- Trials with a EudraCT protocol (20)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
20 result(s) found for: Broad spectrum antibiotics.
Displaying page 1 of 1.
EudraCT Number: 2007-007640-10 | Sponsor Protocol Number: J&P002/2007 | Start Date*: 2009-01-28 |
Sponsor Name:PD Dr. med. K-H. Konz | ||
Full Title: Tissue pharmacokinetics of daptomycin measured by in vivo microdialysis in patients with diabetic foot infection | ||
Medical condition: A group of adult male or female patients with documented diabetes and bacterial soft tissue infection of the foot who must be subjected to undergo intravenous antimicrobial therapy with broad-spect... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-006949-75 | Sponsor Protocol Number: J&P005/2008 | Start Date*: 2009-08-13 |
Sponsor Name:Medical University Graz, Department for Plastic Surgery | ||
Full Title: Tissue pharmacokinetics of daptomycin measured by in vivo microdialysis in patients with diabetic foot infection | ||
Medical condition: A group of adult male or female patients with documented diabetes and bacterial soft tissue infection of the foot who must be subjected to undergo intravenous antimicrobial therapy with broad spect... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
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: 2007-002876-32 | Sponsor Protocol Number: AAD-CDD-001 | Start Date*: 2008-10-06 | |||||||||||
Sponsor Name:University of Wales Swansea | |||||||||||||
Full Title: A multicentre, randomised, placebo controlled trial of lactic acid bacteria in the prevention of antibiotic-associated diarrhoea (AAD) and Clostridium difficile diarrhoea (CDD) in patients aged 65 ... | |||||||||||||
Medical condition: AAD is diarrhoea occurring in association with antibiotic treatment without an alternative cause. It occurs typically 2-8 weeks after exposure to antibiotics. The frequency of AAD varies markedly b... | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001573-10 | Sponsor Protocol Number: E2011HDinfection | Start Date*: 2012-01-24 | ||||||||||||||||
Sponsor Name:Hôpital Erasme | ||||||||||||||||||
Full Title: optimization of doses of broad spectrum B-lactames (ceftazidim and meropenem) and vancomycin in septic patient traeted with chronic hemodialysis. | ||||||||||||||||||
Medical condition: hemodialysis oligoanuria sepsis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-004239-29 | Sponsor Protocol Number: E2011OBINFECTION | Start Date*: 2011-10-04 | |||||||||||
Sponsor Name:Hopital Erasme | |||||||||||||
Full Title: what are the optimal doses of broad spectrum B-lactams to administer to obese patients if infected? | |||||||||||||
Medical condition: any patient with a BMI >= 30kg/m² and has a simple or severe infection. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019712-20 | Sponsor Protocol Number: DCSP1 | Start Date*: Information not available in EudraCT |
Sponsor Name:University of Oslo, Institute of Clinical Dentistry | ||
Full Title: D-CYCLOSERINE ENHANCEMENT OF EXPOSURE TREATMENT OF DENTALLY FEARFUL AND AVOIDANT CHILDREN. A PILOT STUDY | ||
Medical condition: Avoidance of dental care because of dental anxiety often result in reduced dental health and need for sedation or treatment in general anesthesia. Treatment of dental anxiety is time consuming and ... | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NO (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005399-15 | Sponsor Protocol Number: CEFFOS7 | Start Date*: 2010-03-10 |
Sponsor Name:Medizinische Universität Graz - Abteilung für Thorax- und Hyperbare Chirurgie | ||
Full Title: Penetration of Cubicin® and Fosfomycin® into skeletal muscle and subcutaneous adipose tissue of necrotizing soft tissue infections, measured by in-vivo microdialysis | ||
Medical condition: A group of adult male or female patients with documented necrotizing soft tissue infection who must be subjected to undergo intravenous antimicrobial therapy with broad spectrum antibiotics. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-004447-36 | Sponsor Protocol Number: ZonMw848015005 | Start Date*: 2017-06-23 |
Sponsor Name:Stichting Rotterdams Onderzoeksconsortium Kindergeneeskunde | ||
Full Title: INTRAVENOUS-TO-ORAL ANTIBIOTIC SWITCH THERAPY FOR SUSPECTED NEONATAL BACTERIAL INFECTIONS: CLINICAL EFFICACY, SAFETY AND COST-EFFECTIVENESS | ||
Medical condition: Neonatal probable bacterial infection | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005021-13 | Sponsor Protocol Number: MK-0991-044 | Start Date*: 2015-04-03 |
Sponsor Name:Merck & Co., Inc. | ||
Full Title: A Multicenter, Double-Blind, Randomized, Comparative Study to Evaluate the Safety, Tolerability, and Efficacy of Caspofungin Versus (Amphotericin B) Liposome for Injection as Empirical Therapy in P... | ||
Medical condition: Empirical Therapy in Pediatric Patients | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2013-000652-18 | Sponsor Protocol Number: E2013PK-OB-PTZ-MEM | Start Date*: 2013-03-19 | |||||||||||
Sponsor Name:Hopital Erasme | |||||||||||||
Full Title: Pharmacokinetics study of piperacillin-tazobactam and meropenem in obese patients | |||||||||||||
Medical condition: Obese patients with an infection treated by broad spectrum B-lactams. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000026-30 | Sponsor Protocol Number: ABR35278 | Start Date*: 2013-05-08 | |||||||||||
Sponsor Name:Academic medical centre | |||||||||||||
Full Title: Induction of Labour with a Foley catheter or oral Misoprostol at Term | |||||||||||||
Medical condition: Induction of labour at term | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
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: 2015-003633-10 | Sponsor Protocol Number: T150/2015 | Start Date*: 2016-03-03 | |||||||||||
Sponsor Name:Turku University Hospital | |||||||||||||
Full Title: Optimizing the antibiotic treatment of uncomplicated acute appendicitis: a prospective randomized multicenter study | |||||||||||||
Medical condition: Uncomplicated acute appendicitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022260-12 | Sponsor Protocol Number: 1947 | Start Date*: 2011-03-24 | |||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust | |||||||||||||
Full Title: A Phase II trial of broad spectrum antibiotic therapy for early stage chronic lymphocytic leukaemia. | |||||||||||||
Medical condition: Chronic Lymphocytic Leukaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008382-35 | Sponsor Protocol Number: AIFA - FARM07YPBW | Start Date*: 2010-04-08 | |||||||||||
Sponsor Name:Azienda Ospedaliera di Perugia | |||||||||||||
Full Title: Open , multicenter, randomized trial comparing two therapeutic approaches for the treatment of invasive fungal infections in neutropenic onco-hematologic patients.Empiric vs. ``presumptive`` (pree... | |||||||||||||
Medical condition: opportunistic fungal infections in neutropenic onco-hematologic patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001159-11 | Sponsor Protocol Number: POL7080-010 | Start Date*: 2019-02-08 | |||||||||||
Sponsor Name:Polyphor Ltd. | |||||||||||||
Full Title: A multicenter, open-label, sponsor-blinded, randomized, active-controlled, parallel group, pivotal study to evaluate the efficacy, safety, and tolerability of murepavadin given with ertapenem versu... | |||||||||||||
Medical condition: Nosocomial pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) FR (Prematurely Ended) LT (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000366-35 | Sponsor Protocol Number: RG_09-121 | Start Date*: 2011-09-15 | |||||||||||
Sponsor Name:University of Birmingham [...] | |||||||||||||
Full Title: Tackling Early Morbidity and Mortality in myeloma: assessing the benefit of antibiotic prophylaxis and its effect on healthcare associated infections | |||||||||||||
Medical condition: Infections during early symptomatic multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003933-27 | Sponsor Protocol Number: POL7080-011 | Start Date*: 2018-01-29 | |||||||||||
Sponsor Name:Polyphor Ltd. | |||||||||||||
Full Title: A multicenter, open-label, randomized, active-controlled, parallel group, pivotal study to investigate the efficacy, safety and tolerability, and pharmacokinetics of murepavadin combined with one a... | |||||||||||||
Medical condition: Ventilator-associated bacterial pneumonia (VABP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) EE (Prematurely Ended) ES (Prematurely Ended) FR (Prematurely Ended) HR (Completed) GR (Prematurely Ended) RO (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001496-36 | Sponsor Protocol Number: AMPISUL/AMOXICLAV-HD_V1.4 | Start Date*: 2013-07-19 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Innere Medizin I, Klinische abteilung für Infektionen und Tropenme | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Multiple-dose pharmacokinetics of ampicillin / sulbactam and amoxicillin / clavulanic acid during haemodialysis in longterm haemodialysis patients | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Suspected or proven bacterial infection requiring therapy with broad spectrum antibiotics | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: AT (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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