- Trials with a EudraCT protocol (181)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
181 result(s) found for: Pack-year.
Displaying page 1 of 10.
EudraCT Number: 2004-004247-22 | Sponsor Protocol Number: RES104033 | Start Date*: 2005-06-07 |
Sponsor Name:GlaxoSmithKline Research & Development Limited | ||
Full Title: A 28-day, Randomised, Double-Blind, Active Comparator, Controlled Study to Assess the Effects of Rosiglitazone, Inhaled Corticosteroid, Theophylline and Theophylline Plus Inhaled Corticosteroid on ... | ||
Medical condition: Smokers that are asthmatic | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-001093-26 | Sponsor Protocol Number: AZALEA | Start Date*: 2011-07-20 |
Sponsor Name:Imperial College, London | ||
Full Title: A Randomised, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy of Oral Azithromycin (500 Mg OD) as a Supplement to Standard Care for Adult Patients with Acute Exacerbations of Asthma | ||
Medical condition: Asthma (exacerbations of) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-009599-11 | Sponsor Protocol Number: 08/0339 | Start Date*: 2011-02-15 |
Sponsor Name:Joint UCLH/UCL/Royal Free Biomedical Research Unit | ||
Full Title: Prospective randomised cross over comparison on the physiological response to non-invasive ventilation using either Air O2 or Heliox21 | ||
Medical condition: Respiratory failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-002484-99 | Sponsor Protocol Number: 2006 | Start Date*: 2007-01-10 |
Sponsor Name:South Devon Health Care NHS Foundation Trust | ||
Full Title: The Use of Nebulised Magnesium Sulphate in Exacerbations of Chronic Obstructive Pulmonary Disease (COPD) | ||
Medical condition: We propose a study to examine whether adjuvant magnesium therapy administered via nebuliser is effective in the management of patients with acute exacerbations of COPD. The findings should help to ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000750-31 | Sponsor Protocol Number: 10376 | Start Date*: 2007-10-16 |
Sponsor Name:University Hospitals of Leciester NHS trust | ||
Full Title: The effect of long term low dose erythromycin on cough frequency in chronic unexplained cough: a randomised, double blind, placebo conrolled, parallel group trial | ||
Medical condition: Chronic unexplained cough | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003344-62 | Sponsor Protocol Number: mitHDAC | Start Date*: 2005-11-15 |
Sponsor Name:Imperial College | ||
Full Title: Effect of theophylline on histone deacetylase activity: enhancement of in-vitro glucocorticoid function in patients with COPD. | ||
Medical condition: Chronic Obstructive Lung Disease (COPD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-001524-38 | Sponsor Protocol Number: M/40464/30 | Start Date*: 2011-09-23 | |||||||||||
Sponsor Name:ALMIRALL, S. A. | |||||||||||||
Full Title: EFFICACY AND SAFETY OF ACLIDINIUM BROMIDE/FORMOTEROL FUMARATE FIXED-DOSE COMBINATIONS COMPARED WITH INDIVIDUAL COMPONENTS AND PLACEBO WHEN ADMINISTERED TO PATIENTS WITH STABLE CHRONIC OBSTRUCTIVE P... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) SK (Completed) HU (Completed) CZ (Completed) ES (Completed) FI (Completed) BE (Completed) DE (Completed) AT (Completed) DK (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002836-25 | Sponsor Protocol Number: QGUY/2004/IL 4-13/01 | Start Date*: 2004-12-15 |
Sponsor Name:Aerovance Inc. | ||
Full Title: A Phase IIa Study To Investigate The Effects of AER 001on Antigen Challenge In Atopic Asthmatic Subjects Following Repeated Administration. | ||
Medical condition: Asthma is characterised by an infiltration of the bronchial mucosa with activated T-lymphocytes (T-cells), eosinophils, and to a lessor extent polymorphonuclear leukocytes. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003561-13 | Sponsor Protocol Number: cro488 | Start Date*: 2006-12-04 |
Sponsor Name:imperial college | ||
Full Title: Reversal of steroid insensitivity in COPD by theophylline | ||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-001090-10 | Sponsor Protocol Number: D5892L00002 | Start Date*: 2005-08-17 |
Sponsor Name:AstraZeneca AB, AstraZeneca Sverige | ||
Full Title: A randomised, double blind, double dummy, multicentre phase III study comparing the efficacy of budesonide/formoterol (Symbicort® forte Turbuhaler®) and oral prednisolone + formoterol (Oxis® Turbuh... | ||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) FI (Completed) DK (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-015876-86 | Sponsor Protocol Number: SCB-004 | Start Date*: 2010-04-20 |
Sponsor Name:Southampton University Hospitals | ||
Full Title: An investigation into the mechanisms of action of a combined long acting beta agonist/inhaled corticosteroid (Seretide 500 accuhaler) on the bacterial colonisation, immunology and inflammation of p... | ||
Medical condition: Chronic Obstructive Pulmonary Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005857-23 | Sponsor Protocol Number: MC/PR/033011/003/05 | Start Date*: 2006-05-08 | |||||||||||
Sponsor Name:CHIESI | |||||||||||||
Full Title: DOUBLE BLIND, DOUBLE DUMMY, RANDOMISED, PARALLEL GROUP, MONOCENTRIC CLINICAL TRIAL ON THE EFFECTS OF CHF 1535 MDI OR SERETIDE DPI ON LUNG HYPERINFLATION AND EXERCISE TOLERANCE IN PATIENTS WITH COPD... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002952-17 | Sponsor Protocol Number: COPDIron | Start Date*: 2012-11-12 |
Sponsor Name:University of Oxford | ||
Full Title: Effects of intravenous iron on hypoxic pulmonary responses in COPD | ||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-003833-15 | Sponsor Protocol Number: MEU04/118A | Start Date*: 2006-11-21 |
Sponsor Name:South Manchester University NHS Trust [...] | ||
Full Title: A randomised parallel group study to investigate the effect of Seretide withdrawal in COPD using non-invasive biomarkers and physiological measurements | ||
Medical condition: Chronic Obstructive Pulmonary Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000338-10 | Sponsor Protocol Number: 0606 | Start Date*: 2006-02-24 |
Sponsor Name:NHS Lothian Health Board [...] | ||
Full Title: Can long term nebulised gentamicin reduce the bacterial burden, break the vicious cycle of inflammation and improve quality of life in patients with bronchiectasis? | ||
Medical condition: Bronchiectasis is respiratory disease with damaged airways. Such patients have frequent bacterial chest infections. The aim of our study is to assess whether nebulised gentamicin 80mg twice daily w... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-000789-11 | Sponsor Protocol Number: EL110006 | Start Date*: 2005-01-03 |
Sponsor Name:GlaxoSmithKline Research & Development Limited | ||
Full Title: A 12-week, randomised, double-blind, placebo-controlled, parallel-group multicentre study to evaluate the anti-inflammatory activity of GW842470 4mg twice daily on pulmonary hyperinflation in patie... | ||
Medical condition: Patients with moderate to severe stable chronic obstructive pulmonary disease (COPD) - Stage II or III | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) FI (Completed) ES (Completed) AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004401-79 | Sponsor Protocol Number: 00000000 | Start Date*: 2020-04-15 | ||||||||||||||||
Sponsor Name:University of Oxford, Clinical Trials and Research Governance | ||||||||||||||||||
Full Title: The use of Benralizumab, an interleukin-5 receptor-α monoclonal antibody as treatment of acute exacerbations of airways disease | ||||||||||||||||||
Medical condition: Asthma and COPD exacerbations. | ||||||||||||||||||
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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: 2008-001889-81 | Sponsor Protocol Number: IMD-10412003-1 | Start Date*: 2008-06-24 | |||||||||||
Sponsor Name:Institute of Medicinal Molecular Design, Inc. | |||||||||||||
Full Title: A Phase IIa, Proof of Concept Study to Evaluate the Reduction in Inflammatory Biomarkers and Assess Airway Function Following Administration of IMD-1041 in Patients with Chronic Obstructive Pulmona... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000311-15 | Sponsor Protocol Number: D9831C00002 | Start Date*: 2009-01-29 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Double-Blind, Placebo-Controlled, Randomised, Parallel Group Phase IIa Study to Evaluate the Histological Changes, Cellularity, Clinical Efficacy and Safety of AZD1981 in Patients with Moderate t... | ||
Medical condition: Chronic Obstructive Pulmonary Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-000046-21 | Sponsor Protocol Number: C0524T03 | Start Date*: 2004-11-22 |
Sponsor Name:Centocor BV | ||
Full Title: A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group, Dose-ranging Study Evaluating the Efficacy and Safety of CNTO 148 Administered Subcutaneously in Symptomatic Su... | ||
Medical condition: Severe persistent asthma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) CZ (Prematurely Ended) SE (Prematurely Ended) GB (Completed) IT (Prematurely Ended) | ||
Trial results: View results |
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