- Trials with a EudraCT protocol (31)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
31 result(s) found for: Beta lactam.
Displaying page 1 of 2.
| 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: 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: 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: 2016-000398-19 | 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: 2019-002327-15 | Sponsor Protocol Number: APHP180596 | Start Date*: 2023-03-15 |
| Sponsor Name:APHP | ||
| Full Title: Beta-lactam Intermittent versus Continuous infusion and Combination antibiotic therapy in Sepsis | ||
| Medical condition: Beta-lactam Intermittent vs Continuous infusion and Combination antibiotic therapy in Sepsis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-006908-32 | Sponsor Protocol Number: PNEUMONOVA | Start Date*: 2022-07-01 | |||||||||||
| Sponsor Name:Sonia Luque Pardos | |||||||||||||
| Full Title: Intrapulmonary penetration of ceftolozane / tazobactam and ceftazidime / avibactam administered in continuous infusion in critically ill patients with nosocomial pneumonia | |||||||||||||
| Medical condition: Nosocomial pneumonia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 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: 2019-001997-27 | Sponsor Protocol Number: ATB_DF_001 | Start Date*: 2020-07-17 | |||||||||||
| Sponsor Name:Institut klinické a experimentální medicíny | |||||||||||||
| Full Title: Rationalisation of ATB therapy in diabetic foot infection and its impact on the intestinal microbiota | |||||||||||||
| Medical condition: Diabetic foot infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 2021-003511-25 | Sponsor Protocol Number: LOCAL/2020/CR-03 | Start Date*: 2021-11-25 | |||||||||||
| Sponsor Name:Nimes University Hospital | |||||||||||||
| Full Title: PNEUMONIA DOSING IN CRITICALLY ILL PATIENTS A multicentre study to define novel individualised dosing regimens to maximise antibiotic effectiveness for treatment of pneumonia in ICU « French cohort... | |||||||||||||
| 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: 2017-002110-32 | Sponsor Protocol Number: 10-0065 | Start Date*: 2018-06-13 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Regents of the University of Michigan | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: DMID Protocol Number: 10-0065 OVERCOME Trial: Randomized Controlled Trial for the Treatment of Extensively Drug-Resistant Gram-negative Bacilli | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Blood stream Infection (BSI) and/or pneumonia due to extensively drug-resistant Gram-negative bacilli (XDR-GNB) including XDR-AB, CRE and XDR-PA | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: BG (Completed) GR (Completed) IT (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 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: 2005-004211-30 | Sponsor Protocol Number: 2005-23 | Start Date*: 2005-10-17 |
| Sponsor Name:The Norwegian Radium Hospital | ||
| Full Title: Penicillin G and an aminoglycoside versus meropenem as initial empiric antibiotic therapy in lymphoma and leukemia patients with febrile neutropenia | ||
| Medical condition: Lymphoma and leukemia patients with febrile neutropenia | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (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: 2012-000726-21 | Sponsor Protocol Number: D4280C00006 | Start Date*: 2012-09-11 | ||||||||||||||||
| Sponsor Name:AstraZeneca AB | ||||||||||||||||||
| Full Title: An Open-Label, Randomized, Multicenter, Phase III Study of Ceftazidime Avibactam (CAZ-AVI, formerly CAZ104) and Best Available Therapy for the Treatment of Infections Due to Ceftazidime Resistant G... | ||||||||||||||||||
| Medical condition: cUTI, Complicated Urinary Tract Infection, cIAI, Complicated intra-abdominal infection | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) DE (Completed) CZ (Completed) ES (Completed) GR (Completed) BG (Completed) HU (Completed) IT (Completed) GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-004328-43 | Sponsor Protocol Number: MK-7655A-020 | Start Date*: 2017-09-19 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
| Full Title: A Phase 1b, Open-label, Single-dose Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of MK-7655A in Pediatric Subjects From Birth to Less Than 18 Years of Age With Confirmed or Susp... | |||||||||||||
| Medical condition: Treatment of bacterial infections in pediatric populations | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) PL (Completed) Outside EU/EEA GB (Completed) BG (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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