- Trials with a EudraCT protocol (600)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
600 result(s) found for: Chronic Obstructive Pulmonary Disease (COPD).
Displaying page 6 of 30.
EudraCT Number: 2006-005819-10 | Sponsor Protocol Number: KKS-95 | Start Date*: 2007-12-07 | |||||||||||
Sponsor Name:Philipps-University Marburg | |||||||||||||
Full Title: Influence of tiotropium bromide (Spiriva ®) plus salbutamol versus salbutamol on the mucin secretion and sputum properties in subjects with a COPD exacerbation -TIBROMUC- | |||||||||||||
Medical condition: Anticholinergic bronchodilators, such as ipratropium bromide, may be used in combination with beta adrenergic agonists as SAlbutamol to produce bronchodilation in excess of that achieved by either ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004818-28 | Sponsor Protocol Number: CNVA237A2320 | Start Date*: 2015-07-13 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, parallel group, 26-week study evaluating the efficacy, safety and tolerability of NVA237 given once or twice daily, in patients with moderate and severe chronic obstruct... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) HU (Completed) BE (Completed) SE (Completed) GB (Completed) BG (Completed) PL (Completed) RO (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000179-38 | Sponsor Protocol Number: ESR-21-21168 | Start Date*: 2022-04-28 | |||||||||||
Sponsor Name:Bispebjerg Hospital | |||||||||||||
Full Title: Effects of blocking TSLP on airway inflammation and the epithelial immune-response to exacerbation triggers in patients with COPD A randomized double-blind, placebo-controlled trial of tezepelumab | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001933-84 | Sponsor Protocol Number: 1222.13 | Start Date*: 2008-11-18 | |||||||||||
Sponsor Name:Boehringer Ingelheim Finland Ky | |||||||||||||
Full Title: A Randomised, Double-Blind, Double-Dummy, Placebo-Controlled, Parallel Group Study to Assess the Efficacy and Safety of 48 Weeks of Once Daily Treatment of Orally Inhaled BI 1744 CL (5 μg [2 actuat... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) SE (Completed) DK (Completed) CZ (Completed) ES (Completed) IT (Completed) DE (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: 2017-004369-29 | Sponsor Protocol Number: 206854 | Start Date*: 2018-04-24 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: The Clinical Effectiveness of Fluticasone Furoate/Umeclidinium Bromide/Vilanterol in a Single Inhaler (TRELEGYTM ELLIPTATM) when Compared with Non-ELLIPTA Multiple Inhaler Triple Therapies in COPD ... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) which may be called emphysema or chronic bronchitis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) NL (Completed) ES (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: 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: 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: 2013-002966-38 | Sponsor Protocol Number: CCD-01535BC1-02 | Start Date*: 2013-11-20 | |||||||||||
Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
Full Title: A PHASE II, PARTIAL-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, 5-WAY CROSS-OVER CLINICAL PHARMACOLOGY STUDY TO EVALUATE THE PHARMACODYNAMICS OF BDP/B17MP AND FORMOTEROL ACROSS TWO DIFFERENT DOSE LEVELS... | |||||||||||||
Medical condition: COPD patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005909-19 | Sponsor Protocol Number: PAW002 | Start Date*: 2009-01-29 | |||||||||||
Sponsor Name:The University of Dundee | |||||||||||||
Full Title: Does extra fine HFA-BDP suppress small airways inflammation in COPD? | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004431-38 | Sponsor Protocol Number: P15099 | Start Date*: 2009-02-20 | |||||||||||
Sponsor Name:Imperial College | |||||||||||||
Full Title: ACE inhibition and mechanisms of skeletal muscle weakness in COPD | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease patients who have skeletal muscle weakness. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013686-26 | Sponsor Protocol Number: CQAB149BDE01 | Start Date*: 2009-10-16 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A randomized, double-blind, placebo controlled, multicenter, 3-period crossover study to compare the effect of indacaterol (150μg o.d.) on inspiratory capacity to placebo in patients with moderate ... | |||||||||||||
Medical condition: moderate chonic obstructive pulmonary disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: 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 |
EudraCT Number: 2009-016251-21 | Sponsor Protocol Number: 205.458 | Start Date*: 2010-10-29 | |||||||||||
Sponsor Name:Boehringer Ingelheim | |||||||||||||
Full Title: Pharmacokinetics and dose-ranging of tiotropium inhalation solution delivered from the Respimat inhaler 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: NL (Completed) DE (Completed) BE (Completed) FI (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004297-98 | Sponsor Protocol Number: 117113 | Start Date*: 2014-09-01 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: Study 117113: Mepolizumab vs. Placebo as add-on treatment for frequently exacerbating COPD patients characterized by eosinophil level. | |||||||||||||
Medical condition: Treatment of severe Chronic Obstructive Pulmonary Disease (COPD) in patients presenting frequent exacerbations | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) SK (Completed) DE (Completed) GB (Completed) DK (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000116-81 | Sponsor Protocol Number: SIL-COPD-01 | Start Date*: 2007-05-28 | ||||||||||||||||
Sponsor Name:Hospital Clinic Barcelona | ||||||||||||||||||
Full Title: Estudio de los efectos agudos de la administración de una dosis única de sildenafilo de 20 o 40 mg sobre el intercambio de gases y la hemodinámica pulmonar, en reposo y durante el esfuerzo, en paci... | ||||||||||||||||||
Medical condition: EPOC e hipertensión pulmonar asociada | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010668-40 | Sponsor Protocol Number: 1237.5 | Start Date*: 2011-07-29 | |||||||||||
Sponsor Name:Boehringer Ingelheim bv [...] | |||||||||||||
Full Title: A randomised, double-blind, parallel group study to assess the efficacy and safety of 52 weeks of once daily treatment of orally inhaled tiotropium + olodaterol fixed dose combination (2.5 μg / 5 μ... | |||||||||||||
Medical condition: Patients with Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) FI (Completed) PT (Completed) SI (Completed) CZ (Completed) DE (Completed) HU (Completed) DK (Completed) EE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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: 2008-008447-26 | Sponsor Protocol Number: CQAB149B2351 | Start Date*: 2009-03-02 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, controlled, parallel group, 12-week treatment study to compare the efficacy and safety of the combination of indacaterol 150 μg once daily with open label tiotropium 18 ... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) SK (Completed) HU (Completed) ES (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
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