- Trials with a EudraCT protocol (57)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
57 result(s) found for: Bronchitis AND Chronic Bronchitis AND Cough.
Displaying page 1 of 3.
EudraCT Number: 2004-000404-40 | Sponsor Protocol Number: BAY 12-8039/11229 | Start Date*: 2004-09-06 | |||||||||||
Sponsor Name:Bayer plc | |||||||||||||
Full Title: A double-blind, randomised, placebo controlled study to investigate chronic intermittent “pulse” therapy of moxifloxacin as a prevention of acute exacerbation in out-patients with chronic bronchitis. | |||||||||||||
Medical condition: Chronic bronchitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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: 2018-002563-25 | Sponsor Protocol Number: IJG-AB4T-2018 | Start Date*: 2018-11-15 | |||||||||||
Sponsor Name:IDIAP Jordi Gol | |||||||||||||
Full Title: Effectiveness of antitussive, anticholinergic and honey therapy versus usual practice in adults with uncomplicated acute bronchitis [AB4T study] | |||||||||||||
Medical condition: Cough in the context of acute bronchitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000851-15 | Sponsor Protocol Number: UoB1581 | Start Date*: 2012-10-25 | |||||||||||
Sponsor Name:University of Bristol | |||||||||||||
Full Title: What is the clinical and cost effectiveness of oral steroids in the treatment of acute lower respiratory tract infection (LRTI)? A placebo controlled randomised trial | |||||||||||||
Medical condition: Acute lower respiratory tract infection/bronchitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004143-11 | Sponsor Protocol Number: 33103 | Start Date*: 2008-12-17 | |||||||||||
Sponsor Name:The University of Nottingham | |||||||||||||
Full Title: Are macrolide antibiotics effective in chronic idiopathic cough? | |||||||||||||
Medical condition: idiopathic chronic cough, defined as cough with no identifiable cause and which has been present for at least 2 monhs. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000712-29 | Sponsor Protocol Number: BV2012/05 | Start Date*: 2012-09-03 | ||||||||||||||||
Sponsor Name:OM Pharma SA | ||||||||||||||||||
Full Title: Clinical and immune modifying capacity of Broncho-Vaxom® tested by LPS challenge in healthy volunteers A randomized double-blind placebo-controlled trial | ||||||||||||||||||
Medical condition: healthy volunteers intended indication : Experimental induced bronchitis in healthy volunteers | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000620-14 | Sponsor Protocol Number: Cough/1/2010 | Start Date*: 2011-12-22 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA CAREGGI | |||||||||||||
Full Title: Effects of short term Erdosteine treatment on chronic cough on bronchitis phenotypes of COPD | |||||||||||||
Medical condition: COPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003742-15 | Sponsor Protocol Number: 1219.4 | Start Date*: 2008-09-10 |
Sponsor Name:Boehringer Ingelheim France | ||
Full Title: A randomized, double-blind, placebo-controlled, parallel group study to evaluate the safety and efficacy of four weeks treatment of 7.5 mg b.i.d, 15 mg q.d and 15 mg b.i.d. BIBW 2948 BS (inhalation... | ||
Medical condition: Patients with a diagnosis of Chronic Obstructive Pulmonary Diease associated with chronic bronchitis. Patients must be in stable condition and current or ex-smoher. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004167-56 | Sponsor Protocol Number: 027SC06104 | Start Date*: 2007-02-15 | |||||||||||
Sponsor Name:ANGELINI | |||||||||||||
Full Title: Prulifloxacin versus levofloxacin in the treatment of patients with Acute Exacerbations of Chronic Bronchitis AECB | |||||||||||||
Medical condition: Outpatient with acute exacerbations of chronic bronchitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) PT (Completed) ES (Completed) AT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000571-20 | Sponsor Protocol Number: D9180C00002 | Start Date*: 2020-10-09 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase II, Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy, Safety and Tolerability of MEDI3506 in Participants with Moderate to Severe Chronic Obstructive Pulmonary Dise... | |||||||||||||
Medical condition: Moderate to Severe Chronic Obstructive Pulmonary Disease and Chronic Bronchitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) DK (Completed) HU (Completed) NL (Completed) PL (Completed) CZ (Completed) | |||||||||||||
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: 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: 2014-004025-40 | Sponsor Protocol Number: PA101-CC-02 | Start Date*: 2015-02-06 | |||||||||||
Sponsor Name:Patara Pharma | |||||||||||||
Full Title: Treatment of Chronic Idiopathic Cough (CIC) and Chronic Cough in patients with Idiopathic Pulmonary Fibrosis (IPF) with PA101. | |||||||||||||
Medical condition: Chronic Idiopathic Cough and Chronic Cough in Idiopathic Pulmonary Fibrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000531-88 | Sponsor Protocol Number: SP1-2011 | Start Date*: 2011-06-27 |
Sponsor Name:FONDAZIONE IRCCS CA` GRANDA OSPEDALE MAGGIORE POLICLINICO DI MILANO | ||
Full Title: Ceftidoren versus levofloxacin in the treatment of patients with Acute Exacerbations of Chronic Bronchitis (AECB). Multi-centre, open-label, randomised, levofloxacin-controlled, parallel groups s... | ||
Medical condition: EXACERBATION OF CHRONIC BRONCHITIS | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001412-30 | Sponsor Protocol Number: HMR3647A/4020 | Start Date*: 2005-12-02 |
Sponsor Name:Laboratoire Aventis | ||
Full Title: An open-label, randomized, multicenter, clinical study to compare the effects of telithromycin, azithromycin and cefuroxime axetil on the penicillin or macrolide resistance of Streptococcus pneumon... | ||
Medical condition: Patients with acute exacerbation of chronic bronchitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001530-28 | Sponsor Protocol Number: CQBW251X2201 | Start Date*: 2016-05-09 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double blind, placebo controlled study to assess the safety, tolerability, pharmacokinetics and efficacy of multiple doses of QBW251 in patients with COPD. | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (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 (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002938-20 | Sponsor Protocol Number: 13031 | Start Date*: 2013-11-08 |
Sponsor Name:University of Nottingham | ||
Full Title: An open label trial of azithromycin in chronic productive cough | ||
Medical condition: The medical condition that will be investigated is that of chronic productive cough (with or without a diagnosis of asthma but without a diagnosis of bronchiectasis, smoking related chronic bronchi... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001975-40 | Sponsor Protocol Number: 1219.5 | Start Date*: 2007-01-04 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, parallel group study to evaluate the effects of a 4-week treatment of 15 mg b.i.d BIBW 2948 BS (inhalation powder, hard capsule for HandiHaler®) on e... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) patients with symptoms associated with chronic bronchitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008192-34 | Sponsor Protocol Number: ERD-01-08/EP | Start Date*: 2009-08-13 | ||||||||||||||||
Sponsor Name:EDMOND PHARMA S.R.L. | ||||||||||||||||||
Full Title: THE EFFICACY AND SAFETY OF ERDOSTEINE IN THE LONG-TERM THERAPY OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD). A 12-month, randomized, double-blind, placebo-controlled, parallel group, multicenter... | ||||||||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) GB (Completed) CZ (Completed) FR (Completed) DK (Completed) SK (Completed) BE (Completed) BG (Completed) | ||||||||||||||||||
Trial results: View results |
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