- 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 6 of 66.
EudraCT Number: 2006-004069-33 | Sponsor Protocol Number: CQAB149B2212 | Start Date*: 2006-10-24 | |||||||||||
Sponsor Name:NovartisPharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, double-dummy, active (formoterol 12 µg b.i.d) and placebo controlled, multi-center, 5 period crossover, dose-ranging study to assess the bronchodilatory efficacy and saf... | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005096-17 | Sponsor Protocol Number: 0633-009 | Start Date*: 2006-11-30 | |||||||||||
Sponsor Name:Merck & Co., Inc | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study, Conducted Under In-House blinding Conditions of MK-0633 in Patients With COPD | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006519-60 | Sponsor Protocol Number: D5892C00014 | Start Date*: 2007-05-22 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A multi-centre, randomised, double-blind, cross-over design study to evaluate efficacy on exercise tolerance of budesonide/formoterol (Symbicort®Turbuhaler®) 320/9 μg one inhalation twice daily com... | |||||||||||||
Medical condition: Severe Chronic 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: 2008-001396-30 | Sponsor Protocol Number: A7881010 | Start Date*: 2008-09-26 | |||||||||||
Sponsor Name:Pfizer Ltd, Ramsgate Road, Sandwich, Kent, UK | |||||||||||||
Full Title: A PHASE 2A, DOUBLE BLIND (3RD PARTY OPEN), 4 WAY CROSS-OVER, PLACEBO CONTROLLED STUDY TO INVESTIGATE THE PHARMACOKINETICS, SAFETY, TOLERATION AND EFFICACY OF SINGLE INHALED DOSES OF PF-00610355 IN ... | |||||||||||||
Medical condition: Chronic 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: 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: 2010-020141-26 | Sponsor Protocol Number: D3320C00001 | Start Date*: 2010-08-30 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Single-Centre, Randomised, Double-Blind, Placebo-Controlled, Parallel Group, Phase IIa Study to Investigate the Effects of 100mg AZD2423 as an oral tablet in Subjects with Mild COPD Following Seg... | |||||||||||||
Medical condition: Chronic 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: 2011-004152-19 | Sponsor Protocol Number: ELASTIC2011 | Start Date*: 2012-04-18 | |||||||||||
Sponsor Name:Ludwig Boltzmann institute for COPD and Respiratory Epidemiology | |||||||||||||
Full Title: Effects of ROFLUMILAST on markers of subclinical atherosclerosis In stable COPD; the ELASTIC-trial | |||||||||||||
Medical condition: chronic obstructive pulmonary disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (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: 2014-004899-35 | Sponsor Protocol Number: MORDYC | Start Date*: 2015-04-02 | |||||||||||
Sponsor Name:Maastricht University | |||||||||||||
Full Title: Morphine for palliative treatment of refractory dyspnea in patients with advanced COPD: benefits and respiratory adverse effects | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002089-39 | Sponsor Protocol Number: CFOR258F2402 | Start Date*: 2004-10-20 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, multi-center, placebo controlled 24 week study to compare the efficacy and safety of formoterol Certihaler™ 10µg b.i.d., tiotropium HandiHaler® 18µg o.d. and tiotropium HandiHaler® 1... | |||||||||||||
Medical condition: Stable chronic obstructive pulmonary disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) ES (Completed) CZ (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006976-31 | Sponsor Protocol Number: CQAB149B2341 | Start Date*: 2009-03-04 | |||||||||||
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: DK (Completed) ES (Completed) DE (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020917-97 | Sponsor Protocol Number: ARC209 | Start Date*: 2010-06-23 | ||||||||||||||||
Sponsor Name:ASSOCIAZIONE ITALIANA PNEUMOLOGI OSPEDALIERI | ||||||||||||||||||
Full Title: SPHERIC-1 (Sildenafil in the Chronic Obstructive Pulmonary Disease associated to Chronic Pulmonary Hypertension. Sixteen weeks long, multicentre, randomized, double blind study, in comparison with ... | ||||||||||||||||||
Medical condition: Moderate to severe pulmonary hypertension associated to moderate to mild COPD. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-003713-32 | Sponsor Protocol Number: A5641009 | Start Date*: 2005-11-29 | |||||||||||
Sponsor Name:Pfizer Ltd | |||||||||||||
Full Title: A phase II, randomized, double-blind, placebo-controlled, parallel group study to evaluate the efficacy and safety of UK-500,001 Dry Powder for Inhalation (DPI) in adults with moderate to severe Ch... | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease (COPD). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) ES (Completed) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001337-34 | Sponsor Protocol Number: D5892C00016 | Start Date*: 2007-08-24 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A double-blind, randomised, cross-over, multi-centre study, to evaluate onset of effect in the morning in patients with severe Chronic Obstructive Pulmonary Disease (COPD) treated with budesonide/f... | |||||||||||||
Medical condition: Severe Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DK (Completed) DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001801-26 | Sponsor Protocol Number: D5980C00023 | Start Date*: 2019-07-26 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Randomized, Open-Label, Two Period Crossover, Chronic Dosing, 1-Week, Pilot Study to Assess the Efficacy and Safety of Budesonide and Formoterol Fumarate Inhalation Aerosol Administered with a Sp... | |||||||||||||
Medical condition: Severe to Very Severe Chronic 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: 2011-002018-35 | Sponsor Protocol Number: ARC209/A | Start Date*: 2013-03-08 | ||||||||||||||||
Sponsor Name:ASSOCIAZIONE ITALIANA PNEUMOLOGI OSPEDALIERI | ||||||||||||||||||
Full Title: SPHERIC-1OE (Sildenafil and Pulmonary HypERtension In COPD – Open Extension) - A multicenter, longitudinal, 12 months open-label study, for the observation of the use of sildenafil in the treatment... | ||||||||||||||||||
Medical condition: Patients with pulmonary hypertension associated with chronic obstructive pulmonary disease enrolled in the study SPHERIC-1 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-006083-33 | Sponsor Protocol Number: AC2108378 | Start Date*: 2007-02-26 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, dose ascending, 2-cohort, parallel group study to examine the safety, tolerability, pharmacokinetics and pharmacodynamics of twice-daily inhaled dose... | |||||||||||||
Medical condition: Study is in COPD patients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003431-78 | Sponsor Protocol Number: C0168T70 | Start Date*: 2006-10-24 | |||||||||||
Sponsor Name:Centocor BV | |||||||||||||
Full Title: A Multicenter, Observational Study of the Long-term Safety of Infliximab (REMICADE®) in Subjects with Moderate to Severe Chronic Obstructive Pulmonary disease (COPD) | |||||||||||||
Medical condition: Moderate to severe COPD | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000288-89 | Sponsor Protocol Number: BY217/M2-121 | Start Date*: 2004-10-13 | |||||||||||
Sponsor Name:ALTANA Pharma AG | |||||||||||||
Full Title: A 24 week, double blind, randomized study to investigate the effect of 500 µg Roflumilast tablets once daily versus placebo on parameters indicative of hyperinflation in patients with chronic obstr... | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007775-17 | Sponsor Protocol Number: ALMED-07-C2-017 | Start Date*: 2009-10-14 | |||||||||||
Sponsor Name:Air Liquide | |||||||||||||
Full Title: A single centre, exploratory, phase II, cross-over, randomised trial, evaluating the effect of spontaneously breathing Helium/Oxygen (65%/35%), to either spontaneously breating Nitrogen/Oxygen (65%... | |||||||||||||
Medical condition: Severe chronic obstructive pneumonary disease (COPD) patients during a Six-Minute Walking Test | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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