- Trials with a EudraCT protocol (15)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
15 result(s) found for: Bowel infarction.
Displaying page 1 of 1.
EudraCT Number: 2009-015013-46 | Sponsor Protocol Number: AnaesthesiaResearch024 | Start Date*: 2009-12-14 |
Sponsor Name:Alfred Health | ||
Full Title: The ATACAS Trial: Aspirin and Tranexamic Acid for Coronary Artery Surgery Trial | ||
Medical condition: Coronary Artery Bypass Grafting | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004840-30 | Sponsor Protocol Number: PrepDial | Start Date*: 2020-11-04 | |||||||||||
Sponsor Name:Policlinico di Bari-UO Gastroenterologia | |||||||||||||
Full Title: Comparison of low-volume versus high-volume polyethylene glycol based bowel preparation for colonoscopy in people receiving hemodialysis: a randomized non-inferiority trial. | |||||||||||||
Medical condition: Colonoscopy in people receiving hemodialysis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000117-34 | Sponsor Protocol Number: Nordic VII | Start Date*: 2005-04-22 |
Sponsor Name:The Nordic Colorectal Cancer Biomodulation Group | ||
Full Title: Combination of 5-Fluorouracil/Folinate/Oxaliplatin (Eloxatin®) (FLOX regimen) with Concomitant or Concomitant and Maintenance Administration of Cetuximab (Erbitux®), in First-Line Treatment of Meta... | ||
Medical condition: Patient with metastatic colorectal cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) IS (Completed) FI (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-005112-15 | Sponsor Protocol Number: TARTARE-2S-01 | Start Date*: 2016-09-29 | |||||||||||
Sponsor Name:Inselspital, Universitätspital Bern | |||||||||||||
Full Title: TARGETED TISSUE PERFUSION VERSUS MACROCIRCULATORY-GUIDED STANDARD CARE IN PATIENTS WITH SEPTIC SHOCK (TARTARE-2S) | |||||||||||||
Medical condition: Critically ill adult patients with septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003666-17 | Sponsor Protocol Number: CS/2007/2608 | Start Date*: 2007-11-09 | |||||||||||
Sponsor Name:University Hospitals Bristol NHS Foundation Trust | |||||||||||||
Full Title: The ATACAS Trial: Aspirin and Tranexamic Acid for Coronary Artery Surgery Trial | |||||||||||||
Medical condition: Ischamic heart disease operated | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004133-16 | Sponsor Protocol Number: IH141 | Start Date*: 2015-02-19 |
Sponsor Name:Hull and east Yorkshire Hospitals Trust | ||
Full Title: Exploratory multicentre prospective double blinded randomised controlled pilot study of the effect of intravenous iron supplementation(Monofer)in iron deficient but not anaemic patients with Chroni... | ||
Medical condition: Chronic Kidney Disease stages 3b to 5 with iron deficiency | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-004636-25 | Sponsor Protocol Number: ACOTAS_G098 | Start Date*: 2021-06-17 | ||||||||||||||||
Sponsor Name:GERCOR | ||||||||||||||||||
Full Title: A phase II study to evaluate the rate of cardiovascular events during trifluridine/tipiracil +/-oxaliplatin treatment in colorectal/oesogastric adenocarcinoma patients that have experienced a pas... | ||||||||||||||||||
Medical condition: colorectal or oesogastric adenocarcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001506-29 | Sponsor Protocol Number: ML 18729 | Start Date*: 2005-10-10 | |||||||||||
Sponsor Name:Group of Clinical Investigation in Radiotherapy Oncology (GICOR) | |||||||||||||
Full Title: PHASE I/II TRIAL OF ERLOTINIB, RADIATIONTHERAPY, AND CISPLATIN IN PATIENTS WITH COMPLETE RESECTED SQUAMOUS CELL CARCINOMA OF THE HEAD AND NECK Ensayo Fase I/II de Erlotinib en combinación con radio... | |||||||||||||
Medical condition: PATIENTS WITH COMPLETE RESECTED SQUAMOUS CELL CARCINOMA OF THE HEAD AND NECK | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004333-34 | Sponsor Protocol Number: EORTC 55041 | Start Date*: 2005-09-20 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: A randomized, multicentre, phase III study of Erlotinib versus observation in patients with no evidence of disease progression after first line, platinum-based chemotherapy for high-risk Stage I an... | |||||||||||||
Medical condition: Histologically confirmed high-risk FIGO stage I (grade 3, or aneuploid grade 1 or 2, or clear cell), or Stages II-IV ovarian epithelial, primary peritoneal, and fallopian tube cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) IT (Completed) AT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001078-34 | Sponsor Protocol Number: 07-09-04/07 | Start Date*: 2008-09-29 | ||||||||||||||||
Sponsor Name:Maastro Clinic | ||||||||||||||||||
Full Title: Phase I/II study for patients with newly diagnosed glioblastoma testing nelfinavir in combination with radiotherapy and concomitant and adjuvant temozolomide | ||||||||||||||||||
Medical condition: Phase I/II study for patients with newly diagnosed glioblastoma testing nelfinavir in combination with radiotherapy and concomitant and adjuvant temozolomide | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001529-15 | Sponsor Protocol Number: RATIOSTUDY | Start Date*: 2016-10-26 | |||||||||||
Sponsor Name:AZIENDA SOCIO-SANITARIA TERRITORIALE DI LECCO (ASST LECCO) | |||||||||||||
Full Title: Randomized Anticoagulation Trial In Opcab HIGH DOSE VERSUS LOW DOSE HEPARINIZATION IN PATIENTS | |||||||||||||
Medical condition: Off-pump coronary artery bypass grafting (OPCAB) is an established alternative to on-pump coronary artery bypass grafting (CABG), OPCAB, like any other surgical procedure, determines a pro-coagulan... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003998-96 | Sponsor Protocol Number: AXAGIST | Start Date*: 2019-04-03 | |||||||||||
Sponsor Name:Centrum Onkologii – Instytut im. Marii Skłodowskiej - Curie | |||||||||||||
Full Title: A Phase II, single arm Study of avelumab In combination with Axitinib in Patients With unresectable/metastatic Gastrointestinal Stromal Tumor after failure of standard therapy - AXAGIST | |||||||||||||
Medical condition: GIST - unresectable/metastatic Gastrointestinal Stromal Tumor after failure of standard therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006532-21 | Sponsor Protocol Number: 40054-22062 | Start Date*: 2008-10-27 | ||||||||||||||||
Sponsor Name:EORTC | ||||||||||||||||||
Full Title: Preoperative chemoradiotherapy and postoperative chemotherapy with capecitabine and oxaliplatin vs. capecitabine alone in locally advanced rectal cancer (PETACC-6) | ||||||||||||||||||
Medical condition: locally advanced rectal cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) GB (Completed) FR (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-002588-23 | Sponsor Protocol Number: 2019/0407/HP | Start Date*: 2023-03-13 | ||||||||||||||||
Sponsor Name:CHU de Rouen | ||||||||||||||||||
Full Title: Neoadjuvant Chemotherapy for Obstructive Colon cancER first Treated by cOlostomy: A randomized phase III trial - COnCERTO (French 01-18) | ||||||||||||||||||
Medical condition: Patients first treated by stoma and requiring chemotherapy for obstructive colon cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001341-14 | Sponsor Protocol Number: BAY 59-7939 / 11527 | Start Date*: 2004-11-04 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Controlled, Double-Blind, Randomized, Dose-ranging Study of once-daily regimen of BAY59-7939 in the Prevention of VTE in Patients Undergoing Elective Total Hip Replacement-ODIXaHIP-OD Study | |||||||||||||
Medical condition: Deep Venous Thrombosis prophylaxis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) AT (Completed) ES (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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