- Trials with a EudraCT protocol (32)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5)
32 result(s) found for: Cefazolin.
Displaying page 1 of 2.
EudraCT Number: 2020-003174-50 | Sponsor Protocol Number: ALBUCEF | Start Date*: 2021-01-28 |
Sponsor Name:Medical University of Vienna Department of Cardiac Thoracic Vascular Anesthesia and Intensive Care Medicine | ||
Full Title: The Effect of Albumin Levels on Pharmacokinetics of Cefazolin in Adult Cardiac Surgery: A Prospective, Randomized, Open-label, Parallel-group Pharmacokinetic Study | ||
Medical condition: effect of hypoalbuminemia on pharmacokinetics of cefazolin | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000934-77 | Sponsor Protocol Number: 4.0 | Start Date*: 2018-05-11 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Target attainment of Cefazolin Continuous Infusion for Antibiotic Prophylaxis in patients undergoing CABG surgery | ||
Medical condition: Patients referred for CABG to the Department of Cardiac Surgery with planned isolated left mammary artery and vein/radial artery grafts preparation will be asked to participate in this trial. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002756-21 | Sponsor Protocol Number: 1663/2020 | Start Date*: 2021-02-23 |
Sponsor Name:Department of Cardiothoracic Anesthesia and Intensive Care Medicine, Medical University of Vienna | ||
Full Title: Plasma Pharmacokinetics of Prophylactic Cefazolin Administered for Cardiac Surgery: Comparison of Cardiopulmonary Bypass Priming with Additive Human Albumin 20% vs.Pure Crystalloid Priming: A singl... | ||
Medical condition: This is a pharmacokinetic trial for patients undergoing cardiac surgery. It will be investigated whether cardiopulmonary bypass priming substituted with human albumin 20% has an effect on the pharm... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002278-33 | Sponsor Protocol Number: PK_AB_NICU | Start Date*: 2018-09-27 |
Sponsor Name:Department of Clinical Pharmacology/Medical University of Vienna | ||
Full Title: Pharmacokinetics of antibiotics in cerebrospinal fluid of children with external ventricular drain | ||
Medical condition: We will obtain pharmacokinetic data of cefuroxime, vancomycin, gentamicin, ampicillin, linezolid, piperacillin/tazobactam and cefazolin in cerebrospinal fluid and plasma of children with external v... | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000998-68 | Sponsor Protocol Number: 1.0 | Start Date*: 2013-07-02 | ||||||||||||||||
Sponsor Name:Medizinische Universität Wien, Abteilung für Anästhesie und Intensivmedizin | ||||||||||||||||||
Full Title: Advanced antibiotic prophylaxis for optimal perioperative protection during coronary artery bypass grafting | ||||||||||||||||||
Medical condition: antibiotic prophylaxis during cardiac surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-005159-32 | Sponsor Protocol Number: A5951105 | Start Date*: 2005-04-28 | |||||||||||
Sponsor Name:Pfizer Limited | |||||||||||||
Full Title: Linezolid vs Vancomycin/Cefazolin in the treatment of hemodialysis patients with catheter-related gram-positive bloodstream infections | |||||||||||||
Medical condition: Catheter-related Gram-positive bloodstream infections. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) DE (Prematurely Ended) IT (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002396-34 | Sponsor Protocol Number: APHP180605 | Start Date*: 2019-12-23 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (APHP) | |||||||||||||
Full Title: Antibioprophylaxis for excision-graft surgery in burn patient: a multicenter randomized double-blind study | |||||||||||||
Medical condition: excision-graft surgery in burn patient with a TBSA% between 5% and 40% | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002438-35 | Sponsor Protocol Number: 860 | Start Date*: 2019-09-16 | ||||||||||||||||||||||||||
Sponsor Name:Radboudumc [...] | ||||||||||||||||||||||||||||
Full Title: Multiple doses versus single dose of cefazolin to prevent periprosthetic joint infection after revision arthroplasty: a multicenter open-label, randomized clinical trial. | ||||||||||||||||||||||||||||
Medical condition: Prevention of periprosthetic joint infection on patients undergoing revision surgery of the hip or knee. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016532-12 | Sponsor Protocol Number: Version1.0 | Start Date*: 2009-12-28 | ||||||||||||||||
Sponsor Name:Medical University of Vienna | ||||||||||||||||||
Full Title: Target tissue concentration of standard antibiotic treatment in coronary artery bypass grafting using left internal mammary artery | ||||||||||||||||||
Medical condition: antibiotic target tissue protection during cardiac surgery with the use of an internal mammary artery graft to prevent deep sternal wound infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-000124-14 | Sponsor Protocol Number: NL47077 | Start Date*: 2014-10-21 |
Sponsor Name:Academic Medical Center | ||
Full Title: Antibiotic prophylaxis to prevent wound infections following implant removal after foot, ankle and lower leg fractures. | ||
Medical condition: Postoperative wound infection following implant removal below the knee | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005526-22 | Sponsor Protocol Number: V4 | Start Date*: 2012-05-14 | ||||||||||||||||||||||||||
Sponsor Name:Medizinische Universität Wien | ||||||||||||||||||||||||||||
Full Title: Tissue concentration of cefazolin and linezolid in sternal spongiosa in elective coronary artery bypass grafting: an in-vivo microdialysis study | ||||||||||||||||||||||||||||
Medical condition: perioperative antibiotic prophylaxis during coronary artery bypass grafting | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: AT (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011775-78 | Sponsor Protocol Number: 08GINE1 | Start Date*: 2009-01-20 |
Sponsor Name:UNIVERSITA` CAMPUS BIOMEDICO | ||
Full Title: Evaluation of efficacy of antibiotic prophylaxis in patients undergoing operative hysteroscopy | ||
Medical condition: Patients needing operative hysteroscopy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001250-28 | Sponsor Protocol Number: RBHP 2011 BONNIN | Start Date*: 2011-06-10 |
Sponsor Name:CHU de Clermont-Ferrand | ||
Full Title: | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002459-40 | Sponsor Protocol Number: BREAST-AB-01 | Start Date*: 2020-12-17 |
Sponsor Name:Rigshospitalet | ||
Full Title: Prophylactic treatment of breast implants with a solution of gentamicin, vancomycin and cefazolin antibiotics for women undergoing breast reconstructive surgery: a randomized controlled trial (The ... | ||
Medical condition: Implant-based breast reconstruction following mastectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004130-25 | Sponsor Protocol Number: DUR001-304 | Start Date*: 2016-03-07 |
Sponsor Name:Durata Therapeutic International B.V. | ||
Full Title: A phase 3, Multicenter, Double-Blind, Randomized, Comparator Controlled Trial of the Safety and Efficacy of Dalbavancin versus Active Comparator in Pediatric Subjects with Acute Hematogenous Osteom... | ||
Medical condition: Acute Hematogenous Osteomyelitis of the Long Bones Known or Suspected to be due to Gram-Positive Organisms | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-001956-40 | Sponsor Protocol Number: PK_pregnancy | Start Date*: 2023-03-05 |
Sponsor Name:Medical University Vienna | ||
Full Title: Antibiotic pharmacokinetics in women with twin pregnancy | ||
Medical condition: The target population are twin pregnancy women that will deliver through c-section and that are receiving one or more of the included antibiotics. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000459-10 | Sponsor Protocol Number: PADIT | Start Date*: 2014-06-10 | |||||||||||
Sponsor Name:Population Health Research Institute (PHRI) | |||||||||||||
Full Title: A cluster Crossover Trial Comparing Conventionl vs Incremental Antibiotic Therapy for the Prevention or Arrhytmia Device Infection | |||||||||||||
Medical condition: high-risk patients undergoing arrhythmia device procedures | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004372-27 | Sponsor Protocol Number: 0112 | Start Date*: 2016-05-17 | |||||||||||
Sponsor Name:Theravance Biopharma Ireland Limited | |||||||||||||
Full Title: A Phase 3 Multicenter, Randomized, Open-label, Clinical Trial of Telavancin Versus Standard Intravenous Therapy in the Treatment of Subjects with Staphylococcus aureus Bacteremia Including Infectiv... | |||||||||||||
Medical condition: Staphylococcus aureus Bacteremia Including Infective Endocarditis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) PL (Completed) LV (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004023-40 | Sponsor Protocol Number: TR701-122 | Start Date*: 2015-05-06 | |||||||||||
Sponsor Name:Cubist Pharmaceuticals, Inc. | |||||||||||||
Full Title: PHASE 3 STUDY OF IV TO ORAL 6-DAY TEDIZOLID PHOSPHATE COMPARED WITH 10-DAY COMPARATOR IN SUBJECTS 12 TO <18 YEARS WITH cSSTI | |||||||||||||
Medical condition: complicated skin and soft tissue infection (cSSTI) | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SI (Completed) BG (Completed) DE (Prematurely Ended) CZ (Completed) LT (Completed) LV (Completed) ES (Completed) PL (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000577-77 | Sponsor Protocol Number: Uni-Koeln-1400 | Start Date*: 2013-07-11 | ||||||||||||||||
Sponsor Name:University of Düsseldorf | ||||||||||||||||||
Full Title: EARLY ORAL SWITCH THERAPY IN LOW-RISK STAPHYLOCOCCUS AUREUS BLOODSTREAM INFECTION ACRONYM: SABATO (Staphylococcus aureus Bacteremia Antibiotic Treatment Options) | ||||||||||||||||||
Medical condition: Low risk Staphylococcus aureus bloodstream infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) ES (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
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