- Trials with a EudraCT protocol (1,312)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (57)
1,312 result(s) found for: Airway.
Displaying page 4 of 66.
EudraCT Number: 2008-000727-26 | Sponsor Protocol Number: HZC111348 | Start Date*: 2008-07-15 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: Study HZC111348, a repeat-dose study of GW685698/GW642444 Inhalation Powder versus placebo in the treatment of Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
Medical condition: Patients with Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005047-27 | Sponsor Protocol Number: CIB-ROF-2011-01 | Start Date*: 2012-01-24 | |||||||||||
Sponsor Name:CIBERES (Centro de Investigación Biomédica en Red Enfermedades Respiratorias) | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018763-42 | Sponsor Protocol Number: 2008CV17 | Start Date*: 2010-07-14 | ||||||||||||||||
Sponsor Name:University of Dundee | ||||||||||||||||||
Full Title: Do Phosphodiesterase 5 Inhibitors Improve Exercise Capacity in COPD Patients with Pulmonary Hypertension? | ||||||||||||||||||
Medical condition: Chronic obstructive pulmonary disease Pulmonary hypertension (secondary to 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: 2013-000262-11 | Sponsor Protocol Number: CCD_01535BC1_01 | Start Date*: 2013-09-24 | |||||||||||
Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
Full Title: An Open Label Placebo Study To Assess The Inhalation Profile Obtained By Acoustic Monitoring In COPD Patients Using The NEXThaler® Dry Powder Inhaler (DPI) Device. | |||||||||||||
Medical condition: COPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (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: 2010-022123-29 | Sponsor Protocol Number: ASA-COPD | Start Date*: 2010-11-25 | |||||||||||
Sponsor Name:Medical University of Vienna, Department of Clinical Pharmacology | |||||||||||||
Full Title: Acetylic salicylic acid for the treatment of Chronic Obstructive Pulmonary Disease (COPD). A randomized, double-blind, placebo-controlled trial | |||||||||||||
Medical condition: COPD II-III | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020818-28 | Sponsor Protocol Number: 10.0086 | Start Date*: 2010-10-14 | |||||||||||
Sponsor Name:St George's, University of London | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled trial of metformin in chronic obstructive pulmonary disease (COPD) exacerbations: a pilot study | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005210-44 | Sponsor Protocol Number: ASSET | Start Date*: 2009-07-07 | |||||||||||
Sponsor Name:Organisation name was not entered | |||||||||||||
Full Title: Teofilina a dosis bajas como potenciador del tratamiento anti-inflamatorio en EPOC grave (Estudio ASSET) | |||||||||||||
Medical condition: Enfermedad Pulmonar Obstructiva Crónica (EPOC) Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005148-16 | Sponsor Protocol Number: BO-EPOC-01 | Start Date*: 2006-07-06 | |||||||||||
Sponsor Name:MADAUS, S.A. | |||||||||||||
Full Title: Ensayo clínico randomizado, aleatorizado y doble ciego, para valorar el efecto del tratamiento con 320 mg al día de Acetato de Megestrol durante 8 semanas en los pacientes con Enfermedad Pulmonar O... | |||||||||||||
Medical condition: Pacientes afectos de enfermedad pulmonar obstructiva crónica (EPOC) severa definida según consenso ATS/ERS con un FEV1 <50% del valor teórico y con bajo peso corporal o pérdida de peso de forma in... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000340-13 | Sponsor Protocol Number: D9831C00001 | Start Date*: 2008-04-10 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A 4 week double-blind, placebo-controlled, randomized, parallel group phase IIa study to assess the efficacy and safety of AZD1981 in patients with moderate to severe Chronic Obstructive Pulmonary ... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) SK (Completed) DK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018987-17 | Sponsor Protocol Number: EP-101-02 | Start Date*: 2010-06-22 | |||||||||||
Sponsor Name:Elevation Pharmaceuticals, Inc. | |||||||||||||
Full Title: Randomized, Placebo-Controlled, Double-Blind, Dose Ranging, Single Dose, 6-Way Crossover Study to Assess the Safety, Efficacy and Pharmacokinetics of EP-101 Using eFlow Nebulizer in Patients with COPD | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000663-42 | Sponsor Protocol Number: CQAB149B2335SE | Start Date*: 2008-06-03 | |||||||||||
Sponsor Name:Novartis Farmacéutica S.A | |||||||||||||
Full Title: Extensión de 26 semanas del estudio multicéntrico, aleatorizado, doble ciego, controlado con placebo, con grupos paralelos y diseño adaptativo, de 26 semanas de tratamiento, para evaluar la segurid... | |||||||||||||
Medical condition: Enfermedad Pulmonar Obstructiva Crónica (EPOC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) DE (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-009096-35 | Sponsor Protocol Number: QGUY/2008/TA-270/-01 | Start Date*: 2009-03-12 | |||||||||||
Sponsor Name:Activus Pharma Co., Ltd | |||||||||||||
Full Title: An open-label, 28-day multiple dose pilot study to evaluate the effects on lung oxidative stress, safety and pharmacokinetics of TA-270 in patients with chronic obstructive pulmonary disease (COPD). | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease. ( COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017257-35 | Sponsor Protocol Number: R015 | Start Date*: 2010-02-25 | |||||||||||
Sponsor Name:Revotar Biopharmaceuticals AG | |||||||||||||
Full Title: Multi-center, randomized, double-blind, placebo-controlled, cross-over Phase II study to evaluate the safety and efficacy of inhaled Bimosiamose for the treatment of patients with moderate to sever... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
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: 2009-010084-16 | Sponsor Protocol Number: 6645 | Start Date*: 2009-07-24 | |||||||||||
Sponsor Name:Barts Health NHS Trust | |||||||||||||
Full Title: Randomised, Multi-Centre, Double-Blind, Placebo-Controlled Trial of Vitamin D Supplementation in Patients with Chronic Obstructive Pulmonary Disease | |||||||||||||
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: 2012-001585-14 | Sponsor Protocol Number: EPJ-2012 | Start Date*: 2013-01-10 | ||||||||||||||||
Sponsor Name:FISEVI | ||||||||||||||||||
Full Title: Effect of the elimination of colonization by Pneumocystis jirovecii on inflammatory response in patients with chronic obstructive pulmonary disease | ||||||||||||||||||
Medical condition: Chronic obstructive pulmonary disease | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003962-16 | Sponsor Protocol Number: D3540C00005 | Start Date*: 2007-11-27 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A 4-week double-blind, placebo-controlled, randomised, parallel group phase IIa study to assess the tolerability/safety and efficacy of inhaled AZD4818 in patients with moderate to severe Chronic O... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) SE (Completed) FI (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001168-28 | Sponsor Protocol Number: D5899C00001 | Start Date*: 2005-01-04 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A 12-month, double-blind, double-dummy, randomized, parallel group, multicenter efficacy and safety study of Symbicort® pMDI 2x160/4.5μg bid and 2x80/4.5 μg bid compared to Formoterol Turbuhaler 2x... | |||||||||||||
Medical condition: This is an application for a phase III study to be conducted in COPD patients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) HU (Completed) IS (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005534-20 | Sponsor Protocol Number: 05102006 | Start Date*: 2008-01-24 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: Effect of Erdosteine on inflammatory and oxidative biomarkers in sputum and exhaled breath in patients with COPD | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease (COPD) of different severity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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