- Trials with a EudraCT protocol (43)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (7)
43 result(s) found for: Empirical treatment.
Displaying page 1 of 3.
EudraCT Number: 2012-003067-22 | Sponsor Protocol Number: PRISTINE | Start Date*: 2012-11-19 | |||||||||||
Sponsor Name:LUMC | |||||||||||||
Full Title: Pneumonia treated with rifampicine attenuates inflammation | |||||||||||||
Medical condition: Community acquired pneumonia CURB-65 class >1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2016-000078-39 | Sponsor Protocol Number: GEO-2014/01-HR | Start Date*: 2016-05-25 |
Sponsor Name:PLIVA Hrvatska d.o.o. | ||
Full Title: A prospective, multicentre, uncontrolled study of Geonistin vaginal tablets effectiveness with pharmacokinetic evaluation for unspecific and mixed vulvovaginal infections characterized by vaginal d... | ||
Medical condition: Unspecific and mixed vulvovaginal infections characterized by vaginal discharge. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: HR (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002569-37 | Sponsor Protocol Number: APHP180584 | Start Date*: 2020-05-13 |
Sponsor Name:Assistance Publique Hôpitaux de Paris | ||
Full Title: Empirical steroids and/or antifungals in immunocompromised patients with acute respiratory failure from undetermined etiology: a multicenter double-blind randomized controlled trial | ||
Medical condition: immunocompromised patients with acute respiratory failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2009-015800-25 | Sponsor Protocol Number: 810 | Start Date*: 2010-01-19 |
Sponsor Name:The Liverpool Heart & Chest Hospital NHS Trust | ||
Full Title: A pilot randomised control trial, in intensive care patients, comparing seven days versus two days treatment with empirical antibiotics to treat hospital acquired infection of unknown origin | ||
Medical condition: Healthcare associated infections This includes infections of the: • Skin and underneath the skin, including muscle - sometimes called ‘soft tissue’ • Urinary tract - including your kidneys or bladd... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001566-26 | Sponsor Protocol Number: BDG-ETHIC | Start Date*: 2017-01-11 | |||||||||||
Sponsor Name:AOU DI BOLOGNA POLICLINICO S.ORSOLA-MALPIGHI | |||||||||||||
Full Title: A B-D-GLUCAN DRIVEN ANTIFUNGAL STEWARDSHIP APPROACH TO MANAGE EMPIRICAL THERAPY IN PATIENTS AT VERY HIGH RISK FOR INVASIVE CANDIDIASIS: A RANDOMIZED CONTROLLED TRIAL | |||||||||||||
Medical condition: invasive candidiasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000574-69 | Sponsor Protocol Number: D9612L00076 | Start Date*: 2006-04-07 |
Sponsor Name:AstraZeneca A/S | ||
Full Title: Development of an algorithm for identification of responders to short term treatment with esomeprazol (Nexium) in primary care. | ||
Medical condition: acid related disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-023310-31 | Sponsor Protocol Number: MagicBullet/COLMER | Start Date*: 2011-02-07 | |||||||||||
Sponsor Name:Consorcio de apoyo a la Investigación Biomédica en Red (CAIBER) | |||||||||||||
Full Title: Ensayo clínico en fase IV aleatorizado, abierto, multicéntrico y de no inferioridad para comparar la seguridad y la eficacia de colistina iv. con meropenem iv. en el tratamiento de la neumonía asoc... | |||||||||||||
Medical condition: Neumonía asociada a ventilación mecánica | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) GR (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: 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: 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: 2010-020814-27 | Sponsor Protocol Number: 65091-06093 | Start Date*: 2012-05-10 | |||||||||||
Sponsor Name:EORTC | |||||||||||||
Full Title: Empirical versus pre-emptive (diagnostic-driven) antifungal therapy of patients treated for haematological malignancies or receiving an allogeneic stem cell transplant. A therapeutic open label pha... | |||||||||||||
Medical condition: Invasive fungal infection in patients with hematological malignancies. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) BE (Completed) CZ (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001549-32 | Sponsor Protocol Number: Caspofungin vs Amfotericina | Start Date*: 2006-03-01 | |||||||||||
Sponsor Name:A.I.E.O.P. - ASSOCIAZIONE ITALIANA EMATOLOGIA ONCOLOGIA PEDIATRICA | |||||||||||||
Full Title: Prospectic, multicentric, randomized, controlled trial for the evaluation of efficacy of Caspofungin vs Amfotericina B liposomiale for the empirical treatment of the FUO in children neutropenic for... | |||||||||||||
Medical condition: Neutropenia (neutrophil count <500/mm3 for at least 10 days persistent fever for at least 72-96 hours, refrectory to the traetment with wide spectrum antibiotic appropriate for high risk pa... | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005032-34 | Sponsor Protocol Number: MK-0991-058 | Start Date*: 2015-02-27 |
Sponsor Name:Merck & Co., Inc. | ||
Full Title: A Multicenter, Sequential-Panel, Open-Label, Noncomparative Study to Investigate the Safety, Tolerability, and Pharmacokinetics of Caspofungin Acetate in Neonates and Infants Less Than 3 Months of ... | ||
Medical condition: Empirical therapy for fungal infections | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2014-003558-15 | Sponsor Protocol Number: M14-197 | Start Date*: 2015-07-14 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Phase 2 Study to Investigate the Safety, Tolerability and Efficacy of ABT-122 in Subjects with Active Psoriatic Arthritis Who Have an Inadequate Response to Methotrexate | |||||||||||||
Medical condition: Psoriatic Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LV (Completed) HU (Completed) CZ (Completed) ES (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001108-47 | Sponsor Protocol Number: BARIFER | Start Date*: 2016-05-29 |
Sponsor Name:Fundació Hospital Universitari Vall Hebron-Institut de Recerca (VHIR) | ||
Full Title: Impact of eradication of asymptomatic bacteriuria on reducing the incidence of early infection in patients with periprosthetic femoral fractures requiring hip hemiarthroplasty | ||
Medical condition: Early infection in patients with periprosthetic femoral fracture | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-001840-83 | Sponsor Protocol Number: SAGA | Start Date*: 2022-04-26 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: Short-course aminoglycosides as adjunctive treatment in adults with sepsis | ||
Medical condition: Patients admitted with sepsis of unknown origin, suspected urinary origin or suspected abdominal origin | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016476-67 | Sponsor Protocol Number: 780/09 | Start Date*: 2009-03-23 | ||||||||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | ||||||||||||||||||
Full Title: treatment of healthcare-associated pneumonia: a prospective, multicenter study | ||||||||||||||||||
Medical condition: Pneumonia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002800-40 | Sponsor Protocol Number: A1501073 | Start Date*: 2006-02-09 | |||||||||||
Sponsor Name:Pfizer Ltd | |||||||||||||
Full Title: Prospective, Open-label, Comparative, Multicenter Study of Voriconazole Compared to Itraconazole for the Primary Prophylaxis of Invasive Fungal Infections (IFI) in Subjects with Allogeneic Hematopo... | |||||||||||||
Medical condition: Prophylaxis against invasive fungal infection following allogeneic hematopoietic stem cell transplantation. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) CZ (Completed) ES (Completed) PT (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001759-22 | Sponsor Protocol Number: PGX401-11 | Start Date*: 2015-07-24 | |||||||||||||||||||||||||||||||
Sponsor Name:Laboratoire Innotech International | |||||||||||||||||||||||||||||||||
Full Title: Assessment of the efficacy of POLYGYNAX® in the empirical treatment of infectious vaginitis International, multicentre, randomised, double-blind, parallel group study, comparative versus miconazole | |||||||||||||||||||||||||||||||||
Medical condition: Patients presenting with abnormal vaginal discharge associated with other vaginal symptoms (i.e. vaginal burning and/or vaginal irritation and/or vaginal pain) clinically evoking infectious vaginit... | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) CZ (Completed) SK (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
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