- Trials with a EudraCT protocol (13)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (10)
13 result(s) found for: vre.
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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 (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002346-32 | Sponsor Protocol Number: SB-2-004-005 | Start Date*: 2015-11-27 | |||||||||||
Sponsor Name:Synthetic Biologics, Inc. | |||||||||||||
Full Title: A Phase 2b Parallel-Group, Double-Blind, Placebo-Controlled, Multicenter Study of SYN-004 Compared to Placebo for the Prevention of Clostridium difficile Associated Diarrhea in Patients with a Diag... | |||||||||||||
Medical condition: Prevention of Clostridium difficile infection (CDI), Clostridium difficile associated diarrhea (CDAD), antibiotic-associated diarrhea (AAD) and secondary infections with healthcare-acquired drug-re... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) PL (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001900-76 | Sponsor Protocol Number: PRASCO | Start Date*: 2015-08-25 | |||||||||||
Sponsor Name:UMBERTO I - POLICLINICO DI ROMA | |||||||||||||
Full Title: Manipulating the microbiome in IBD by antibiotics and fecal microbiota transplantation (FMT): a randomized controlled trial | |||||||||||||
Medical condition: Acute Severe colitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005483-25 | Sponsor Protocol Number: SMT19969/C003 | Start Date*: 2014-10-08 | |||||||||||
Sponsor Name:Summit (Oxford) Limited | |||||||||||||
Full Title: A Phase II, Randomized, Open-Label, Active-Controlled Clinical Study to Investigate the Safety and Efficacy of SMT19969 (200 mg BID) for 10 days Compared with Fidaxomicin (200 mg BID) for 10 days f... | |||||||||||||
Medical condition: Clostridium difficile infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004333-42 | Sponsor Protocol Number: SISPCT | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Friedrich-Schiller-University of Jena | |||||||||||||
Full Title: Prospective randomized clinical multicenter trial about the effect of an adjunctive intravenous treatment with sodium selenite (selenase®T, double-blind) and a procalcitonin guided causal therapy (... | |||||||||||||
Medical condition: severe sepsis / septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002604-41 | Sponsor Protocol Number: WP6-282512 | Start Date*: 2014-01-31 |
Sponsor Name:University Medical Centre Utrech | ||
Full Title: RGNOSIS: Ecological Effects of Decolonisation Strategies in Intensive Care | ||
Medical condition: Colonisation and Infection with (multi drug resistant) Gram negative bacteria in ICU patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000875-37 | Sponsor Protocol Number: VanC-IT | Start Date*: 2022-11-03 | |||||||||||
Sponsor Name:UNIVERSITÀ DEGLI STUDI MILANO BICOCCA | |||||||||||||
Full Title: A Prospective, Randomized, Placebo-controlled Clinical Trial of oral vancomycin in adults and young adults (15-17 years old) affected by Primary Sclerosing Cholangitis with or without Inflammatory ... | |||||||||||||
Medical condition: Primary Sclerosing Cholangitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000508-13 | Sponsor Protocol Number: 72779 | Start Date*: 2020-10-27 | |||||||||||
Sponsor Name:Princess Máxima Center for Pediatric Oncology | |||||||||||||
Full Title: An open-label, randomized clinical trial on teicoplanin infection prophylaxis in pediatric patients with acute myeloid leukemia | |||||||||||||
Medical condition: Acute myeloid leukemia | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) BE (Ongoing) DK (Ongoing) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000203-89 | Sponsor Protocol Number: NeoVanc | Start Date*: 2016-07-18 | |||||||||||
Sponsor Name:Fondazione PENTA Onlus | |||||||||||||
Full Title: Multi-centre, randomised, open label, phase IIb study to compare the efficacy, safety and pharmacokinetics (PK) of an optimised dosing to a standard dosing regimen of vancomycin in neonates and inf... | |||||||||||||
Medical condition: Neonatal late onset sepsis | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) IT (Prematurely Ended) EE (Ongoing) ES (Prematurely Ended) GR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005281-30 | Sponsor Protocol Number: DUR001-306 | Start Date*: 2016-11-03 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Allergan Ltd. | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 3, Multicenter, Open-Label, Randomized, Comparator Controlled Trial of the Safety and Efficacy of Dalbavancin versus Active Comparator in Pediatric Subjects with Acute Bacterial Skin and Sk... | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Acute bacterial skin and skin structure infection. For Cohort 5 (from birth to less than 3 months) also patients with sepsis are allowed. | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: LV (Prematurely Ended) LT (Prematurely Ended) ES (Prematurely Ended) BG (Completed) GR (Ongoing) PL (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003048-21 | Sponsor Protocol Number: Uni-Köln-1667 | Start Date*: 2014-03-10 | |||||||||||||||||||||||||||||||
Sponsor Name:University of Cologne | |||||||||||||||||||||||||||||||||
Full Title: CONTROLING INTESTINAL COLONIZATION OF HIGH-RISK PATIENTS WITH EXTENDED- SPECTRUM BETALACTAMASE PRODUCING ENTEROBACTERIACEAE (ESBL-E) – A RANDOMIZED TRIAL (CLEAR) | |||||||||||||||||||||||||||||||||
Medical condition: Immunocompromised patients at high risk of bloodstream infections with colonizing bacteria. | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-001200-12 | Sponsor Protocol Number: A5951002 | Start Date*: 2007-08-27 | |||||||||||
Sponsor Name:Pfizer Global Research and Development | |||||||||||||
Full Title: Linezolid In The Treatment Of Complicated Skin And Soft Tissue Infections Proven To Be Due To Methicillin-Resistant Staphylococcus Aureus | |||||||||||||
Medical condition: Complicated skin and soft tissue infections | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (Completed) ES (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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 |
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