- Trials with a EudraCT protocol (28)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
28 result(s) found for: Pneumonia severity index.
Displaying page 1 of 2.
EudraCT Number: 2020-001335-28 | Sponsor Protocol Number: IFX-1-P2.9 | Start Date*: 2020-03-29 | |||||||||||
Sponsor Name:InflaRx GmbH | |||||||||||||
Full Title: A pragmatic adaptive randomized controlled Phase II/III multicenter study of IFX-1 in Patients with severe COVID-19 Pneumonia - "PANAMO" | |||||||||||||
Medical condition: Severe pneumonia in context of COVID-19 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) BE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001406-15 | Sponsor Protocol Number: NACATB | Start Date*: 2018-07-19 | |||||||||||
Sponsor Name:Fundació Clínic per la Recerca Biomèdica | |||||||||||||
Full Title: Adequate duration of antibiotic treatment in community acquired pneumonia categorized by pneumonia severity index (PSI) | |||||||||||||
Medical condition: Community Acquired Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004894-25 | Sponsor Protocol Number: ATCC10AA_IS_ICDJ10-J18 | Start Date*: 2009-06-30 |
Sponsor Name:Karolinska University Hospital Huddinge | ||
Full Title: Effect of rosuvastatin on cardiovascular events and mortality after pneumonia | ||
Medical condition: Community aquired pneumonia | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001239-19 | Sponsor Protocol Number: PHRN14-PFD-CAPE_COD | Start Date*: 2015-08-14 | |||||||||||
Sponsor Name:CHRU de TOURS | |||||||||||||
Full Title: Effects of low-dose corticosteroids on survival of severe Community-Acquired Pneumonia | |||||||||||||
Medical condition: Severe community-acquired pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002994-39 | Sponsor Protocol Number: Cx611-0204 | Start Date*: 2016-04-06 |
Sponsor Name:TIGENIX, S.A.U. | ||
Full Title: A phase Ib/IIa, randomised, double blind, parallel group, placebo controlled, multicentre study to assess the safety and efficacy of expanded Cx611 allogeneic adipose-derived stem cells (eASCs) for... | ||
Medical condition: Severe community-acquired bacterial pneumonia requiring mechanical ventilation and/or vasopressors. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) BE (Completed) LT (Completed) GB (Completed) FR (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001710-32 | Sponsor Protocol Number: 2006-101 | Start Date*: 2006-07-05 |
Sponsor Name:Dept. of Anaesthesia, Centre of Head and Orthopaedics, Copenhagen University Hospital Rigshospitalet | ||
Full Title: PeRioperative OXygen fraction – effect on surgical site Infection and pulmonary complications after abdominal surgery. (The PROXI-study) | ||
Medical condition: Laparotomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-006951-32 | Sponsor Protocol Number: REP0321 | Start Date*: 2022-04-05 | |||||||||||
Sponsor Name:Dompé farmaceutici s.p.a. | |||||||||||||
Full Title: Reparixin 1200 mg three times a day as add-on therapy to standard of care to limit disease progression in hospitalised adult patients with COVID-19 and other community-acquired pneumonia. A multina... | |||||||||||||
Medical condition: COVID-19 and other community-acquired pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001870-32 | Sponsor Protocol Number: CDFV890D12201 | Start Date*: 2020-07-10 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: Phase 2, randomized, controlled, open label multi-center study to assess efficacy and safety of DFV890 for the treatment of SARS-CoV-2 infected patients with COVID-19 pneumonia and impaired respira... | |||||||||||||
Medical condition: COVID-19 pneumonia and impaired respiratory function | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) DK (Completed) NL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001255-40 | Sponsor Protocol Number: STRIKE-SARS-CoV2 | Start Date*: 2020-04-16 | |||||||||||
Sponsor Name:Clínica Universidad de Navarra/Universidad de Navarra | |||||||||||||
Full Title: Sarilumab Treatment In cytoKinE storm caused by infection with COVID-19. | |||||||||||||
Medical condition: Severe pneumonia caused by infection with SARS CoV 2. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001303-16 | Sponsor Protocol Number: 7747 | Start Date*: 2020-04-11 |
Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||
Full Title: Efficacy of Hydroxychloroquine, Telmisartan and Azithromycin on Survival in Elderly Hospitalized Patients with VIDOC-19 : A Randomized, Multi-Centre, Adaptive, Blinded Study | ||
Medical condition: COVID-19 infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002056-20 | Sponsor Protocol Number: APHP200495 | Start Date*: 2020-10-14 |
Sponsor Name:Assistance Publique -Hôpitaux de Paris | ||
Full Title: FX06 to rescue acute respiratory distress syndrome during Covid-19 pneumonia : FX-COVID | ||
Medical condition: Patients admitted in participating ICUs who received mechanical ventilation for SARS-CoV-2 induced acute respiratory distress syndrome (ARDS) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-005097-25 | Sponsor Protocol Number: KIDS-STEP | Start Date*: Information not available in EudraCT |
Sponsor Name:Universitätskinderspital beider Basel (UKBB) | ||
Full Title: A randomised placebo-controlled multi-centre effectiveness trial of adjunct betamethasone therapy in hospitalised children with community acquired pneumonia (CAP) | ||
Medical condition: Children with community acquired pneumonia (CAP). | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001760-29 | Sponsor Protocol Number: ALCOVID-19 | Start Date*: 2020-09-09 |
Sponsor Name:Sociedad Española de Farmacia Hospitalaria | ||
Full Title: Phase II clinical trial to evaluate the efficacy and safety of inhaled ethanol in the treatment of early-stage COVID-19. | ||
Medical condition: COVID-19 | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003775-39 | Sponsor Protocol Number: F1D-MC_X311 | Start Date*: 2008-10-29 |
Sponsor Name:Charité – Universitätsmedizin Berlin | ||
Full Title: Randomised, placebo-controlled parallel-group trial to evaluate an oral dose of 10 mg Olanzapin combined with Riluzol for the treatment of appetite loss on patients with amyotrophic lateral sklerosis | ||
Medical condition: patients with amyotrophic lateral sclerosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-005676-25 | Sponsor Protocol Number: AC16025 | Start Date*: 2016-08-31 | ||||||||||||||||
Sponsor Name:University of Edinburgh [...] | ||||||||||||||||||
Full Title: Sensing using Neutrophil Activation Probe on the Intensive Therapy Unit | ||||||||||||||||||
Medical condition: Critical illness requiring ventilation | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003268-25 | Sponsor Protocol Number: AT-03A-017 | Start Date*: 2023-05-12 | |||||||||||
Sponsor Name:Atea Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Bemnifosbuvir in High-Risk Outpatients with COVID-19 | |||||||||||||
Medical condition: COVID-19 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) ES (Ongoing) LV (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003240-25 | Sponsor Protocol Number: FIBHGM-ECNC003-2021 | Start Date*: 2023-06-01 |
Sponsor Name:Fundación para la Investigación Biomédica del Hospital Gregorio Marañón | ||
Full Title: PHASE I/IIa OPEN CLINICAL TRIAL TO EVALUATE THE SAFETY AND EFFICACY OF ALLOGENIC ADMINISTRATION OF TREG CELLS OBTAINED FROM THYMAL TISSUE (thyTreg) IN THE CONTROL OF IMMUNOLOGICAL HYPERACTIVATION ... | ||
Medical condition: immune hyperactivation in COVID-19 patients | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004166-23 | Sponsor Protocol Number: A1481157 | Start Date*: 2015-05-11 |
Sponsor Name:Pfizer, Inc. | ||
Full Title: A 7-Day, Open-Label, Multicenter, Pharmacokinetic (PK) Study (Part 1) Followed by A 7-Day, Randomized, Multicenter, Double-Blind, Placebo-Controlled, Dose-Ranging, Parallel Group Study (Part 2) of ... | ||
Medical condition: Persistent Pulmonary Hypertension of the Newborn (PPHN) or Hypoxic Respiratory Failure and at Risk for PPHN | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2020-003125-39 | Sponsor Protocol Number: TRI-08892 | Start Date*: 2020-10-12 |
Sponsor Name:Thrombosis Research Institute | ||
Full Title: Early thromboprophylaxis in COVID-19 (ETHIC trial): an open label, randomized phase IIIb trial of community-based prophylactic low-molecular-weight heparin (LMWH) versus standard of care (no enoxap... | ||
Medical condition: Confirmed diagnosis of SARS-CoV-2 with symptomatic COVID-19 infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-023777-19 | Sponsor Protocol Number: SToP-BPD | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: Systemic Hydrocortisone To Prevent Bronchopulmonary Dysplasia in preterm infants: the SToP-BPD study | |||||||||||||
Medical condition: bronchopulmonary dysplasia | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) BE (Completed) | |||||||||||||
Trial results: (No results available) |
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