- Trials with a EudraCT protocol (223)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
223 result(s) found for: COPD exacerbation.
Displaying page 1 of 12.
EudraCT Number: 2019-004178-24 | Sponsor Protocol Number: 1704 | Start Date*: 2020-06-13 | ||||||||||||||||
Sponsor Name:Amphia | ||||||||||||||||||
Full Title: Defining long-term macrolide maintenance therapy in COPD: a single center randomized controlled trial: | ||||||||||||||||||
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: 2019-001800-39 | Sponsor Protocol Number: D3251C00014 | Start Date*: 2019-11-14 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Chronic-dosing, Parallel-group, Placebo-controlled Phase 3 Study to Evaluate the Efficacy and Safety of Benralizumab 100 mg in Patients with Moderate to V... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) PL (Trial now transitioned) HU (Trial now transitioned) CZ (Trial now transitioned) DE (Trial now transitioned) AT (Trial now transitioned) ES (Ongoing) GB (GB - no longer in EU/EEA) NL (Ongoing) BE (Trial now transitioned) GR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004872-76 | Sponsor Protocol Number: RECUT-Trial | Start Date*: 2020-05-07 | |||||||||||
Sponsor Name:Medizinische Universtitätsklinik, Kantonsspital Baselland | |||||||||||||
Full Title: Reduction of corticosteroid use in outpatient treatment of exacerbated COPD – a randomized, double-blind, non-inferiority study (The “RECUT”-Trial) | |||||||||||||
Medical condition: acute exacerbation of COPD; acute exacerbation (defined solely by clinical parameters according to the Anthonisen criteria, meaning ≥2 of the following: change of baseline dyspnea, change of cough,... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003253-28 | Sponsor Protocol Number: MV130-SLG-001 | Start Date*: 2012-12-13 | |||||||||||
Sponsor Name:Inmunotek S.L. | |||||||||||||
Full Title: Randomized double-blind placebo-controlled prospective, parallel, multicentre clinical trial of bacterial polivalent vaccine (BACTEK ®)administered by sublingual mucosa in subjects with chronic o... | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003441-26 | Sponsor Protocol Number: Protocol_CORTICO-COP_PSJUJ | Start Date*: 2016-03-02 | |||||||||||
Sponsor Name:Chronic Obstructive Pulmonary Disease Trial Network (COP:TRIN) | |||||||||||||
Full Title: CORTICO-COP (CORTICOsteroid reduction in COPD) trial | |||||||||||||
Medical condition: 1) Whether a reduction of the dose systemic corticosteroids (SC) therapy in patients with acute exacerbation of COPD(AE-COPD) - compared with AE-COPD patients in the standard treatment- leading to ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003075-35 | Sponsor Protocol Number: CTT116855 | Start Date*: 2014-07-24 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A phase III, 52 week, randomized, double-blind, 3-arm parallel group study, comparing the efficacy, safety and tolerability of the fixed dose triple combination fluticasone furoate/ umeclidinium/vi... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) FI (Completed) PL (Completed) SE (Completed) DE (Completed) AT (Completed) CZ (Completed) BE (Completed) DK (Completed) ES (Completed) NO (Completed) RO (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019685-87 | Sponsor Protocol Number: RO-2455-404-RD | Start Date*: 2011-04-27 | |||||||||||
Sponsor Name:Takeda Pharma A/S | |||||||||||||
Full Title: Effect of roflumilast on exacerbation rate in patients with COPD treated with fixed combinations of LABA and ICS. A 52-week, randomised double-blind trial with roflumilast 500 μg versus placebo | |||||||||||||
Medical condition: severe chronic obstructive pulmonary disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) DE (Completed) AT (Completed) DK (Completed) GR (Completed) NL (Completed) HU (Completed) SK (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003937-42 | Sponsor Protocol Number: BY217/M2-124 | Start Date*: 2005-06-16 | |||||||||||
Sponsor Name:ALTANA Pharma AG | |||||||||||||
Full Title: Effect of roflumilast on exacerbation rate in patients with COPD A 52 weeks, double-blind study with 500 mcg roflumilast once daily versus placebo | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) HU (Completed) GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004166-16 | Sponsor Protocol Number: SimvaCOPD | Start Date*: 2012-08-07 | ||||||||||||||||
Sponsor Name:Abteilung für Pulmologie, Landesklinikum Thermenregion Hochegg | ||||||||||||||||||
Full Title: Does simvastatin treatment affect COPD exacerbations? - Evaluation in a randomized controlled trial | ||||||||||||||||||
Medical condition: patients with COPD in stage II-IV (according to the GOLD classification) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002275-28 | Sponsor Protocol Number: 1237.19 | Start Date*: 2014-11-18 | |||||||||||
Sponsor Name:Boehringer Ingelheim Finland Ky | |||||||||||||
Full Title: A randomised, double-blind, active-controlled parallel group study to evaluate the effect of 52 weeks of once daily treatment of orally inhaled tiotropium + olodaterol fixed dose combination compar... | |||||||||||||
Medical condition: chronic obstructive pulmonary disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) IT (Completed) SE (Completed) PT (Completed) DK (Completed) BE (Completed) NL (Completed) HU (Completed) GB (Completed) ES (Completed) AT (Completed) IE (Completed) LT (Completed) CZ (Completed) LV (Completed) SK (Completed) DE (Completed) SI (Completed) GR (Completed) BG (Completed) HR (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004048-21 | Sponsor Protocol Number: 7171L01 | Start Date*: 2006-12-29 | |||||||||||
Sponsor Name:ZAMBON GROUP | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED, PARALLEL GROUPS STUDY ON EFFICACY AND SAFETY OF NAC 600 MG DAILY AND NAC 1200 MG DAILY AS MUCOLYTIC AGENT IN THE TREATMENT OF CHRONIC OBSTRUCTIVE PUL... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Bronchitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004966-16 | Sponsor Protocol Number: CQVA149A2318 | Start Date*: 2013-02-27 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A 52-week treatment, multi-center, randomized, double-blind, double-dummy, parallel-group, active controlled study to compare the effect of QVA149 (indacaterol maleate / glycopyrronium bromide) wit... | |||||||||||||
Medical condition: subjects with moderate to very severe COPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) HU (Completed) SE (Completed) ES (Completed) AT (Completed) LT (Completed) NL (Completed) CZ (Completed) FI (Completed) DE (Completed) BE (Completed) IS (Completed) IT (Completed) PT (Completed) NO (Completed) PL (Completed) EE (Completed) DK (Completed) BG (Completed) LV (Completed) GR (Completed) GB (Completed) LU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004755-11 | Sponsor Protocol Number: IWT- vlaanderen | Start Date*: 2007-11-29 | ||||||||||||||||
Sponsor Name:University Hospital, Catholic University of Leuven | ||||||||||||||||||
Full Title: Vitamin D as treatment for COPD | ||||||||||||||||||
Medical condition: This project aims to explore the relationship between Vitamin D deficiency and COPD progression via a prospective randomised placebo-controlled study. For this purpose, 180 patients hospitalised wi... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-013256-69 | Sponsor Protocol Number: CQVA149A2304 | Start Date*: 2010-04-13 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: A 64-week treatment, multi-center, randomized, double-blind, parallel-group, active controlled study to evaluate the effect of QVA149 (110/50 μg o.d.) vs NVA237 (50 μg o.d.) and open-label tiotropi... | ||||||||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) HU (Completed) FI (Completed) CZ (Completed) NL (Completed) SK (Completed) ES (Completed) GB (Completed) DK (Completed) FR (Completed) EE (Completed) IE (Completed) IT (Completed) PL (Completed) AT (Completed) GR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-002724-33 | Sponsor Protocol Number: RECHMPL19-0069 | Start Date*: 2019-11-15 |
Sponsor Name:University Hospital of Montpellier | ||
Full Title: Eosinophil-driven corticotherapy for patients hospitalized for COPD exacerbation: a double-blind, randomized, controlled trial | ||
Medical condition: The study population corresponds to patients hospitalized for COPD exacerbation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005660-13 | Sponsor Protocol Number: He-08-01 | Start Date*: 2008-12-11 | |||||||||||
Sponsor Name:BOC Ltd. | |||||||||||||
Full Title: COPD exacerbation - Heliox Therapy - Assessment Heliox vs. Medical Air in Acute Exacerbation of Chronic Obstructive Pulmonary Disease: A Pilot Randomised Controlled Trial | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002498-80 | Sponsor Protocol Number: 06062019 | Start Date*: 2019-09-24 | |||||||||||
Sponsor Name:Mikkel Brabrand | |||||||||||||
Full Title: Will titrated oxygen flow to a peripheral oxygen saturation of 88-92% compared with oxygen flow to a saturation >94% reduce mortality in Chronic Obstructive Pulmonary Disease patients with acute ex... | |||||||||||||
Medical condition: Acute COPD Exacerbation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000832-42 | Sponsor Protocol Number: n/a | Start Date*: 2008-11-05 | |||||||||||
Sponsor Name:East Kent Hospital Trust | |||||||||||||
Full Title: Effectiveness of Heliox in Hypercapnic Respiratory Failure | |||||||||||||
Medical condition: Hypercapnic Respiratory Failure due to excerbation of Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002826-58 | Sponsor Protocol Number: 1 | Start Date*: 2020-02-05 | |||||||||||
Sponsor Name:Rijnstate Hospital, Arnhem | |||||||||||||
Full Title: The effects of enoximone in acute exacerbation COPD: a pilot study | |||||||||||||
Medical condition: Acute exacerbation of COPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002905-31 | Sponsor Protocol Number: RO-2455-405-RD | Start Date*: 2011-12-01 | ||||||||||||||||
Sponsor Name:Nycomed GmbH | ||||||||||||||||||
Full Title: Effect of roflumilast 500 μg tablets once daily at acute COPD exacerbations treated with standard therapy of oral steroids and antibiotics. A randomised, double-blind, placebo-controlled, parallel-... | ||||||||||||||||||
Medical condition: Acute exacerbations of chronic obstructive pulmonary disease (COPD) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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