- Trials with a EudraCT protocol (67)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
67 result(s) found for: Leukocytosis.
Displaying page 1 of 4.
EudraCT Number: 2011-004566-14 | Sponsor Protocol Number: SanteonCAP | Start Date*: 2012-01-09 |
Sponsor Name: | ||
Full Title: Santeon-CAP study Dexamethasone in community-acquired pneumonia. | ||
Medical condition: Patients with a community-acquired pneumonia who are admitted to the hospital. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005633-10 | Sponsor Protocol Number: DORI INI 2002 | Start Date*: 2008-01-24 | ||||||||||||||||
Sponsor Name:ORTHO MCNEIL JANSSEN SCIENTIFIC AFFAIRS, LLC | ||||||||||||||||||
Full Title: A Phase 2, Open-Label, Non-Comparative Study of Doripenem in the Treatment of Nosocomial and Ventilator-Associated Pneumonia in Hospitals where Pseudomonas aeruginosa may be a Prevalent Pathogen. | ||||||||||||||||||
Medical condition: Nosocomial and Ventilator-Associated Pneumonia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-002708-28 | Sponsor Protocol Number: REDIV/002/17 | Start Date*: 2018-02-23 | |||||||||||
Sponsor Name:Alfasigma S.p.a | |||||||||||||
Full Title: Rifaximin delayed release (400 mg tablet) for the prevention of recurrent acute diverticulitis and diverticular complications. A phase II, multicenter, double-blind, placebo-controlled, randomized ... | |||||||||||||
Medical condition: Prevention of recurrent acute diverticulitis and diverticular complications | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) DE (Completed) HU (Completed) FR (Completed) NL (Completed) GB (GB - no longer in EU/EEA) PT (Completed) IT (Prematurely Ended) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004886-33 | Sponsor Protocol Number: A06-269 | Start Date*: 2007-06-05 |
Sponsor Name:University of Athens, Medical school | ||
Full Title: A DOUBLE-BLIND RANDOMIZED PLACEBO-CONTROLLED CLINICAL TRIAL OF THE SAFETY AND IMMUNOMODULATORY THERAPY FOR THE MANAGEMENT OF SEPSIS | ||
Medical condition: septic syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004824-19 | Sponsor Protocol Number: ML21206 | Start Date*: 2008-08-08 |
Sponsor Name:Roche Austria GmbH | ||
Full Title: Bevacizumab in Chronic Lymphocytic Leukemia: a proof of concept study | ||
Medical condition: Chronic Lymphocytic Leukemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2004-001730-17 | Sponsor Protocol Number: BAP00248/307 | Start Date*: 2004-09-16 | |||||||||||
Sponsor Name:Johnson & Johnson Pharmaceutical Research & Development, L.L.C. | |||||||||||||
Full Title: A Phase 3, Randomized Double-Blind Study of Ceftobiprole Medocaril Versus Linezolid Plus Ceftazidime in the Treatment of Nosocomial Pneumonia | |||||||||||||
Medical condition: Nosocomial Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) LV (Completed) HU (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001965-98 | Sponsor Protocol Number: PGFN-001 | Start Date*: 2017-01-10 | |||||||||||
Sponsor Name:Prolong Pharmaceuticals, LLC | |||||||||||||
Full Title: A randomized and open-label dose-finding, phase 2, efficacy, safety, and pharmacokinetic study of once-per-cycle prophylactic injections of ANF-RHO™ versus pegfilgrastim (Neulasta®) in non-metastat... | |||||||||||||
Medical condition: chemotherapy-induced neutropenia (CIN) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000835-84 | Sponsor Protocol Number: 30982081-CAP-3001 | Start Date*: 2006-10-10 | |||||||||||
Sponsor Name:Jansen-Cilag International N.V. | |||||||||||||
Full Title: Randomized, Double-Blind, Multicenter Study of Ceftobiprole Medocaril Versus Ceftriaxone with/without Linezolid in Treatment of Subjects Hospitalized With Community-Acquired Pneumonia | |||||||||||||
Medical condition: Hospitalized community acquired pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LT (Completed) HU (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004174-24 | Sponsor Protocol Number: BAP00248 | Start Date*: 2006-08-24 |
Sponsor Name:Johnson&Johnson Pharmaceutical Research&Development, L.L.C. | ||
Full Title: A Phase 3 Randomized, Double-Blind Study of Ceftobiprole Medocaril versus Linezolid Plus Ceftazidime in the Treatment of Nosocomial Pneumonia | ||
Medical condition: Hospital-Acquired or Nosocomial Pneumonia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-002634-35 | Sponsor Protocol Number: MHH-MW-01 | Start Date*: 2005-08-25 |
Sponsor Name:Klinik für Allgemein-, Viszeral- und Transplantationschirurgie, Medizinische Hochschule Hannover | ||
Full Title: Single centre, prospective, comparative, open-label, randomised study to evaluate the efficacy and tolerability of the combination of Moxifloxacin plus Metronidazole versus Piperacillin/Tazobactam ... | ||
Medical condition: The patients to be treated present with intra-abdominal abscesses (clinical or radiological or sonomorphological diagnosis) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-005144-14 | Sponsor Protocol Number: 01-CARDIONIDO | Start Date*: 2018-04-12 |
Sponsor Name:Dr. Forteza Gil | ||
Full Title: Comparative study of two types of cardioplegia during cardiac surgery in the adult patient | ||
Medical condition: Cardiac surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003917-83 | Sponsor Protocol Number: CHAVANET-BASILEA-2016 | Start Date*: 2017-08-16 | |||||||||||
Sponsor Name:CHU de DIJON | |||||||||||||
Full Title: Open and exploratory trial to investigate the pharmacokinetic of ceftobiprole medocaril in patients with CSF device | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001406-17 | Sponsor Protocol Number: 48009 | Start Date*: 2015-01-21 |
Sponsor Name:Erasmus MC | ||
Full Title: Ventilator Associated Pneumonia: addition of Tobramycin Inhalation antibiotic treatment to standard IV antibiotic treatment | ||
Medical condition: ICU patients with ventilator-associated pneumonia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002612-25 | Sponsor Protocol Number: versie 2 | Start Date*: 2007-09-14 | |||||||||||
Sponsor Name:St. Antonius Hospital | |||||||||||||
Full Title: Dexamethasone infusion in community-acquired pneumonia | |||||||||||||
Medical condition: pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2015-001109-15 | Sponsor Protocol Number: BIOTOB | Start Date*: 2015-12-15 | |||||||||||
Sponsor Name:INSTITUTO DE INVESTIGACION SANITARIA LA FE | |||||||||||||
Full Title: A Phase III clinical trial randomized and blinded on the use of inhaled tobramycin compared with placebo in patients undergoing mechanical ventilation and colonized by Gram negative bacteria for ef... | |||||||||||||
Medical condition: critically ill patients undergoing mechanical ventilation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001899-32 | Sponsor Protocol Number: RESINFENOL | Start Date*: 2017-08-17 |
Sponsor Name:Dr. Abelardo Aguilera Peralta | ||
Full Title: Crossover and randomized clinical trial on the effect of Resincolestiramine in the intestinal absorption of new uremic toxins in patients in hemodialysis with chronic renal insufficiency | ||
Medical condition: Chronic renal insufficiency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2022-003009-31 | Sponsor Protocol Number: HH007 | Start Date*: 2022-12-23 | |||||||||||
Sponsor Name:Zealand University Hospital, dept. of Haematology | |||||||||||||
Full Title: Atorvastatin for patients with Philadelphia-negative chronic myeloproliferative neoplasms - Essential thrombocythemia, polycythemia vera and prefibrotic myelofibrosis | |||||||||||||
Medical condition: Essential thrombocythemia, Polycythemia vera, prefibrotic myelofibrosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001919-31 | Sponsor Protocol Number: DALIAH | Start Date*: 2011-09-12 |
Sponsor Name:Roskilde sygehus | ||
Full Title: DALIAH A Danish Study of Low-dose Interferon Alpha Versus Hydroxyurea in the Treatment of Ph-negative Chronic Myeloid Neoplasias - A National Randomized Prospective Study With Focus on Efficacy,... | ||
Medical condition: Chronic myeloid neoplasms Essential thrombocythemia Polycythemia vera primary myelofibrosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000620-18 | Sponsor Protocol Number: RC20_0082 | Start Date*: 2021-02-19 | ||||||||||||||||
Sponsor Name:Nantes University Hospital | ||||||||||||||||||
Full Title: Human recombinant interferon gamma-1b for the prevention of hospital-acquired pneumonia in critically ill patients: a double-blind, international phase 2, randomized, placebo-controlled trial - the... | ||||||||||||||||||
Medical condition: Patients hospitalized in intensive care units, under mechanical ventilation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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