- Trials with a EudraCT protocol (759)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
759 result(s) found for: Respiratory Tract Diseases AND Thoracic Diseases.
Displaying page 4 of 38.
EudraCT Number: 2020-004951-34 | Sponsor Protocol Number: RESP301-005 | Start Date*: 2020-12-11 | ||||||||||||||||
Sponsor Name:Thirty Respiratory Limited | ||||||||||||||||||
Full Title: Community participants with COPD or bronchiectasis and at risk of Respiratory Viral Infections including SARS-CoV-2: An open-label, multicentre feasibility study of an inhaled nitric oxide generati... | ||||||||||||||||||
Medical condition: Chronic obstructive pulmonary disease (COPD) and bronchiectasis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003746-33 | Sponsor Protocol Number: REVC006 | Start Date*: 2020-09-30 | ||||||||||||||||||||||||||
Sponsor Name:ReViral Ltd. | ||||||||||||||||||||||||||||
Full Title: Randomized, double-blind, placebo-controlled trial of the safety, tolerability, and efficacy of RV521 in the treatment of adult subjects who have undergone hematopoietic cell transplantation (HCT) ... | ||||||||||||||||||||||||||||
Medical condition: Symptomatic RSV infection (upper airway involvement only) in subjects who have undergone HCT transplantation within 1 year of Randomization and who are moderately to severely immunocompromised. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Prematurely Ended) BE (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002533-32 | Sponsor Protocol Number: INS1007-201 | Start Date*: 2018-03-22 | ||||||||||||||||
Sponsor Name:Insmed Incorporated | ||||||||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multi-Center Study to Assess the Efficacy, Safety and Tolerability, and Pharmacokinetics of INS1007 Administered Once Daily for 24 We... | ||||||||||||||||||
Medical condition: Non-Cystic Fibrosis Bronchiectasis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) DK (Completed) SE (Completed) ES (Completed) NL (Completed) BG (Completed) PL (Completed) BE (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002193-27 | Sponsor Protocol Number: COVID-AT | Start Date*: 2020-06-15 | ||||||||||||||||
Sponsor Name:Cristina Avendano-Sola | ||||||||||||||||||
Full Title: Double-blind, randomized, controlled, clinical trial to assess the efficacy of allogenic mesenchymal stromal cells in patients with acute respiratory distress syndrome due to COVID-19 | ||||||||||||||||||
Medical condition: COVID-related Acute Respiratory Distress Syndrome | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001541-39 | Sponsor Protocol Number: BEVACOR | Start Date*: 2020-04-24 | ||||||||||||||||
Sponsor Name:Fundación para la Investigación Biomédica de Córdoba | ||||||||||||||||||
Full Title: Pilot study of single-dose bevacizumab as a treatment for acute respiratory distress syndrome in patients with COVID-19 | ||||||||||||||||||
Medical condition: Acute respiratory distress syndrome in patients with COVID-19 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022863-36 | Sponsor Protocol Number: FIBHGM-ECNC010-2010 | Start Date*: 2013-09-17 | |||||||||||
Sponsor Name:Fundación para la Investigación Biomédica del Hospital | |||||||||||||
Full Title: Phase IV, randomized and controlled study about efficacy an safety of the use of continuous pressure airway CPAP Bussignac in the immediate postoperative period of patients undergoing lung resect... | |||||||||||||
Medical condition: postoperative atelectasis / pneumonias | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002038-37 | Sponsor Protocol Number: 5.0 | Start Date*: 2012-03-06 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: Hyperpolarised xenon magnetic resonance imaging (Xe-129 MRI) lung imaging in COPD | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-005005-43 | Sponsor Protocol Number: FACEII | Start Date*: 2022-06-06 | |||||||||||
Sponsor Name:Consorci Mar Parc de Salut de Barcelona | |||||||||||||
Full Title: Ferinject in Addition to pulmonary rehabilitation in patients with COPD and iron deficiency to improve Exercise tolerance (FACE II study) | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001586-24 | Sponsor Protocol Number: | Start Date*: 2017-08-07 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: Delivering personalised care in the management of exacerbations of chronic obstructive pulmonary disease: A multi-centre randomised clinical trial | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003551-32 | Sponsor Protocol Number: ISS-U1111-1188-8695 | Start Date*: 2017-11-01 | |||||||||||
Sponsor Name:Hospital of South West Jutland | |||||||||||||
Full Title: Effects of GLP-1 receptor agonist treatment on pulmonary function and quality of life in obese patients with chronic obstructive pulmonary disease - A prospective, randomized, placebo-controlled, ... | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease in obese subjects | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004363-39 | Sponsor Protocol Number: MT-11 | Start Date*: 2018-03-15 | ||||||||||||||||
Sponsor Name:ALK-Abelló A/S | ||||||||||||||||||
Full Title: A phase III trial evaluating the efficacy and safety of the house dust mite (HDM) sublingual immunotherapy (SLIT)-tablet in children and adolescents (5-17 years) with HDM allergic asthma | ||||||||||||||||||
Medical condition: House Dust Mite (HDM) Allergic Asthma | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Temporarily Halted) HU (Completed) BG (Completed) DK (Completed) FR (Completed) PL (Completed) GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-003855-47 | Sponsor Protocol Number: AP301-II-002 | Start Date*: 2018-02-27 | ||||||||||||||||
Sponsor Name:Apeptico Forschung und Entwicklung GmbH | ||||||||||||||||||
Full Title: Safety and preliminary efficacy of sequential multiple ascending doses of solnatide to treat pulmonary permeability oedema in patients with moderate-to-severe ARDS - a randomised, placebo-controlle... | ||||||||||||||||||
Medical condition: pulmonary permeability oedema in patients with moderate-to-severe ARDS | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-005205-40 | Sponsor Protocol Number: RPL554-CO-203 | Start Date*: 2017-08-29 | |||||||||||
Sponsor Name:Verona Pharma plc | |||||||||||||
Full Title: A Phase IIb, randomized, double blind, placebo controlled, dose ranging study to assess the effect of RPL554 in patients with moderate to severe COPD. | |||||||||||||
Medical condition: moderate to severe Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) BG (Completed) GB (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002466-39 | Sponsor Protocol Number: MVD-PROT-001 | Start Date*: 2019-04-17 | |||||||||||
Sponsor Name:University Medical Center Groningen | |||||||||||||
Full Title: Morphine or Fentanyl for Refractory dyspnea in COPD | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease, COPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003331-32 | Sponsor Protocol Number: AZI003 | Start Date*: 2013-06-18 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:KULeuven and University Hospitals Leuven | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A PROSPECTIVE, RANDOMIZED, PLACEBO-CONTROLLED TRIAL OF PRE-TRANSPLANT AND PROMPT POST-TRANSPLANT TREATMENT WITH AZITHROMYCIN TO IMPROVE EARLY ALLOGRAFT FUNCTION AND OUTCOME AFTER LUNG TRANSPLANTA... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: EARLY LUNG ALLOGRAFT FUNCTION AND OUTCOME AFTER LUNG TRANSPLANTATION | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-002835-17 | Sponsor Protocol Number: 250774 | Start Date*: 2016-01-18 | ||||||||||||||||||||||||||
Sponsor Name:Justus Liebig Universität Gießen | ||||||||||||||||||||||||||||
Full Title: Investigation of the influence of PAH-specific medication on right ventricular function in patients with pulmonary arterial hypertension (PAH) under basal conditions | ||||||||||||||||||||||||||||
Medical condition: Pulmonary arterial Hypertension (PAH) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021782-70 | Sponsor Protocol Number: COALA-HE | Start Date*: 2011-06-22 | ||||||||||||||||
Sponsor Name:Universitätsmedizin der Johannes Gutenberg-Universität Mainz | ||||||||||||||||||
Full Title: Open monocentric clinical pilot study in COPD und Asthma patients to investigate static as well as dynamic ventilation, intrapulmonary ADC and pO2 using helium-3-MRI after inhalation of hyperpolar... | ||||||||||||||||||
Medical condition: The study is a diagnostic pilot study on COPD and Asthma patients | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000632-34 | Sponsor Protocol Number: AAUH-ICU-01 | Start Date*: 2017-04-25 | ||||||||||||||||
Sponsor Name:Department of Anaesthesia and Intensive Care Medicine, Aalborg University Hospital | ||||||||||||||||||
Full Title: Handling oxygenation targets in adults with acute hypoxaemic respiratory failure in the intensive care unit: A randomised clinical trial of a lower versus a higher oxygenation target Addendum: Tri... | ||||||||||||||||||
Medical condition: Acute hypoxaemic respiratory failure in patients admitted to the intensive care unit Addendum: Acute hypoxaemic respiratory failure in patients admitted to the intensive care unit with COVID-19 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005319-33 | Sponsor Protocol Number: BuS2020 | Start Date*: 2021-09-22 | |||||||||||
Sponsor Name:Fundación Cínic per a la Reserca Biomèdica | |||||||||||||
Full Title: EFFICACY AND SAFETY OF THE INTRATRACHEAL ADMINISTRATION OF BUDESONIDE WITH SURFACTANT IN VERY PRETERM INFANTS TO PREVENT BRONCHOPULMONARY DYSPLASIA: RANDOMIZED CLINICAL TRIAL | |||||||||||||
Medical condition: Bronchopulmonary dysplasia of prematurity | |||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012541-33 | Sponsor Protocol Number: D5127C00001 | Start Date*: 2009-08-11 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A randomised, placebo-controlled, double-blind (double-dummy technique), crossover, multi-centre study, to evaluate onset of effect in patients with Chronic Obstructive Pulmonary Disease (COPD) tre... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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