: C0947 | Start Date*: 2018-05-18 | |||||||||||
Sponsor Name:The Clatterbridge Cancer Centre NHS Foundation Trust | |||||||||||||
Full Title: NICO - CA209-891: Neoadjuvant and adjuvant nivolumab as Immune Checkpoint inhibition in Oral cavity cancer | |||||||||||||
Medical condition: Locally advanced squamous cell carcinoma of the oral cavity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002461-35 | Sponsor Protocol Number: PREBOTPilot | Start Date*: 2019-12-06 | |||||||||||
Sponsor Name:Ruprecht-Karls-University Heidelberg Medical Faculty represented by Universitätsklinikum Heidelberg and its acting Comm | |||||||||||||
Full Title: Monocenter, randomized, controlled, open-label, phase-II clinical trial of PREoperative endoscopic injection of BOTulinum toxin in the sphincter of Oddi to reduce postoperative pancreatic fistula a... | |||||||||||||
Medical condition: Elective distal pancreatectomy for any underlying disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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: 2009-011623-31 | Sponsor Protocol Number: AGO/2009/003 | Start Date*: 2009-04-24 |
Sponsor Name:University Hospital Ghent | ||
Full Title: Individually adapted immunosuppression in de novo renal transplantation based on immune function monitoring: a prospective randomised study Extension study: The impact of magnesium supplementation ... | ||
Medical condition: de novo renal transplantation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000401-76 | Sponsor Protocol Number: 7715 | Start Date*: 2019-11-26 |
Sponsor Name:University hospital of Montpellier | ||
Full Title: Transfusion savings in heart surgery: impact of individual strategy, optimized by erythropoietin (EPO) and metabolic adjustment (ScvO2) | ||
Medical condition: Heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
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: 2017-004596-31 | Sponsor Protocol Number: NL62772 | Start Date*: 2019-03-25 | ||||||||||||||||
Sponsor Name:UMC Utrecht | ||||||||||||||||||
Full Title: CeRebrUm and CardIac protection with Allopurinol in neonates with critical congenital heart disease requiring cardiac surgery with cardiopulmonary bypass | ||||||||||||||||||
Medical condition: Brain injury in neonates with critical congenital heart disease requiring cardiac surgery with cardiopulmonary bypass. | ||||||||||||||||||
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Population Age: Newborns, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015865-30 | Sponsor Protocol Number: PAHFRAC-01 | Start Date*: 2010-06-24 | |||||||||||
Sponsor Name:Máximo Bernabeu Wittel | |||||||||||||
Full Title: ENSAYO CLINICO RANDOMIZADO DOBLE CIEGO DE HIERRO CARBOXIMALTOSA INTRAVENOSO CON O SIN ERITOPOYETINA PARA LA PREVENCIÓN DE TRANSFUSIONES DE CONCENTRADOS DE HEMATÍES EN EL PERIOPERATORIO DE FRACTURA ... | |||||||||||||
Medical condition: Pacientes adultos ingresados en el Hospital por fractura de cadera osteoporótica. Adult patients admitted in Hospital for osteoporotic hip fracture | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004505-29 | Sponsor Protocol Number: 2676 | Start Date*: 2008-05-15 | |||||||||||
Sponsor Name:Royal Marsden NHS Trust | |||||||||||||
Full Title: Phase II clinical trial of capecitabine and oxaliplatin plus bevacizumab as neoadjuvant treatment for patients with previously untreated unresectable liver-only metastases from colorectal cancer | |||||||||||||
Medical condition: Metastatic colorectal adenocarcinoma with metastases involving the liver only | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001507-13 | Sponsor Protocol Number: AIO-STO-0310 | Start Date*: 2011-10-24 | ||||||||||||||||
Sponsor Name:AIO-Studien-gGmbH | ||||||||||||||||||
Full Title: Multicenter, explorative phase II study of perioperative 5-FU, leucovorin, docetaxel, and oxaliplatin (FLOT) in combination with Trastuzumab in patients with HER2-positive, locally advanced resecta... | ||||||||||||||||||
Medical condition: HER2-positive, locally advanced, resectable adenocarcinoma of the gastroesophageal junction or stomch | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000823-24 | Sponsor Protocol Number: P-HIPEC | Start Date*: 2017-02-14 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA DI MODENA | ||||||||||||||||||
Full Title: P-HIPEC CYTOREDUCTION PLUS HIPEC IN PATIENTS AFFECTED BY PERITONEAL CARCINOMATOSIS: A FEASIBILITY TRIAL | ||||||||||||||||||
Medical condition: peritoneal carcinomatosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-005144-14 | Sponsor Protocol Number: 01-CARDIONIDO | Start Date*: 2018-04-12 |
Sponsor Name:Dr. Forteza Gil | ||
Full Title: Comparative study of two types of cardioplegia during cardiac surgery in the adult patient | ||
Medical condition: Cardiac surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-005282-39 | Sponsor Protocol Number: AIRC-2013-144445 | Start Date*: 2014-05-22 | ||||||||||||||||
Sponsor Name:Fondazione IRCCS Istituto Nazionale dei Tumori di Milano | ||||||||||||||||||
Full Title: Effects of high Intra-abdominal pressure on tissue diffusion and pharmacokinectics of cisplatin during HIPEC | ||||||||||||||||||
Medical condition: patients affected by peritoneal carcinomatosis from colorectal cancer or pseudomyxoma peritonei | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007798-18 | Sponsor Protocol Number: AIO/CAO-STO-0801 | Start Date*: 2010-07-01 | ||||||||||||||||
Sponsor Name:AIO-Studien-gGmbH | ||||||||||||||||||
Full Title: An Open Label Randomized Controlled Phase II Trial of Panitumumab in Combination with Epirubicin, Cisplatin and Capecitabine (ECX) versus ECX Chemotherapy alone in Subjects with Locally Advanced Ga... | ||||||||||||||||||
Medical condition: Subjects with Locally Advanced Gastric Cancer or Cancer of the Gastroesophageal Junction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-000383-28 | Sponsor Protocol Number: CA224-050 | Start Date*: 2019-05-23 | |||||||||||||||||||||
Sponsor Name:University Hospital Essen | |||||||||||||||||||||||
Full Title: Perioperative immunotherapy vs. chemo-immunotherapy stratified by early response evaluation in patients with advanced gastric cancer (GC) and adenocarcinoma of the esophago-gastric junction (AEG) (... | |||||||||||||||||||||||
Medical condition: Histologically confirmed, resectable advanced gastric cancer GC and adenocarcinoma of the esophago-gastric junction | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006301-10 | Sponsor Protocol Number: MAGNA | Start Date*: 2012-05-10 | ||||||||||||||||
Sponsor Name:Fundació Clinic per a la Recerca Biomèdica | ||||||||||||||||||
Full Title: Perioperative Magnesium Sulphate as a cerebral protector in neurosurgical patients | ||||||||||||||||||
Medical condition: Patient who are going to be under cerebral parenchyma resection, due to epilepsy or tumor | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005736-17 | Sponsor Protocol Number: NL56697.041.16 | Start Date*: 2016-09-20 | ||||||||||||||||||||||||||
Sponsor Name:University Medical Center Utrecht | ||||||||||||||||||||||||||||
Full Title: Prevention of severe infectious complications after colorectal surgery using antimicrobial decontamination of the digestive tract (PreCaution trial) | ||||||||||||||||||||||||||||
Medical condition: The medical condition under investigation: surgical site infections (bacterial) after elective colorectal surgery. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004707-38 | Sponsor Protocol Number: CCR 3065 | Start Date*: 2005-04-08 | |||||||||||
Sponsor Name:Royal Marsden NHS Trust | |||||||||||||
Full Title: A multicentre randomised phase II clinical trial comparing oxaliplatin (Eloxatin), capecitabine (Xeloda) and pre-operative radiotherapy with or without cetuximab followed by total mesorectal excisi... | |||||||||||||
Medical condition: High risk operable rectal adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Ongoing) SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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