- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: Clostridioides.
Displaying page 1 of 1.
| EudraCT Number: 2021-005473-10 | Sponsor Protocol Number: BEYOND | Start Date*: 2021-11-24 | |||||||||||
| Sponsor Name:Hellenic Institute for the Study of Sepsis | |||||||||||||
| Full Title: BEZLOTOXUMAB YIELDED OUTCOMES BY ADDRESSING PERSONALIZED NEEDS IN CLOSTRIDIOIDES DIFFICILE INFECTION: THE BEYOND DOUBLE-BLIND RANDOMIZED CLINICAL TRIAL | |||||||||||||
| Medical condition: Clostridioides difficile Infection (CDI) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004591-17 | Sponsor Protocol Number: ICD-01 | Start Date*: 2021-04-23 | |||||||||||
| Sponsor Name:Mikrobiomik Healthcare Company S.L. | |||||||||||||
| Full Title: A randomised, controlled, open-label phase III clinical trial in patients with recurrent Clostridioides difficile (CD) infection, to evaluate the efficacy and safety of capsules of lyophilised faec... | |||||||||||||
| Medical condition: Recurrent Clostridioides difficile (CD) infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002677-57 | Sponsor Protocol Number: PREVAN | Start Date*: 2021-11-04 | |||||||||||
| Sponsor Name:Dra. Julia Origüen Sabater | |||||||||||||
| Full Title: A phase III, multicenter, randomized, double-blind clinical trial to evaluate the efficacy and safety of oral vancomycin versus placebo in preventing relapse of Clostridioides difficile infection i... | |||||||||||||
| Medical condition: Patients at high risk of recurrence due to CDI who require hospitalization and who increase morbidity and mortality from new CDI. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-002845-39 | Sponsor Protocol Number: Infmed1 | Start Date*: 2019-10-02 | |||||||||||
| Sponsor Name:Aalborg University Hospital | |||||||||||||
| Full Title: Partial oral antibiotic treatment for bacterial brain abscess: An open-label randomised non-inferiority trial (ORAL) | |||||||||||||
| Medical condition: Brain abscess | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Trial now transitioned) FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-004924-14 | Sponsor Protocol Number: BSTEP | Start Date*: 2022-04-21 | |||||||||||||||||||||
| Sponsor Name:Leiden University Medical Center | |||||||||||||||||||||||
| Full Title: New treatment strategy for patients with multiple recurrent Clostridioides difficile infection with bezlotoxumab as first option | |||||||||||||||||||||||
| Medical condition: recurrent C. difficile infection | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2021-003847-10 | Sponsor Protocol Number: SHORTENII | Start Date*: 2022-01-12 | ||||||||||||||||
| Sponsor Name:Fundación Pública Andaluza para la Gestión de la Investigación en Salud de Sevilla (FISEVI) | ||||||||||||||||||
| Full Title: Efficacy and safety of 7 versus 14 days of antibiotic treatment for Pseudomonas aeruginosa bacteraemia: a multicentre, randomized clinical trial (SHORTEN-2) with a DOOR/RADAR analysis | ||||||||||||||||||
| Medical condition: Adult patients with bloodstream infections produced by Pseudomonas aeruginosa. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
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