- Trials with a EudraCT protocol (198)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (8)
198 result(s) found for: Chronic bronchitis.
Displaying page 1 of 10.
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: 2007-005637-11 | Sponsor Protocol Number: BV-2007/06 | Start Date*: 2008-08-04 | |||||||||||
Sponsor Name:OM Pharma SA | |||||||||||||
Full Title: Efficacy of Broncho-Vaxom in elderly patients with chronic bronchitis; a double-blind, randomised, placebo-controlled study | |||||||||||||
Medical condition: Chronic bronchitis | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017872-26 | Sponsor Protocol Number: 1147/09 | Start Date*: 2010-02-22 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Role and pharmacological modulation of lug inflammation in chronic obstructive pulmonary disease (COPD) | |||||||||||||
Medical condition: chronic obstructive pulmonary disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (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: 2007-004869-18 | Sponsor Protocol Number: 030547 | Start Date*: 2008-07-03 | ||||||||||||||||||||||||||
Sponsor Name:UHB NHS Foundation Trust | ||||||||||||||||||||||||||||
Full Title: Evaluation of the relative severity of pulmonary neutrophilic inflammation and therapeutic modification with IV Prolastin by means of 18 FDG PET/CT scanning in subjects with alpha1-antitrypsin defi... | ||||||||||||||||||||||||||||
Medical condition: The medical condition is emphysema and will be investigated in subjects with alpha 1-antitrypsin deficiency. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-001749-42 | Sponsor Protocol Number: 484/12 | Start Date*: 2012-08-07 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Effects of treatment and withdrawal with inhaled beclomethasone/formoterol on lung inflammation in COPD. | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (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: 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: 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: 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: 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: 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: 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: 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: 2006-004048-21 | 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: 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: 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: 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: 2020-000210-15 | Sponsor Protocol Number: ION-827359-CS2 | Start Date*: 2020-10-08 | |||||||||||
Sponsor Name:Ionis Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Double-Blind, Placebo-Controlled, Phase 2a Study to Assess the Safety, Tolerability, and Efficacy of ION-827359 in Patients with Mild to Moderate COPD with Chronic Bronchitis | |||||||||||||
Medical condition: Mild to Moderate Chronic obstructive pulmonary disease (COPD) with Chronic Bronchitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Prematurely Ended) HU (Prematurely Ended) CZ (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013763-19 | Sponsor Protocol Number: CQAB149BIT01 | Start Date*: 2009-09-24 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: Multicenter, randomized, blinded, placebo controlled, cross over, single dose study to assess the effect of indacaterol (150 �g) versus tiotropium (18 �g) on Inspiratory Capacity in moderate COPD p... | |||||||||||||
Medical condition: moderate COPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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