- Trials with a EudraCT protocol (766)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
766 result(s) found for: Exacerbation.
Displaying page 1 of 39.
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: 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: 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: 2017-001074-42 | Sponsor Protocol Number: 200879 | Start Date*: 2017-12-01 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd. | |||||||||||||
Full Title: A Phase IIb, Randomized (Stratified), Double-Blind (Sponsor Open), Parallel-Group, Placebo-Controlled, Dose-Finding Study of Nemiralisib (GSK2269557) Added to Standard of Care (SoC) Versus SoC Alon... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) SE (Prematurely Ended) GB (Prematurely Ended) PL (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) RO (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007275-16 | Sponsor Protocol Number: InfQ-001 | Start Date*: 2008-12-18 | |||||||||||
Sponsor Name:Department of Infetious Diseases, Odense University Hospital | |||||||||||||
Full Title: Antibiotic treatment in patients hospitalized with an acute exacerbation in chronic obstructive pulmonary disease. Effect of one day of antibiotic treatment compared t0 6 days of antibiotic treatme... | |||||||||||||
Medical condition: Acute exacerbation of chronic ostructive pulmonary disease in hospitalized patients. All patients receive "standard of care", and 1 day of intravenous antibiotics. In addition patients are randomiz... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004986-99 | Sponsor Protocol Number: NBTCS02 | Start Date*: 2017-01-11 | |||||||||||
Sponsor Name:NovaBiotics, Ltd | |||||||||||||
Full Title: A Randomized, Double-Blind, Parallel Group, Placebo-Controlled Study Investigating the Optimal Dose Regimen, Efficacy, and Safety of Adding Oral Cysteamine in Adult Patients with Cystic Fibrosis (C... | |||||||||||||
Medical condition: exacerbation of Cystic Fibrosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) GB (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: 2006-003944-42 | Sponsor Protocol Number: REP-FAR-005 | Start Date*: 2006-12-22 | |||||||||||
Sponsor Name:REPLIDYNE, INC. | |||||||||||||
Full Title: Prospective, Randomized, Double-Blind Trial to Evaluate the Efficacy and Safety of Faropenem Medoxomil 600 mg PO, BID for 5 Days Versus Placebo Versus Telithromycin In the Treatment of Acute Exacer... | |||||||||||||
Medical condition: Acute Exacerbation of Chronic Bronchitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) LV (Completed) BG (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: 2007-000006-67 | Sponsor Protocol Number: PIRRI/CT/001 | Start Date*: 2007-10-29 | |||||||||||
Sponsor Name:LALLEMAND PHARMA INTERNATIONAL | |||||||||||||
Full Title: Sub-lingual administration of a Polyvalent Mechanical Bacterial Lysate (PMBL) in patients with Moderate or Severe and very Severe Chronic Obstructive Pulmonary Disease (COPD) according to GOLD clas... | |||||||||||||
Medical condition: Patients with documented moderate, severe and very severe COPD. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004558-13 | Sponsor Protocol Number: Z7224L02 | Start Date*: 2017-05-30 | |||||||||||
Sponsor Name:Zambon S.p.A. | |||||||||||||
Full Title: A double-blind, placebo controlled, multicentre, clinical trial to investigate the efficacy and safety of 12 months of therapy with inhaled Promixin® (colistimethate sodium) in the treatment of sub... | |||||||||||||
Medical condition: Non-cystic fibrosis bronchiectasis chronically infected with Pseudomonas aeruginosa | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) PL (Completed) DE (Completed) PT (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004807-67 | Sponsor Protocol Number: APOTEL01 | Start Date*: 2009-01-15 | |||||||||||
Sponsor Name:University of Athens, Medical School | |||||||||||||
Full Title: AN OPEN-LABEL, NON-RANDOMIZED PHASE IV CLINICAL TRIAL OF THE EFFICACY OF INTRAVENOUSLY ADMINISTERED 1000MG PARACETAMOL AS ANTIPYRETIC AND ANALGESIC MEDICATION | |||||||||||||
Medical condition: Fever and pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
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: 2006-003886-15 | Sponsor Protocol Number: TELIT L 01747 | Start Date*: 2006-09-12 | |||||||||||
Sponsor Name:SANOFI-AVENTIS S.P.A | |||||||||||||
Full Title: Steady state telithromycin pharmacokinetics and pharmacodynamic in adult patients with mild-moderate acute exacerbation of chronic obstructive pulmonary disease treated with a standard oral dos... | |||||||||||||
Medical condition: Acute exacerbation of chronic-obstructive pulmonary disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
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: 2009-017051-10 | Sponsor Protocol Number: 09-313 | Start Date*: 2010-07-13 | |||||||||||
Sponsor Name:UMC Utrecht | |||||||||||||
Full Title: Metabolic adverse events before and after glucocorticoid pulse therapy in rheumatoid arthritis | |||||||||||||
Medical condition: Patients with rheumatoid arthritis, who suffer from a exacerbation of disease can be included in this study. Exacerbation is defined as a Disease Activity Score of 5.1 or higher. Patients will be e... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006096-37 | Sponsor Protocol Number: BAY 12-8039/11980 | Start Date*: 2008-05-09 | |||||||||||
Sponsor Name:Bayer HealthCare AG, Leverkusen, Germany | |||||||||||||
Full Title: A prospective, multinational, multicenter, randomized, double-blind, double-dummy, controlled study comparing the efficacy and safety of moxifloxacin to that of amoxicillin-clavulanic acid for the ... | |||||||||||||
Medical condition: acute exacerbation of chronic bronchitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Completed) IE (Completed) BE (Completed) DE (Completed) ES (Completed) PT (Completed) GR (Completed) LT (Completed) LV (Completed) IT (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004351-39 | Sponsor Protocol Number: FARM8MXYFL | Start Date*: 2011-10-28 | |||||||||||||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||||||||||||
Full Title: Phase II, randomized, double arm, multi-center study evaluating the efficacy and safety of azithromycin for the long term prophylactic treatment of COPD in primary antibody deficiency patients with... | |||||||||||||||||||||||
Medical condition: primary immunodefciency patients with COPD and frequent exacerbations | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
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: 2008-003842-27 | Sponsor Protocol Number: Studio-flourochinoloni-in-BPCO. | Start Date*: 2008-10-14 |
Sponsor Name:CENTRO STUDI FADOI | ||
Full Title: Randomized, single-blind, parallel groups, controlled study to compare levofloxacin and prulifloxacin in patients with exacerbations of COPD previously treated with different antibiotics and admitt... | ||
Medical condition: - Patients with acute exacerbation of COPD of possible infectious origin, previously treated with antibiotic therapy (no quinolones), without clinical improvement, and hospitalized in Internal Medi... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
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