- Trials with a EudraCT protocol (315)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5)
315 result(s) found for: Ventilator.
Displaying page 1 of 16.
EudraCT Number: 2008-000248-15 | Sponsor Protocol Number: Dartagnan3 | Start Date*: 2008-08-01 | |||||||||||
Sponsor Name:Association pour la promotion de la réanimation médicale à Tours | |||||||||||||
Full Title: Amikacine nébulisée à forte dose. Pharmacocinétique dans la pneumonie associée à la ventilation mécanique D’ARTAGNAN 3 | |||||||||||||
Medical condition: Ventilator associated pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006764-29 | Sponsor Protocol Number: KB001-04 | Start Date*: 2008-03-14 | |||||||||||
Sponsor Name:KaloBios Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, double-blind, placebo-controlled pilot study of KB001 in mechanically-ventilated patients colonized with pseudomonas aeruginosa | |||||||||||||
Medical condition: Patients with Pseudomonas aeruginosa Ventilator-Associated Pulmonary Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000442-12 | Sponsor Protocol Number: KB-101-002 | Start Date*: 2008-02-07 | |||||||||||
Sponsor Name:Kenta Biotech Ltd | |||||||||||||
Full Title: A non-comparative open pilot trial to assess the safety and pharmacokinetics of up to three single doses of AERUMAB 11 in patients with ventilator associated pneumonia caused by serotype O11 P. aer... | |||||||||||||
Medical condition: ventilator associated pneumonia (VAP) caused by serotype O11 Pseudomonas aeruginosa | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004470-28 | Sponsor Protocol Number: 2011RM010 | Start Date*: 2011-10-18 | |||||||||||
Sponsor Name:University Hospital of South Manchester | |||||||||||||
Full Title: Plasma and intrapulmonary population pharmacokinetics of piperacillin/tazobactam in critically ill patients | |||||||||||||
Medical condition: Critical illness, ventilator associated pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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: 2016-001054-17 | Sponsor Protocol Number: PHRN15-SE/AMIKINHAL | Start Date*: 2017-01-27 | |||||||||||
Sponsor Name:CHRU de Tours | |||||||||||||
Full Title: Double-blinded multicenter randomized controlled trial comparing inhaled amikacin versus placebo to prevent ventilator associated pneumonia | |||||||||||||
Medical condition: Patient with mechanical ventilation through an endotracheal tube | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004646-33 | Sponsor Protocol Number: DORINOS3008 | Start Date*: 2008-07-08 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Prospective, Randomized, Double-Blind, Double-Dummy, Multicenter Study to Assess the Safety and Efficacy of Doripenem Compared With Imipenem-Cilastatin in the Treatment of Subjects with Ventilato... | |||||||||||||
Medical condition: Ventilator-Associated Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) ES (Prematurely Ended) BE (Completed) PT (Prematurely Ended) DE (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001117-42 | Sponsor Protocol Number: DORI-NOS-2001 | Start Date*: 2007-10-18 | ||||||||||||||||
Sponsor Name:Janssen Cilag International NV | ||||||||||||||||||
Full Title: A Randomized, Open-Label, Multicenter Study to Assess the Safety and Tolerability of Doripenem Compared With Imipenem in the Treatment of Subjects With Complicated Intra-Abdominal Infections or Ven... | ||||||||||||||||||
Medical condition: ventilator-associated pneumonia complicated intra-abdominal infections | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-001472-14 | Sponsor Protocol Number: FibroCov-01 | Start Date*: 2020-05-06 |
Sponsor Name:Istituto Nazionale per le Malattie Infettive “Lazzaro Spallanzani” | ||
Full Title: AN OPEN-LABEL, RANDOMIZED, PARALLEL-ARM STUDY INVESTIGATING THE EFFICACY AND SAFETY OF INTRAVENOUS ADMINISTRATION OF PAMREVLUMAB VERSUS STANDARD OF CARE IN PATIENTS WITH SARS-COV-2 INFECTION | ||
Medical condition: Patients with documented SARS-CoV-2 infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-004006-96 | Sponsor Protocol Number: D4281C00001 | Start Date*: 2012-12-27 |
Sponsor Name:Astrazeneca AB | ||
Full Title: A Phase III, Randomized, Multicentre, Double-blind, Double-dummy, Parallel-group Comparative Study to Determine the Efficacy, Safety And Tolerability of Ceftazidime-Avibactam Versus Meropenem in th... | ||
Medical condition: nosocomial pneumonia (NP), ventilator-associated pneumonia (VAP) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) HU (Completed) GB (Completed) ES (Completed) IT (Prematurely Ended) PL (Completed) BG (Completed) LV (Completed) SI (Completed) LT (Prematurely Ended) GR (Completed) RO (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-005752-10 | Sponsor Protocol Number: AT-100/001 | Start Date*: 2023-04-20 | |||||||||||
Sponsor Name:Airway Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 1b, Randomized, Blinded, Dose-Determined Study Evaluating the Safety and Tolerability Profile of Intervention with AT-100 (rhSP-D) in Preterm Neonates at High Risk for the Development of Br... | |||||||||||||
Medical condition: Bronchopulmonary Dysplasia (BPD) | |||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019850-42 | Sponsor Protocol Number: ENB-010-10 | Start Date*: 2011-03-04 | |||||||||||
Sponsor Name:Alexion Pharma GmbH | |||||||||||||
Full Title: An Open-Label, Multicenter, Multinational Study of the Safety, Efficacy and Pharmacokinetics of Asfotase alfa (human recombinant tissue nonspecific alkaline phosphatase fusion protein) in Infants a... | |||||||||||||
Medical condition: Hypophosphatasia is a rare inborn error of bone metabolism caused by inactivating mutations in the gene encoding the Tissue-nonspecific alkaline phosphatase isoenzyme. With deficiency of Tissue-... | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) IT (Completed) ES (Completed) FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003020-23 | Sponsor Protocol Number: 1615R2132 | Start Date*: 2017-11-23 | |||||||||||||||||||||
Sponsor Name:Shionogi B.V. | |||||||||||||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Parallelgroup, Clinical Study of S-649266 Compared with Meropenem for the Treatment of Hospital-acquired Bacterial Pneumonia, Ventilator-associated Bacteria... | |||||||||||||||||||||||
Medical condition: Hospital-acquired Bacterial Pneumonia, Ventilator-associated Bacterial Pneumonia, or Healthcare-associated Bacterial Pneumonia Caused by Gram-negative Pathogens. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) GB (Completed) LV (Completed) HU (Completed) ES (Completed) BE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-001596-21 | Sponsor Protocol Number: POL7080-003 | Start Date*: 2013-08-19 |
Sponsor Name:Polyphor Ltd | ||
Full Title: A phase II, open-label, multi-center study to assess pharmacokinetics (PK), safety and efficacy of POL7080 co-administered with standard of care (SoC) treatment in patients with ventilator- associa... | ||
Medical condition: Ventilator- associated pneumonia due to suspected or documented Pseudomonas aeruginosa infection. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) GR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003933-27 | Sponsor Protocol Number: POL7080-011 | Start Date*: 2018-01-29 | |||||||||||
Sponsor Name:Polyphor Ltd. | |||||||||||||
Full Title: A multicenter, open-label, randomized, active-controlled, parallel group, pivotal study to investigate the efficacy, safety and tolerability, and pharmacokinetics of murepavadin combined with one a... | |||||||||||||
Medical condition: Ventilator-associated bacterial pneumonia (VABP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) EE (Prematurely Ended) ES (Prematurely Ended) FR (Prematurely Ended) HR (Completed) GR (Prematurely Ended) RO (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000735-41 | Sponsor Protocol Number: 2015_66 | Start Date*: 2016-09-06 | |||||||||||
Sponsor Name:CHRU LILLE | |||||||||||||
Full Title: Antimicrobial treatment in patients with ventilator-associated tracheobronchitis: a prospective randomized placebo-controlled double-blind multicenter trial | |||||||||||||
Medical condition: ventilator-associated pneumonitis | |||||||||||||
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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: 2012-003621-21 | Sponsor Protocol Number: CTBM100DDE04T | Start Date*: 2013-10-09 | |||||||||||
Sponsor Name:Charité University Hospital Berlin | |||||||||||||
Full Title: Prospective phase IIA multicenter double-blinded randomized placebo-controlled clinical trial evaluating the efficacy and safety of inhaled, aerosolized Tobramycin (TOBI®) b.i.d. in patients with v... | |||||||||||||
Medical condition: Intensive care unit patients with ventilation-associated pneumonia. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002121-30 | Sponsor Protocol Number: 1704R2133 | Start Date*: 2020-04-17 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Shionogi B.V. | ||||||||||||||||||||||||||||||||||||||
Full Title: An Open-label Study with a Nonrandomized Single-dose Phase in Subjects with Suspected or Confirmed Aerobic Gram-negative Bacterial Infections followed by a Randomized, Multiple-dose, Active-control... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Single dose: Pneumonia, cUTI, complicated intra-abdominal infections [cIAI], hospital acquired bacterial pneumonia [HABP]/ventilator-associated bacterial pneumonia [VABP], and sepsis or bloodstream... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: LT (Completed) GR (Completed) CZ (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000613-16 | Sponsor Protocol Number: CATCOVID-v1.2 | Start Date*: 2021-11-26 |
Sponsor Name:Charité – Universitätsmedizin Berlin | ||
Full Title: CCR1 antagonist treatment in patients hospitalized with COVID-19 A multi-centric, randomized, double-blind, and placebo-controlled clinical phase II trial | ||
Medical condition: Patients with acute SARS-CoV-2 infection, proven by a positive SARS-CoV-2 PCR test. The health status of the patients at inclusion in the clinical trial is rated 5 - 6 according to the WHO scale (s... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
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