- Trials with a EudraCT protocol (58)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
58 result(s) found for: Antibiotic resistant bacteria.
Displaying page 1 of 3.
EudraCT Number: 2019-000244-10 | Sponsor Protocol Number: EGBAB | Start Date*: 2019-12-13 |
Sponsor Name:Region Uppsala | ||
Full Title: Influence of antibiotic treatment on the normal flora and the presence of resistance genes in known carriers of ESBL and VRE | ||
Medical condition: Carriage of genes coding for vancomycin resistant enterococci (VRE) and extended spectrum betalactamase producing enterobacteriales (EPE) phenotypes. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023889-52 | Sponsor Protocol Number: AntiResDev-SWE | Start Date*: 2011-01-18 |
Sponsor Name:Karolinska Universitetssjukhuset | ||
Full Title: Effects of Clindamycin and Ciprofloxacin administration on the emergence, prevalence and persistence of antibiotic-resistant bacteria in humans | ||
Medical condition: To assess the effect of ciprofloxacin and clindamycin administration on the proportions and types of cultivable antibiotic-resistant bacteria that emerge in the oropharynx, on the skin and in the... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003704-31 | Sponsor Protocol Number: ARG-16 | Start Date*: 2019-05-17 |
Sponsor Name:Uppsala University | ||
Full Title: Impact on the intestinal microbiota during antibiotic treatment | ||
Medical condition: Impact on the intestinal microbiota during antibiotic treatment | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002388-33 | Sponsor Protocol Number: ZKSJ0086 | Start Date*: 2016-09-05 |
Sponsor Name:Friedrich-Schiller-University Jena | ||
Full Title: Therapeutic drug monitoring (TDM) for personalized antibiotic treatment with piperacillin-tazobactam (PipTaz) in patients with febrile neutropenia after myelo-suppressive cytostatic chemotherapy | ||
Medical condition: Patients with febrile neutropenia after myelo-suppressive chemotherapy treated with piperacillin/tazobactam | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-000953-30 | Sponsor Protocol Number: EPAAC | Start Date*: 2019-07-25 |
Sponsor Name:Uppsala University Hospital | ||
Full Title: Effects of phenoximetylpenicillin, amoxicillin and amoxicillin-clavulanic acid on the gut microbiota of healthy volunteers: a randomized clinical trail | ||
Medical condition: Effects of phenoximetylpenicillin, amoxicillin and amoxicillin-clavulanic acid on the gut microbiota of healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004800-71 | Sponsor Protocol Number: 1230_OPBG_2016 | Start Date*: 2017-04-07 |
Sponsor Name:Bambino Gesù Children's Hospital | ||
Full Title: Determination of intraoperative levels of Cefoxitin during cardiac surgery requiring cardiopulmonary bypass in neonates, infants, children below, and above 40 kg. | ||
Medical condition: Antibiotic prophylaxis for surgical procedure using cardiopulmonary bypass in children with congenital heart disease. | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004819-31 | Sponsor Protocol Number: 1787/12 | Start Date*: 2013-07-08 | |||||||||||
Sponsor Name:RADBOUD UNIVERSITY NIJMEGEN MEDICAL CENTER | |||||||||||||
Full Title: Multicenter open-label RCT to compare colistin alone vs. colistin plus meropenem | |||||||||||||
Medical condition: INFECTIONS DUE TO CARBAPENEM RESISTENT GRAM NEGATIVE BACTERIA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001054-17 | Sponsor Protocol Number: PHRN15-SE/AMIKINHAL | Start Date*: 2017-01-27 | |||||||||||
Sponsor Name:CHRU de Tours | |||||||||||||
Full Title: Double-blinded multicenter randomized controlled trial comparing inhaled amikacin versus placebo to prevent ventilator associated pneumonia | |||||||||||||
Medical condition: Patient with mechanical ventilation through an endotracheal tube | |||||||||||||
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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: 2017-000445-51 | Sponsor Protocol Number: CHB17.01 | Start Date*: 2018-03-23 |
Sponsor Name:Centre Henri Becquerel | ||
Full Title: Efficiency of an antibioprophylaxy (levofloxacin) in patient treated by azacitidine | ||
Medical condition: myelodysplastic syndrome or acute myeloid leukeamia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017647-34 | Sponsor Protocol Number: ANTIRESDEV | Start Date*: 2010-03-29 | |||||||||||
Sponsor Name:Helperby Therapeutics | |||||||||||||
Full Title: Effect of minocycline and amoxicillin administration on the prevalence of antibiotic resistant bacteria and on the indigenous oral, faecal, cutaneous and nasal microbiotas. | |||||||||||||
Medical condition: Amoxicillin and Minocycline are marketed antibiotic to fight bacterial infections. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004402-10 | Sponsor Protocol Number: APHP180587 | Start Date*: 2020-03-11 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Fecal transplantation to Eradicate Colonizing Emergent Superbugs | |||||||||||||
Medical condition: Patients colonized with MDR-GNB (multi-drug resistant Gram Negative bacteria ) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000405-23 | Sponsor Protocol Number: 2013-000405-23 | Start Date*: 2013-06-12 | |||||||||||
Sponsor Name:Karolinska University Hospital | |||||||||||||
Full Title: Susceptibility changes among oral microorganisms following single dose antibiotic prophylaxis | |||||||||||||
Medical condition: Changes in antibiotic susceptibility among oral commensal microflora following a single dose administration of amoxicillin | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002148-95 | Sponsor Protocol Number: SHORTEN | Start Date*: 2014-05-21 | |||||||||||
Sponsor Name:Fundación Pública Andaluza para la Gestión en Salud de Sevilla (FISEVI) | |||||||||||||
Full Title: Optimal duration of the antimicribial treatment for bloodstream infections produced by Enterobacteriaceae. Clinical trial "SHORTEN". | |||||||||||||
Medical condition: Adult patients with bloodstream infections produced by Enterobacteriaceae. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004154-22 | Sponsor Protocol Number: TR701-132 | Start Date*: 2014-04-17 | |||||||||||
Sponsor Name:Trius Therapeutics, a Wholly Owned Subsidiary of Cubist Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3 Randomized Double-blind Study Comparing TR 701 FA and Linezolid in Ventilated Gram-positive Nosocomial Pneumonia | |||||||||||||
Medical condition: Ventilated Gram-positive nosocomial pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) HU (Completed) AT (Completed) DE (Completed) BE (Completed) ES (Completed) GR (Completed) SK (Completed) CZ (Completed) EE (Completed) GB (Completed) HR (Completed) PT (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001324-33 | Sponsor Protocol Number: APHP200392 | Start Date*: 2020-04-09 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS (APHP) | |||||||||||||
Full Title: Use of a respiratory multiplex PCR and procalcitonin to reduce antibiotic exposure in patients with severe confirmed COVID-19 pneumonia : a multicenter, parallel-group, open-label, randomized contr... | |||||||||||||
Medical condition: Severe confirmed COVID-19 pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000735-41 | Sponsor Protocol Number: 2015_66 | Start Date*: 2016-09-06 | |||||||||||
Sponsor Name:CHRU LILLE | |||||||||||||
Full Title: Antimicrobial treatment in patients with ventilator-associated tracheobronchitis: a prospective randomized placebo-controlled double-blind multicenter trial | |||||||||||||
Medical condition: ventilator-associated pneumonitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004544-38 | Sponsor Protocol Number: C3601009 | Start Date*: 2020-07-03 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: A PROSPECTIVE, RANDOMIZED, OPEN-LABEL, COMPARATIVE STUDY TO ASSESS THE EFFICACY, SAFETY AND TOLERABILITY OF AZTREONAM-AVIBACTAM (ATM-AVI) AND BEST AVAILABLE THERAPY FOR THE TREATMENT OF SERIOUS INF... | |||||||||||||
Medical condition: SERIOUS INFECTIONS DUE TO MULTI-DRUG RESISTANT GRAM- NEGATIVE BACTERIA PRODUCING METALLO-Β-LACTAMASE (MBL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Prematurely Ended) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003282-17 | Sponsor Protocol Number: 190801 | Start Date*: 2020-02-11 | |||||||||||
Sponsor Name:Thomas Benfield | |||||||||||||
Full Title: Short course antibiotic treatment of Gram-negative bacteremia: A multicenter, randomized, non-blinded, non-inferiority interventional study | |||||||||||||
Medical condition: Gram-negative 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: 2020-003159-13 | Sponsor Protocol Number: ACACIA | Start Date*: 2020-09-15 | |||||||||||
Sponsor Name:CHU DE POITIERS | |||||||||||||
Full Title: Amoxicillin-clavulanate alone or in combination with Ciprofloxacin in Low-Risk Febrile Neutropenic adult Patients: A Prospective, Double-blind, Randomized, Non-Inferiority Multicenter, Phase III C... | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
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