- Trials with a EudraCT protocol (996)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
996 result(s) found for: Bacterial disease.
Displaying page 1 of 50.
EudraCT Number: 2008-001426-14 | Sponsor Protocol Number: Preda | Start Date*: 2009-03-02 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PROVINCIALE DI LECCO | |||||||||||||
Full Title: a probiotic for the prevention of diarrhoea associated with antibiotics | |||||||||||||
Medical condition: Diarrheoa from AAD and CD | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001321-25 | Sponsor Protocol Number: 101596 | Start Date*: 2004-05-19 | |||||||||||
Sponsor Name:WYETH LEDERLE | |||||||||||||
Full Title: A prospective, open label, monocenter trial to evaluate the interaction between the Platelia Aspergillus ELISA test and the administration of piperacillin/tazobactam. | |||||||||||||
Medical condition: Evaluation of interference between platelia aspergillus ELISA TEST and administration of PIPERACILLIN/TAZOBACTAM. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001901-81 | Sponsor Protocol Number: AISAR-01-04 | Start Date*: 2004-07-23 | |||||||||||
Sponsor Name:AISAR ASSOCIAZIONE ITALIANA PER LO STUDIO DEGLI ANTIMICROBICI E DELLE RESISTENZE | |||||||||||||
Full Title: Efficacy and tollerability of thiamphenicol glycinate acetylcysteinate, given in sequential therapy sistematic and aerosol or by aerosol in the treatment of hight respiratory tract acute infectio... | |||||||||||||
Medical condition: terapia sequenziale sistemica ed aerosol delle infezioni acute e/o subacute/ricorrenti delle alte vie respiratorie | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014387-20 | Sponsor Protocol Number: DORI-PED-1003 | Start Date*: 2009-10-23 | |||||||||||
Sponsor Name:Janssen-Cilag International NV, Turnhoutseweg 30, 2340 Beerse, Belgium | |||||||||||||
Full Title: An Open-Label Study to Evaluate the Single-Dose Pharmacokinetics, Safety, and Tolerability of Doripenem in Infants (Term and Preterm), Less Than 12 Weeks Chronological Age Protocol DORI-PED-1003;... | |||||||||||||
Medical condition: hospitalized but medically stable infants (term and preterm), <12 weeks CA, who have documented, presumed to have, or are at risk for bacterial infection(s) and are undergoing treatment with i.v. a... | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000415-32 | Sponsor Protocol Number: DAL-PK-02 | Start Date*: 2022-06-07 | |||||||||||
Sponsor Name:Allergan | |||||||||||||
Full Title: Pharmacokinetics of a Single-Dose of Dalbavancin in Preterm Neonates to Infants Ages 3 Months With Suspected or Confirmed Bacterial Infection | |||||||||||||
Medical condition: Bacterial Infection in hospitalized children | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005415-26 | Sponsor Protocol Number: TMC-ORI-11-01 | Start Date*: 2015-03-19 | |||||||||||||||||||||
Sponsor Name:Melinta Therapeutics | |||||||||||||||||||||||
Full Title: An Open label, Dose-finding, Pharmacokinetics, Safety, and Tolerability Study of Oritavancin Single Dose Infusion in Pediatric Subjects Less Than 18 Years of Age with Suspected or Confirmed Bacteri... | |||||||||||||||||||||||
Medical condition: Gram positive bacterial infection | |||||||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003914-42 | Sponsor Protocol Number: CEFTAROLINE_RRT | Start Date*: 2013-11-06 | |||||||||||
Sponsor Name:Medizinische Universität Wien, Univ.-Klinik für Innere Medizin I, Klinische Abteilung für Infetionen und Tropenmedizin | |||||||||||||
Full Title: Multiple-dose Pharmacokinetics of Ceftaroline during continuous and intermittent renal replacement therapy in patients requiring renal replacement therapy | |||||||||||||
Medical condition: Bacterial infection in patients recieving renal replacement therapy | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004628-23 | Sponsor Protocol Number: M000507_6004 | Start Date*: 2015-03-17 | |||||||||||
Sponsor Name:Sanofi | |||||||||||||
Full Title: Comparison of Teicoplanin and Vancomycin in Terms of Efficacy and Side Effect Profile During Initial Antibiotic Treatment of Febrile Neutropenic Patients at High Risk For Gram-Positive Infection: M... | |||||||||||||
Medical condition: Neutropenic and febrile patients with hematological or solid tumors, who are at high risk for gram-positive bacterial infection. | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001900-13 | Sponsor Protocol Number: D4280C00014 | Start Date*: 2013-06-05 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase I Study to Assess the Pharmacokinetics, Safety and Tolerability of a Single Dose of Ceftazidime-Avibactam (CAZ-AVI) in Children From 3 Months of Age to <18 Years Who Are Receiving Systemic ... | |||||||||||||
Medical condition: hospitalized pediatric patients receiving systemic antibiotic therapy for suspected or confirmed infection. | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002148-95 | Sponsor Protocol Number: SHORTEN | Start Date*: 2014-05-21 | |||||||||||
Sponsor Name:Fundación Pública Andaluza para la Gestión en Salud de Sevilla (FISEVI) | |||||||||||||
Full Title: Optimal duration of the antimicribial treatment for bloodstream infections produced by Enterobacteriaceae. Clinical trial "SHORTEN". | |||||||||||||
Medical condition: Adult patients with bloodstream infections produced by Enterobacteriaceae. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
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: 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: 2015-004306-42 | Sponsor Protocol Number: 2016-1 | Start Date*: 2016-01-27 | |||||||||||
Sponsor Name:Stomatološka klinika UKC, Ljubljana | |||||||||||||
Full Title: Comparison of the efficacy of treatment of chronic periodontitis with scaling and root-planning alone or in combination with azithromycin - a prospective, double blind, randomised clinical trial | |||||||||||||
Medical condition: Number of remaining deep pockets after treatment of patients with chornic periodontitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006210-14 | Sponsor Protocol Number: GIMEMA01 | Start Date*: 2007-07-12 | |||||||||||
Sponsor Name:UNIVERSITA' DEGLI STUDI DI PERUGIA | |||||||||||||
Full Title: PIPERACILLIN/TAZOBACTAM PLUS TIGECYCLINE VS. PIPERACILLIN/TAZOBACTAM ALONE AS EMPIRICAL THERAPY FOR FEBRILE NEUTROPENIC CANCER PATIENTS : A PROSPECTIVE, RANDOMISED, MULTI-CENTRE, STUDY. | |||||||||||||
Medical condition: Neutropenic, febrile cancer patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003227-11 | Sponsor Protocol Number: DUR001-106 | Start Date*: 2014-11-28 | ||||||||||||||||
Sponsor Name:Durata Therapeutics International B.V. | ||||||||||||||||||
Full Title: PHASE 1, OPEN LABEL, SINGLE DOSE STUDY TO INVESTIGATE THE PHARMACOKINETICS, SAFETY AND TOLERABILITY OF DALBAVANCIN IN HOSPITALIZED CHILDREN AGED 3 MONTHS TO 11 YEARS RECEIVING STANDARD INTRAVENOUS ... | ||||||||||||||||||
Medical condition: Bacterial Infection in hospitalized children | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: EE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000656-99 | Sponsor Protocol Number: REMPEX-507 | Start Date*: 2023-09-28 | ||||||||||||||||||||||||||
Sponsor Name:Rempex Pharmaceuticals-Melinta Therapeutics | ||||||||||||||||||||||||||||
Full Title: An Open label, Dose-finding, Pharmacokinetics, Safety, and Tolerability Study of a Single Dose Infusion of VABOMERE® (Meropenem-Vaborbactam) in Pediatric Subjects From Birth to Less Than 18 Years o... | ||||||||||||||||||||||||||||
Medical condition: Suspected or confirmed negative bacterial infection | ||||||||||||||||||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002386-38 | Sponsor Protocol Number: CLVS100VER | Start Date*: 2011-09-30 | |||||||||||
Sponsor Name:VERISFIELD (UK) LTD | |||||||||||||
Full Title: | |||||||||||||
Medical condition: Bacterial Vaginosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001858-33 | Sponsor Protocol Number: SURVIC_STUDY | Start Date*: 2023-03-24 | ||||||||||||||||
Sponsor Name:IDIBAPS (Institit d'Investigacions Biomèdiques August Pi I Sunyer) | ||||||||||||||||||
Full Title: Randomized controlled trial comparing conventional antibiotic strategies versus regimens guided by epidemiological surveillance in infected patients with cirrhosis. | ||||||||||||||||||
Medical condition: Hospitalized patients with decompensated cirrhosis, diagnosed with bacterial infection evolution lasting for 48 hours or less. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
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) |
EudraCT Number: 2017-000717-24 | Sponsor Protocol Number: 230390 | Start Date*: 2017-08-24 | |||||||||||||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||||||||||||
Full Title: Concentration of piperacillin in plasma and subcutis in patients on crrt treatment | |||||||||||||||||||||||
Medical condition: infections reloated to CRRT | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
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