- Trials with a EudraCT protocol (74)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (17)
74 result(s) found for: Escherichia.
Displaying page 1 of 4.
EudraCT Number: 2015-005706-11 | Sponsor Protocol Number: Cyst2016_01 | Start Date*: 2016-03-14 | |||||||||||
Sponsor Name:Vita Green Europa S.A. | |||||||||||||
Full Title: Single-site, open, randomized clinical trial to assess the non-inferiority of Cysticlean® versus Fosfomicina in the treatment of cystitis in women in Spain. | |||||||||||||
Medical condition: Urinary Tract Infection (UTI) | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001448-78 | Sponsor Protocol Number: Cyst2018_01 | Start Date*: 2018-11-08 | |||||||||||
Sponsor Name:Vita Green Europa S.A. | |||||||||||||
Full Title: Single-site, open, randomized clinical trial to assess the non-inferiority of Cysticlean® versus Fosfomicina in the treatment of cystitis in women in Spain. | |||||||||||||
Medical condition: Urinary Tract Infection (UTI) | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021413-23 | Sponsor Protocol Number: 07-0036 | Start Date*: 2010-09-28 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University of Athens, Medical School | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Optimizing Dosing of Colistin for Infections Resistant to all Other Antibiotics | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Bloodstream infection (bacteremia) or hospital-acquired pneumonia by Gram-negative bacillus lacking susceptibility to all of the following antibiotics: cefepime OR ceftazidime, imipenem OR meropene... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GR (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005273-27 | Sponsor Protocol Number: VAC52416BAC3001 | Start Date*: 2021-09-07 | ||||||||||||||||
Sponsor Name:Janssen Vaccines & Prevention B.V | ||||||||||||||||||
Full Title: Randomized, Double-Blind, Placebo-controlled, Multicenter Phase 3 Study to Assess the Efficacy, Safety And Immunogenicity of Vaccination With ExPEC9V in the Prevention of Invasive Extraintestinal P... | ||||||||||||||||||
Medical condition: Invasive Extraintestinal Pathogenic Escherichia coli Disease | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Trial now transitioned) ES (Ongoing) NL (Trial now transitioned) IT (Prematurely Ended) CZ (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002690-35 | Sponsor Protocol Number: OEV123 | Start Date*: 2017-05-08 | ||||||||||||||||
Sponsor Name:Scandinavian Biopharma AB | ||||||||||||||||||
Full Title: A randomized, placebo-controlled phase IIb (OEV 123) study to evaluate safety, immunogenicity, diagnostic methodology, and estimate vaccine efficacy of an oral enterotoxigenic Escherichia coli (ET... | ||||||||||||||||||
Medical condition: Healthy voluteers (prevention of diarrheal disease due to infection with enterotoxigenic E. coli [ETEC]) | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: View results |
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 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BG (Completed) GR (Completed) IT (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002922-21 | Sponsor Protocol Number: FOREST | Start Date*: 2014-05-07 | |||||||||||
Sponsor Name:FISEVI | |||||||||||||
Full Title: Randomized, phase III, multicentre, open-labelled clinical trial, to evaluate the efficacy of fosfomycin vs meropenem in the treatment of bacteremic urinary tract infection caused by Escherichia co... | |||||||||||||
Medical condition: Bacteremic urinary tract infection by Escherichia coli extended spectrum beta-lactamase (ESBL). | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002222-46 | Sponsor Protocol Number: 36688 | Start Date*: 2013-09-04 | |||||||||||||||||||||||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | |||||||||||||||||||||||||||||||||
Full Title: In vivo effects of C1-esterase inhibitor on innate immune response during endotoxemia in human - VECTOR-II study A randomized controlled pilot study | |||||||||||||||||||||||||||||||||
Medical condition: Inflammation, SIRS and endotoxemia | |||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-001240-19 | Sponsor Protocol Number: CSL16001 | Start Date*: 2016-08-22 |
Sponsor Name:Synlogic | ||
Full Title: Clearance of the probiotic strain Escherichia coli Nissle 1917 in the gastrointestinal tract of healthy volunteers | ||
Medical condition: Healthy volunteers trial, intended indication: Colitis ulcerosa in phase of remission, Chronic constipation | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BG (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-001541-13 | Sponsor Protocol Number: OEV-125 | Start Date*: 2021-07-27 | ||||||||||||||||
Sponsor Name:Scandinavian Biopharma Holding AB | ||||||||||||||||||
Full Title: A Phase 2 immunological bridging study assessing the non-inferiority of a new formulation of ETVAX®. A prospective double-blind, randomized study in healthy volunteers | ||||||||||||||||||
Medical condition: Healthy volunteers (prevention of diarrheal disease due to infection with enterotoxigenic E. coli [ETEC]) | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-003792-19 | Sponsor Protocol Number: FOS-PROST-001 | Start Date*: 2021-03-04 |
Sponsor Name:Hospital Universitari Mutua Terrassa | ||
Full Title: Fosfomycin as an oral alternative treatment for acute bacterial prostatitis due to multi-drug resistant Escherichia coli. Pilot study | ||
Medical condition: Acute bacterial prostatitis due to multi-drug resistant Escherichia coli | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004531-36 | Sponsor Protocol Number: MU1646 | Start Date*: 2018-09-03 |
Sponsor Name:Ardeypharm GmbH | ||
Full Title: Escherichia coli strain Nissle 1917 - Suspension for treatment of patients with Clostridium difficile associated diarrhoea | ||
Medical condition: Clostridium difficile associated diarrhoea (CDAD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002691-17 | Sponsor Protocol Number: C11-001 | Start Date*: 2011-07-06 | |||||||||||
Sponsor Name:ALEXION PHARMA INTERNATIONAL SARL | |||||||||||||
Full Title: An open label, multi-center trial of eculizumab in patients with Shiga-toxin producing Escherichia Coli Hemolytic-Uremic Syndrome (STEC-HUS) | |||||||||||||
Medical condition: Shiga-Toxin producing Escherichia Coli Hemolytic-Uremic Syndrome | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002343-99 | Sponsor Protocol Number: 1.0 | Start Date*: 2012-01-03 |
Sponsor Name:Heart of England NHS Foundation Trust | ||
Full Title: An Open-label Study into the Efficacy and Dosing of Probiotic Escherichia coli Nissle 1917 for Prevention of Gram-negative Gastric Colonisation in Ventilated Intensive Care Patients. | ||
Medical condition: Gastric colonisation by pathogenic gram negative bacteria in ventilated adult ICU patients and it's prevention by the probiotic E.coli Nissle 1917 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011446-26 | Sponsor Protocol Number: 2009-011446-26 | Start Date*: 2011-07-04 |
Sponsor Name:Uppsala University | ||
Full Title: A randomized, placebo-controlled, double blind, parallel group phase II study of anti-ESBL IgY for the eradication of ESBL Klebsiella pneumoniae and Escherichia coli in faeces in carriers | ||
Medical condition: Feacal carriage of ESBL producing Klebsiella pneumoniae and/or E. coli. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004626-28 | Sponsor Protocol Number: SymSF2 | Start Date*: 2019-07-18 |
Sponsor Name:SymbioPharm GmbH | ||
Full Title: Randomized, double-blind, placebo-controlled, multi-centre trial to evaluate the efficacy, safety and tolerability of oral treatment with living bacteria of E. coli DSM 17252 (Symbioflor®2) in pati... | ||
Medical condition: Diarrhoea-predominant irritable bowel syndrome with recurrent abdominal pain according to Rome IV criteria | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003793-26 | Sponsor Protocol Number: 3066K1-3311-WW | Start Date*: 2008-05-19 | |||||||||||
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc. | |||||||||||||
Full Title: Phase 3b, Randomized, Open-Label Study of Bevacizumab + Temsirolimus vs. Bevacizumab + Interferon-Alfa as First-Line Treatment in Subjects With Advanced Renal Cell Carcinoma | |||||||||||||
Medical condition: First-Line Treatment in Subjects with Advanced Renal Cell Carcinoma | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) ES (Completed) FR (Completed) BE (Completed) PT (Completed) CZ (Completed) DE (Completed) SK (Completed) NL (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000868-34 | Sponsor Protocol Number: ZKES-EcNO-2015 | Start Date*: 2015-05-29 |
Sponsor Name:ZKES GmbH | ||
Full Title: Randomized, placebo controlled phase III trial of a microbiological concomitant therapy/prevention of chemotherapeutical induced diarrhea (caused by inflammation and an impaired intestinal barrier)... | ||
Medical condition: Gastric or colorectal cancers, where a treatment with 5-Fluoruracil and one further chemotherapeutic remedy (either irinotecan or a platinum based chemotherapeutic remedy) is planned. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004961-14 | Sponsor Protocol Number: UV2013/4 | Start Date*: 2014-06-11 | |||||||||||
Sponsor Name:Kliniken Kärnan Urology Centre | |||||||||||||
Full Title: Pilot study to investigate the mode of action (MoA) of Uro-Vaxom® on a molecular level in pre-menopausal women suffering from recurrent urinary tract infections (rUTI) | |||||||||||||
Medical condition: Recurrent urinary tract infections (rUTI) | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006335-12 | Sponsor Protocol Number: Ecorhino | Start Date*: 2008-11-18 |
Sponsor Name:Prof. Dr. med. Margitta Worm | ||
Full Title: Explorative analysis of the immunmodulatory capacities of apathogenic Escherichia coli Nissle 1917 in patients with rhinoconjunctivitis due to grass pollen allergy. | ||
Medical condition: Due to the worldwide increasing prevalence of allergic rhinoconjunctivitis (AR), new therapeutical strategies are needed. The symptomatic treatment with topical and systemic antihistamines and cort... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
