- 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 7 of 66.
EudraCT Number: 2019-005005-43 | Sponsor Protocol Number: FACEII | Start Date*: 2022-06-06 | |||||||||||
Sponsor Name:Consorci Mar Parc de Salut de Barcelona | |||||||||||||
Full Title: Ferinject in Addition to pulmonary rehabilitation in patients with COPD and iron deficiency to improve Exercise tolerance (FACE II study) | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006173-33 | Sponsor Protocol Number: ALMED-07-C3-009 | Start Date*: 2009-10-09 | |||||||||||
Sponsor Name:Air Liquide | |||||||||||||
Full Title: An international phase III randomised trial comparing in severe Exacerbations of Chronic obstructive pulmonary disease the efficacy of Helium/Oxygen versus Air/Oxygen administered during spontaneo... | |||||||||||||
Medical condition: Patients eligible for this study are critically ill patients with COPD admitted in ICU for an exacerbation of their chronic disease with hypercapnic acute respiratory failure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) BE (Prematurely Ended) DE (Completed) IT (Ongoing) GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002237-73 | Sponsor Protocol Number: KOL-PH-SILD2008 | Start Date*: 2008-07-03 | ||||||||||||||||
Sponsor Name:Dept. of Pharmacology, Aarhus University | ||||||||||||||||||
Full Title: Sildenafil Treatment of COPD associated Pulmonary Hypertension | ||||||||||||||||||
Medical condition: Pulmonary hypertension in patients with chronic obstructive lung disease (COPD) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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: 2007-000666-20 | Sponsor Protocol Number: COPD1 | Start Date*: 2007-06-14 | |||||||||||
Sponsor Name:Royal Bournemouth Hospital | |||||||||||||
Full Title: Influence of insulin therapy in non-diabetic patients admitted to hospital with acute exacerbations of 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: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-004238-20 | Sponsor Protocol Number: CC21000 | Start Date*: 2024-02-06 | ||||||||||||||||
Sponsor Name:Vejle Hospital | ||||||||||||||||||
Full Title: BONG: Breathlessness and alternatives to Opioid treatment in Non-malign Groups of severe lung disease | ||||||||||||||||||
Medical condition: 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: 2017-003551-32 | Sponsor Protocol Number: ISS-U1111-1188-8695 | Start Date*: 2017-11-01 | |||||||||||
Sponsor Name:Hospital of South West Jutland | |||||||||||||
Full Title: Effects of GLP-1 receptor agonist treatment on pulmonary function and quality of life in obese patients with chronic obstructive pulmonary disease - A prospective, randomized, placebo-controlled, ... | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease in obese subjects | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003659-52 | Sponsor Protocol Number: PULSE | Start Date*: 2018-04-02 | |||||||||||
Sponsor Name:António Robalo Nunes | |||||||||||||
Full Title: Impact of Iron Deficiency treatment with intravenous ferric carboxymaltose in patients with Chronic Obstructive Pulmonary Disease: an open-label, randomized, 2-arm, no treatment control, parallel s... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease and Iron Deficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000919-24 | Sponsor Protocol Number: 0671 | Start Date*: 2018-08-13 | ||||||||||||||||
Sponsor Name:University of Leicester | ||||||||||||||||||
Full Title: A randomised placebo-controlled trial of anti-ST2 in COPD (COPD-ST2OP) | ||||||||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-023621-37 | Sponsor Protocol Number: CQVA149A2313 | Start Date*: 2011-02-23 | |||||||||||
Sponsor Name:Novartis Farmacéutica S. A | |||||||||||||
Full Title: Estudio multicéntrico, aleatorizado, doble ciego, con doble enmascaramiento, de grupos paralelos, de 26 semanas de tratamiento para evaluar la eficacia, seguridad y tolerabilidad de QVA149 en compa... | |||||||||||||
Medical condition: EPOC | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) HU (Completed) BE (Completed) LT (Completed) EE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006276-38 | Sponsor Protocol Number: A4471008 | Start Date*: 2007-06-27 | |||||||||||
Sponsor Name:Boehring Ingelheim Pharma Ges mbH, Regional Division Medicine, Regional Centre Vienna | |||||||||||||
Full Title: A 24 week, randomized, double-blind, placebo-controlled, multicenter study to evaluate the efficacy and safety of 18 MCG of Tiotropium inhalation capsules administered by Handihaler® once-daily plu... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) NL (Completed) GB (Completed) BE (Completed) GR (Completed) PT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000155-28 | Sponsor Protocol Number: PT009003 | Start Date*: 2016-11-21 | |||||||||||
Sponsor Name:Pearl Therapeutics, Inc. (Pearl) | |||||||||||||
Full Title: A Randomized, Double-Blind, Parallel Group, Multi-Center Study to Assess the Efficacy and Safety of PT009 compared to PT005 in Subjects With Moderate to Very Severe COPD | |||||||||||||
Medical condition: Moderate to Very Severe Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) BE (Completed) GB (Completed) DE (Completed) ES (Completed) AT (Completed) IT (Completed) | |||||||||||||
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: 2021-003797-30 | Sponsor Protocol Number: D9180C00003 | Start Date*: 2022-01-31 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase III, Multicentre, Randomized, Double-blind, Chronic-dosing, Parallel-group, Placebo-controlled Study to Evaluate the Efficacy and Safety of Two Dose Regimens of Tozorakimab in Participants ... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Trial now transitioned) FI (Trial now transitioned) DK (Trial now transitioned) SE (Trial now transitioned) NL (Trial now transitioned) ES (Ongoing) HU (Trial now transitioned) CZ (Trial now transitioned) BG (Trial now transitioned) PT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001120-18 | Sponsor Protocol Number: DYM | Start Date*: 2019-01-17 |
Sponsor Name:Stichting Pediatrisch Onderzoek Enschede | ||
Full Title: The protective effect of azelastine/fluticasone propionate (Dymista) on exercise-induced airway obstruction | ||
Medical condition: Exercise-induced airway obstruction Asthma Allergic rhinitis | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001160-29 | Sponsor Protocol Number: NAL-II-19-1 | Start Date*: 2019-06-24 | |||||||||||
Sponsor Name:LABORATOIRES SMB S.A | |||||||||||||
Full Title: A single blind, placebo controlled, three period, chronic dosing (6 weeks), multicentre, exploratory study to evaluate the effects of Nacystelyn (20 mg BID and 40 mg BID) on Functional Respiratory ... | |||||||||||||
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: 2012-002854-21 | Sponsor Protocol Number: CNVA237A2311 | Start Date*: 2013-02-19 | |||||||||||
Sponsor Name:Novartis Pharma Service AG | |||||||||||||
Full Title: A 26-week multi-center randomized double-blind study to compare efficacy and safety of NVA237 versus placebo as an add-on to maintenance therapy with fixed-dose combination salmeterol/fluticasone p... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) CZ (Prematurely Ended) SK (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
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 |
EudraCT Number: 2008-008394-63 | Sponsor Protocol Number: CNVA237A2303 | Start Date*: 2009-10-26 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 52-week treatment, randomized, double-blind, placebo-controlled, with open label tiotropium, parallel-group study to assess the efficacy, safety and tolerability of NVA237 in patients with chroni... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) HU (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002230-30 | Sponsor Protocol Number: D4260C00003 | Start Date*: 2008-07-28 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A 6 Week Double-Blind, Placebo-controlled, Randomised, Parallel Group Phase IIa Study to Assess the Tolerability/Safety and Efficacy of AZD1236 as an Oral Tablet in Patients with Moderate to Severe... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (study conducted in men or women, not of child bearing potential, aged 40 years or above). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) SK (Completed) HU (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
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