- Trials with a EudraCT protocol (16)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
16 result(s) found for: Beta lactam antibiotics.
Displaying page 1 of 1.
EudraCT Number: 2011-006107-35 | Sponsor Protocol Number: AGO/2011/012 | Start Date*: 2012-03-09 | |||||||||||
Sponsor Name:Ghent University Hospital | |||||||||||||
Full Title: Pharmacokinetics of small spectcrum beta-lactam antibiotics (Amoxicillin/Clavulanic Acid and Cefuroxime) on intensive care. | |||||||||||||
Medical condition: Patients who are hospitalised on the Intensive Care Unit, and who are treated with Amoxicillin/Clavulanic acid or Cefuroxime, because of an infection. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000398-19 | Sponsor Protocol Number: AGO/2016/002 | Start Date*: 2016-03-08 |
Sponsor Name:Ghent University | ||
Full Title: Pilot study: pharmacokinetics of beta-lactam antibiotics, piperacillin-tazobactam, ceftazidim and meropenem in blood and sputum of cystic fibrosis patients. | ||
Medical condition: Cystic fibrosis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004637-85 | Sponsor Protocol Number: TGI-CCT254643 | Start Date*: 2019-02-06 | |||||||||||
Sponsor Name:The George Institute for Global Health | |||||||||||||
Full Title: A phase III randomised controlled trial of continuous beta-lactam infusion compared with intermittent beta-lactam dosing in critically ill patients | |||||||||||||
Medical condition: Sepsis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004677-14 | Sponsor Protocol Number: DIABOLO | Start Date*: 2018-03-09 |
Sponsor Name:Erasmus MC | ||
Full Title: Dose IndividualizAtion of Beta-lactam and fluOroquinoLone AntiBiotics in ICU patients: to TDM or not to TDM and the effects on Outcome (DIABOLO-study) | ||
Medical condition: ICU patients with infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000809-36 | Sponsor Protocol Number: CAP-IT | Start Date*: 2016-09-30 |
Sponsor Name:Medical Research Council Clinical Trials Unit at UCL | ||
Full Title: Efficacy, safety and impact on antimicrobial resistance of duration and dose of amoxicillin treatment for young children with Community-Acquired Pneumonia (CAP): a randomised controlled trial. | ||
Medical condition: Pneumonia | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) IE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001609-89 | Sponsor Protocol Number: DORI-10 | Start Date*: 2005-04-26 |
Sponsor Name:Peninsula Pharmaceuticals, Inc | ||
Full Title: A Multicenter, Randomized, Open-Label Phase 3 Study to Compare the Safety and Efficacy of Intravenous Doripenem with that of Intravenous Imipenem in Ventilator-Associated Pneumonia | ||
Medical condition: patients diagnosed with ventilator-associated pneumonia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) EE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-002562-23 | Sponsor Protocol Number: 2015-768 | Start Date*: 2017-06-27 | |||||||||||
Sponsor Name:Hvidore Hospital | |||||||||||||
Full Title: Therapeutic drug monitoring and continuous infusion of beta-lactam antibiotics in patients with bacteraemia. | |||||||||||||
Medical condition: Bacteraemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-003582-38 | Sponsor Protocol Number: LOCAL/2022/CR-01 | Start Date*: 2023-04-06 | |||||||||||
Sponsor Name:NIMES UNIVERSITY HOSPITAL | |||||||||||||
Full Title: THE SPARSE PNEUDOS STUDY : A multi-centre study to define novel individualised dosing regimens to maximise antibiotic effectiveness for treatment of pneumonia in ICU | |||||||||||||
Medical condition: Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003727-22 | Sponsor Protocol Number: CER13266 | Start Date*: 2015-05-26 | |||||||||||||||||||||
Sponsor Name:Geneva University Hospitals | |||||||||||||||||||||||
Full Title: A randomized controlled multicenter trial of a five day course of oral colistin and neomycin followed by restoration of the gut microbiota using fecal transplantation to eradicate intestinal carr... | |||||||||||||||||||||||
Medical condition: Intestinal colonization with extended-spectrum beta-lactamse or carbapenemase producing enterobacteriaceae | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002478-37 | Sponsor Protocol Number: 61682 | Start Date*: 2018-01-11 |
Sponsor Name:VU University Medical Center | ||
Full Title: Right Dose, Right Now: Randomized Clinical Trial | ||
Medical condition: Infectious disease, sepsis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000970-10 | Sponsor Protocol Number: LPS16140 | Start Date*: 2020-09-09 | |||||||||||
Sponsor Name:Sanofi Aventis Groupe | |||||||||||||
Full Title: Phase III, randomized, double blind, parallel groups, clinical trial to evaluate the efficacy and safety of Bacillus clausii versus placebo in the prevention of antibiotic associated diarrhea (AAD)... | |||||||||||||
Medical condition: Antibiotic associated diarrhea (AAD) in children | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002587-28 | Sponsor Protocol Number: 2019-5165 | Start Date*: 2020-02-25 |
Sponsor Name:Radboudumc | ||
Full Title: ABSORB 2:An exploratie study determining the oral antibiotic drug absorption in patients with short bowel syndrome. | ||
Medical condition: short bowel syndrome, home parenteral nutrition | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001033-12 | Sponsor Protocol Number: 12020 | Start Date*: 2020-10-13 | |||||||||||
Sponsor Name:Niels Eske Bruun | |||||||||||||
Full Title: PROPHYLACTIC ANTIBIOTIC TREATMENT IN END-STAGE KIDNEY DISEASE AND CENTRAL VENOUS CATHETER AS HEMODIALYSIS VASCULAR ACCESS | |||||||||||||
Medical condition: Severe infection in patients end stage kidney disease and in hemodialysis with CVC as vascular asscess. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003529-13 | Sponsor Protocol Number: 010617 | Start Date*: 2017-10-19 | |||||||||||
Sponsor Name:Thomas Benfield | |||||||||||||
Full Title: Efficacy of seven and fourteen days of antibiotic treatment in uncomplicated Staphylococcus aureus bacterermia: A randomized, non-blinded, non-inferiority interventional study | |||||||||||||
Medical condition: Staphylococcus aureus bacteremia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000404-15 | Sponsor Protocol Number: 34666 | Start Date*: 2019-04-29 | |||||||||||
Sponsor Name:Thomas Benfield | |||||||||||||
Full Title: Shortened Antibiotic Treatment in Community-Acquired Pneumonia: A Nationwide Danish Randomized Controlled Trial | |||||||||||||
Medical condition: Community-acquired pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001515-31 | Sponsor Protocol Number: NEOMERO-1 | Start Date*: 2011-08-25 | |||||||||||
Sponsor Name:FONDAZIONE PENTA ONLUS | |||||||||||||
Full Title: EFFICACY, PHARMACOKINETICS AND SAFETY OF MEROPENEM IN INFANTS BELOW 90 DAYS OF AGE (INCLUSIVE) WITH CLINICAL OR CONFIRMED LATE-ONSET SEPSIS: A EUROPEAN MULTICENTER RANDOMISED PHASE III TRIAL | |||||||||||||
Medical condition: late onset sepsis in the neonate and infant up to 90 days of age | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) GR (Completed) LT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
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