- Trials with a EudraCT protocol (1,302)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,302 result(s) found for: Bacterial Infections AND Bacterial Infections..
Displaying page 2 of 66.
| 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: 2015-002218-60 | Sponsor Protocol Number: 0101 | Start Date*: 2015-07-03 | |||||||||||
| Sponsor Name:Theravance Biopharma Antibiotics, Inc. | |||||||||||||
| Full Title: An Open-Label Study of the Pharmacokinetics of a Single Dose of Telavancin in Pediatric Subjects Aged 1 to 17 Years | |||||||||||||
| Medical condition: Gram-Positive Bacterial Infections | |||||||||||||
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| Population Age: 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: 2010-024117-31 | Sponsor Protocol Number: APROBECHA | Start Date*: 2011-10-27 | |||||||||||
| Sponsor Name:Instituto Científico y Tecnológico de Navarra | |||||||||||||
| Full Title: Estudio de la eficacia de la administración prolongada de antibióticos betalactámicos frente a la administración intermitente en el tratamiento de la infección causada por microorganismo sensibles ... | |||||||||||||
| Medical condition: Infección microbiana | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002489-15 | Sponsor Protocol Number: 380119 | Start Date*: 2021-03-23 | |||||||||||
| Sponsor Name:Medinova AG | |||||||||||||
| Full Title: Comparative study of the efficacy and safety of vaginally applied Dequalinium Chloride (10 mg) and orally applied Metronidazole (2 x 500 mg) in the treatment of bacterial vaginosis | |||||||||||||
| Medical condition: Bacterial vaginosis | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: CZ (Prematurely Ended) SK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-004424-38 | Sponsor Protocol Number: SUTRICA | Start Date*: 2013-01-29 | ||||||||||||||||
| Sponsor Name:Department of Haematology, Aalborg University Hospital | ||||||||||||||||||
| Full Title: A randomized, open-label phase III study of Clarithromycin, Sulfamethoxa-zole/Trimethoprim or observation in combination with standard therapy in patients with newly diagnosed multiple myeloma | ||||||||||||||||||
| Medical condition: Multiple myeloma | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-001663-23 | Sponsor Protocol Number: CAP01-2013 | Start Date*: 2013-09-02 | |||||||||||
| Sponsor Name:FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO MILANO | |||||||||||||
| Full Title: Clinical and immunomodulatory effects of antibiotic therapy + pidotimod versus antibiotic therapy alone in patients with community-acquired pneumonia (CAP) | |||||||||||||
| Medical condition: Community acquired pneumonia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001019-95 | Sponsor Protocol Number: COLIMICINA | Start Date*: 2021-05-31 | |||||||||||
| Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
| Full Title: Pharmacokinetic/pharmacodynamic aspects of colistin intravenous administration in critically ill patients suffering from hospital infections caused by multi-antibiotic-resistant germs and receiving... | |||||||||||||
| Medical condition: Critically ill patients suffering from hospital infections caused by multi-antibiotic-resistant germs and receiving continuous renal replacement therapy. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-002868-31 | Sponsor Protocol Number: 68Ga-DFO-B-I/IIa | Start Date*: 2020-10-23 |
| Sponsor Name:Medizinische Universität Innsbruck | ||
| Full Title: A Phase I/IIa study to evaluate safety, biodistribution, dosimetry and preliminary diagnostic performance of [68Ga]Ga-Deferoxamine for PET imaging in patients with bacterial infections | ||
| Medical condition: Upper/lower respiratory tract bacterial infections or orthopaedic bacterial infections | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-000419-15 | Sponsor Protocol Number: DUR001-303 | Start Date*: 2014-07-28 | |||||||||||
| Sponsor Name:Durata Therapeutics International B.V. | |||||||||||||
| Full Title: A Phase 3b, Double-Blind, Multicenter, Randomized Study to Compare the Efficacy and Safety of Single Dose Dalbavancin to a Two Dose Regimen of Dalbavancin for the Treatment of Acute Bacterial Skin ... | |||||||||||||
| Medical condition: Acute Bacterial Skin and Skin Structure Infections | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: LV (Completed) EE (Completed) HU (Completed) BG (Completed) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003356-51 | Sponsor Protocol Number: ZEL001 | Start Date*: 2015-10-15 | |||||||||||
| Sponsor Name:Zelmic AB | |||||||||||||
| Full Title: A single-centre, open-label, single-arm, Phase I/II study to investigate the effect of a hydrogen peroxide foam on clinical signs and symptoms and the vaginal flora in patients with bacterial vagin... | |||||||||||||
| Medical condition: Bacterial vaginosis | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-004483-19 | Sponsor Protocol Number: RRK5908 | Start Date*: 2017-09-09 | |||||||||||
| Sponsor Name:University Hospitals Birmingham NHS Foundation Trust | |||||||||||||
| Full Title: A randomised controlled trial to assess the clinical and cost effectiveness of topical lactic acid gel for treating second and subsequent episodes of bacterial vaginosis | |||||||||||||
| Medical condition: Bacterial Vaginosis | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002644-40 | Sponsor Protocol Number: B3451002 | Start Date*: 2015-05-27 | ||||||||||||||||
| Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017 | ||||||||||||||||||
| Full Title: A Phase 2B, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of Staphylococcus Aureus 4-Antigen Vaccine (SA4Ag) in Adults Undergoing Elective Posterior Instrum... | ||||||||||||||||||
| Medical condition: Prophylaxis for prevention of Post-operative S. aureus infection | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) HU (Completed) AT (Prematurely Ended) SE (Prematurely Ended) BG (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-002729-39 | Sponsor Protocol Number: C-07-40 | Start Date*: 2017-11-07 | |||||||||||
| Sponsor Name:Alcon Research Ltd | |||||||||||||
| Full Title: An Evaluation of the Safety and Efficacy of Moxifloxacin AF Ophthalmic Solution 0.5% for the Treatment of Bacterial Conjunctivitis in the USA | |||||||||||||
| Medical condition: Bacterial conjunctivitis | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002730-23 | Sponsor Protocol Number: C-04-38 | Start Date*: 2017-11-07 | |||||||||||
| Sponsor Name:Alcon Research Ltd | |||||||||||||
| Full Title: An Evaluation of the Safety and Efficacy of Moxifloxacin AF Ophthalmic Solution 0.5% for the Treatment of Bacterial Conjunctivitis in the USA | |||||||||||||
| Medical condition: Bacterial conjunctivitis | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002727-24 | Sponsor Protocol Number: C-10-051 | Start Date*: 2017-11-07 | |||||||||||
| Sponsor Name:Alcon Research | |||||||||||||
| Full Title: An Evaluation of the Safety and Efficacy of Moxifloxacin Ophthalmic Solution 0.5% Versus Ofloxacin Ophthalmic Solution 0.3% in the Treatment of Bacterial Conjunctivitis in Chinese Patients | |||||||||||||
| Medical condition: bacterial conjunctivitis | |||||||||||||
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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: 2017-004544-38 | Sponsor Protocol Number: C3601009 | Start Date*: 2020-07-03 | |||||||||||
| Sponsor Name:Pfizer Inc. | |||||||||||||
| Full Title: A PROSPECTIVE, RANDOMIZED, OPEN-LABEL, COMPARATIVE STUDY TO ASSESS THE EFFICACY, SAFETY AND TOLERABILITY OF AZTREONAM-AVIBACTAM (ATM-AVI) AND BEST AVAILABLE THERAPY FOR THE TREATMENT OF SERIOUS INF... | |||||||||||||
| Medical condition: SERIOUS INFECTIONS DUE TO MULTI-DRUG RESISTANT GRAM- NEGATIVE BACTERIA PRODUCING METALLO-Β-LACTAMASE (MBL) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Prematurely Ended) RO (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-002203-18 | Sponsor Protocol Number: P903-31 | Start Date*: 2012-07-18 | ||||||||||||||||||||||||||
| Sponsor Name:Cerexa, Inc. (subsidary of Forest Laboratories) | ||||||||||||||||||||||||||||
| Full Title: A Multicenter, Randomized, Observer-Blinded, Active-Controlled Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of Ceftaroline Versus Ceftriaxone in Pediatric Subjects With... | ||||||||||||||||||||||||||||
| Medical condition: Community-acquired Bacterial Pneumonia | ||||||||||||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: Outside EU/EEA HU (Completed) GR (Completed) ES (Completed) PL (Completed) BG (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2014-000694-39 | Sponsor Protocol Number: SPL7013-018 | Start Date*: 2014-10-22 | |||||||||||
| Sponsor Name:Starpharma Pty Ltd | |||||||||||||
| Full Title: A phase 3, double-blind, multicentre, randomised, placebo-controlled study to determine the efficacy and safety of SPL7013 Gel (VivaGel®) to prevent the recurrence of bacterial vaginosis | |||||||||||||
| Medical condition: recurrent bacterial vaginosis | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: CZ (Completed) GB (Completed) HU (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002926-35 | Sponsor Protocol Number: 080716CT | Start Date*: 2017-01-16 | |||||||||||
| Sponsor Name:Alder Hey Children's Foundation NHS Trust | |||||||||||||
| Full Title: Pharmacokinetics of post-operative Cefuroxime in infants undergoing cardiac surgery | |||||||||||||
| Medical condition: post operative paediatric cardiac patients | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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