- Trials with a EudraCT protocol (29)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
29 result(s) found for: Antimicrobials.
Displaying page 1 of 2.
EudraCT Number: 2018-004880-29 | Sponsor Protocol Number: HUB-INF-RADICAP | Start Date*: 2019-10-02 | |||||||||||
Sponsor Name:Dr. Jordi Carratalà Fernández (Servicio de Enfermedades Infecciosas) del Hospital Universitario de Bellvitge | |||||||||||||
Full Title: Phase IV randomized, controlled, open and multicentre clinical trial with two parallel groups, to assess the impact of integral molecular tests in the antimicrobial use in community-acquired pneumo... | |||||||||||||
Medical condition: Community-acquired pneumonia (CAP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001376-38 | Sponsor Protocol Number: LOCKIA | Start Date*: 2019-08-13 |
Sponsor Name:María Dolores Sousa Regueiro | ||
Full Title: Antimicrobials Local Administration for Intraabdominal Abscesses Treatment: Controlled, Randomized, Open, Parallel Groups, Clinical Trial | ||
Medical condition: Intra-abdominal abscesses | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001769-35 | Sponsor Protocol Number: OYS042020. | Start Date*: Information not available in EudraCT |
Sponsor Name:Oulu University Hopsital | ||
Full Title: Preventing urinary tract infections in infants and young children with probiotic E. coli Nissle: FinNiss- trial | ||
Medical condition: Urinary tract infection | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: FI (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004736-51 | Sponsor Protocol Number: nov 2005 | Start Date*: 2006-09-26 |
Sponsor Name:Prof V Lund | ||
Full Title: Double-blind randomized placebo-controlled multinational, multicentre-trial on prolonged macrolide treatment in patients with moderate/severe chronic rhinosinusitis | ||
Medical condition: chronic rhinitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001728-30 | Sponsor Protocol Number: MPEX-204 | Start Date*: 2008-08-26 | ||||||||||||||||
Sponsor Name:Mpex Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Phase 2, Multi-center, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety, Tolerability and Efficacy of Three Dosage Regimens of MP- 376 Solution for Inhalation Given for 2... | ||||||||||||||||||
Medical condition: Pseudomonas aeruginosa infection in patients suffering from stable Cystic Fibrosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-001062-14 | Sponsor Protocol Number: MEC 04/265 | Start Date*: 2006-02-23 |
Sponsor Name:prof W.J. Fokkens, academic medical center | ||
Full Title: MACS Macrolides in chronic rhinosinusitis Double-blind, randomized, placebo-controlled, multinational, multicenter-trial on prolonged macrolide treatment in patients with moderate/ severe chronic... | ||
Medical condition: Chronic rhinosinusitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002011-33 | Sponsor Protocol Number: PROGRESS | Start Date*: 2017-08-28 | |||||||||||
Sponsor Name:Hellenic Institute for the Study of Sepsis | |||||||||||||
Full Title: A RANDOMIZED PROSPECTIVE CLINICAL TRIAL TO ASSESS THE ROLE OF PROCALCITONIN-GUIDED ANTIMICROBIAL THERAPY TO REDUCE LONG-TERM INFECTIONS SEQUELAE | |||||||||||||
Medical condition: USE OF PROCALCITONIN IN EARLY STOP OF ANTIBIOTICS TO AVOID LONG-TERM CONSEQUENCES | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022150-16 | Sponsor Protocol Number: Moxifloxacin Sepsis PEG | Start Date*: 2011-01-27 |
Sponsor Name:Medizinische Universität Wien, Univ.Klinik f.klinische Pharmakologie | ||
Full Title: Determination of Moxifloxacin concentrations in interstitial space fluid of muscle and subcutis in septic patients including a pilot phase | ||
Medical condition: To evaluate feasibility of Moxifloxacin determination in septic patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2018-001505-90 | Sponsor Protocol Number: 18CH049 | Start Date*: 2018-10-01 | ||||||||||||||||
Sponsor Name:CHU de Saint Etienne | ||||||||||||||||||
Full Title: Decolonization of patients carrying S. aureus before cardiac surgery: study of the risk factors associated with failure | ||||||||||||||||||
Medical condition: Decolonization of S. aureus nasal carriers before cardiac surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001124-19 | Sponsor Protocol Number: 04-24 | Start Date*: 2013-09-25 | |||||||||||
Sponsor Name:Onconova Therapeutics, Inc. | |||||||||||||
Full Title: Phase IIIB, Open-label, Multi-Center Study of the Efficacy and Safety of rigosertib Administered as 72-hour Continuous Intravenous Infusions in Patients with Myelodysplastic Syndrome with Excess Bl... | |||||||||||||
Medical condition: Myelodysplastic Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) SE (Completed) DK (Completed) ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000599-18 | Sponsor Protocol Number: P903-09 | Start Date*: 2008-03-25 | |||||||||||
Sponsor Name:Cerexa, Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Comparative Study to Evaluate the Safety and Efficacy of Ceftaroline versus Ceftriaxone in the Treatment of Adult Subjects with Community-Acquired ... | |||||||||||||
Medical condition: Adult Subjects with Community-Acquired Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) DE (Completed) HU (Completed) AT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002202-31 | Sponsor Protocol Number: POL7080-002 | Start Date*: 2013-09-11 |
Sponsor Name:Polyphor Ltd. | ||
Full Title: A phase II, open-label, multi-center study to assess the tolerance, safety, efficacy and pharmacokinetics/pharmacodynamics (PK/PD) of POL7080 in the treatment of patients with acute exacerbation of... | ||
Medical condition: Acute exacerbation of non-cystic fibrosis bronchiectasis due to Pseudomonas aeruginosa infection. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Prematurely Ended) DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-006096-37 | Sponsor Protocol Number: BAY 12-8039/11980 | Start Date*: 2008-05-09 | |||||||||||
Sponsor Name:Bayer HealthCare AG, Leverkusen, Germany | |||||||||||||
Full Title: A prospective, multinational, multicenter, randomized, double-blind, double-dummy, controlled study comparing the efficacy and safety of moxifloxacin to that of amoxicillin-clavulanic acid for the ... | |||||||||||||
Medical condition: acute exacerbation of chronic bronchitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Completed) IE (Completed) BE (Completed) DE (Completed) ES (Completed) PT (Completed) GR (Completed) LT (Completed) LV (Completed) IT (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005805-25 | Sponsor Protocol Number: M19-771 | Start Date*: 2021-11-10 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Phase 2 Study of Galicaftor/Navocaftor/ABBV-119 Combination Therapy in Subjects with Cystic Fibrosis Who Are Homozygous or Heterozygous for the F508del Mutation. | |||||||||||||
Medical condition: Cystic Fibrosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) HU (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BG (Completed) GR (Ongoing) IT (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000598-41 | Sponsor Protocol Number: P903-08 A4 | Start Date*: 2007-11-22 | |||||||||||
Sponsor Name:Cerexa, Inc. | |||||||||||||
Full Title: "A Phase 3, Multicenter, Randomized, Double-blind, Comparative Study to Evaluate the Safety and Efficacy of Ceftaroline versus Ceftriaxone, with Adjunctive Clarithromycin, in the Treatment of Adult... | |||||||||||||
Medical condition: Adults Subjects with Community-Acquired Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) ES (Completed) AT (Completed) LT (Completed) EE (Completed) SK (Completed) BG (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000775-32 | Sponsor Protocol Number: AB.OH.2018 | Start Date*: 2018-06-05 | |||||||||||
Sponsor Name:Vall d'Hebron Institut de Recerca | |||||||||||||
Full Title: Phase IV, randomized, open, parallel groups clinical trial for evaluating the early Stop of antibiotic Treatment in febrile neutropenic Oncohematological Paediatric patients. | |||||||||||||
Medical condition: Febrile neutrophenia in oncohematological pediatric patients. | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005283-47 | Sponsor Protocol Number: P903-07 | Start Date*: 2006-12-29 | |||||||||||
Sponsor Name:Cerexa, Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Comparative Study to Evaluate the Safety and Efficacy of Ceftaroline Versus Vancomycin plus Aztreonam in Adult Subjects with Complicated Skin and ... | |||||||||||||
Medical condition: Complicated Skin and Skin Structure Infections (cSSSI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) GB (Completed) DE (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005332-25 | Sponsor Protocol Number: P903-06 | Start Date*: 2007-03-16 | |||||||||||
Sponsor Name:Cerexa, Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Comparative Study to Evaluate the Safety and Efficacy of Ceftaroline Versus Vancomycin plus Aztreonam in Adult Subjects with Complicated Skin and ... | |||||||||||||
Medical condition: Complicated Skin and Skin Structure Infections (cSSSI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002366-40 | Sponsor Protocol Number: 13.0095 | Start Date*: 2013-07-19 |
Sponsor Name:St George’s, University of London | ||
Full Title: Neonatal and Paediatric Pharmacokinetics of Antimicrobials study | ||
Medical condition: The study is not restricted to any specific condition. The study population will include children (aged under 16 years) admitted to hospital and routinely prescribed one of the study penicillins ac... | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
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