- Trials with a EudraCT protocol (80)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
80 result(s) found for: Bronchiectasis.
Displaying page 1 of 4.
EudraCT Number: 2009-009869-34 | Sponsor Protocol Number: BAYq3939/12965 | Start Date*: 2009-06-08 | ||||||||||||||||
Sponsor Name:Bayer HealthCare AG | ||||||||||||||||||
Full Title: Randomized, placebo-controlled, double-blind, multi center study to evaluate the safety and efficacy of ciprofloxacin inhale compared to placebo in patients with non-cystic fibrosis bronchiectasis | ||||||||||||||||||
Medical condition: Idiopathic and post-pneumonic non-Cystic Fibrosis Bronchiectasis in pulmonary stable patients (defined as FEV1 of > 35 % and < 80 percent of predicted) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) ES (Completed) SE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-021472-28 | Sponsor Protocol Number: D3550C00014 | Start Date*: 2011-01-10 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase II Randomised, Double-blind, Placebo-controlled, Parallel Group Study to Assess the efficacy of 28-Day Oral Administration of AZD5069 Twice Daily in Patients with Bronchiectasis. | |||||||||||||
Medical condition: Bronchiectasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000936-21 | Sponsor Protocol Number: 2007LF004B | Start Date*: 2007-09-10 | |||||||||||
Sponsor Name:Royal Brompton | |||||||||||||
Full Title: THE EFFECT ON ALVEOLAR NITRIC OXIDE OF SALMETEROL, FLUTICASONE, AND IN COMBINATION, IN STABLE BRONCHIECTASIS. | |||||||||||||
Medical condition: bronchiectasis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000753-35 | Sponsor Protocol Number: D0520C00010 | Start Date*: 2009-02-20 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase II, Randomised, Double-Blind, Placebo-Controlled, Parallel Group Study to Assess the Efficacy of 28 Day Oral Administration of AZD9668 in Patients with Bronchiectasis | |||||||||||||
Medical condition: Bronchiectasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022040-20 | Sponsor Protocol Number: Statin_2010 | Start Date*: 2010-12-17 | |||||||||||
Sponsor Name:NHS Lothian [...] | |||||||||||||
Full Title: A Randomised Controlled Trial of Atorvastatin as an Anti-Inflammatory Agent in Non-Cystic Fibrosis Bronchiectasis | |||||||||||||
Medical condition: The aim of this randomised double blind controlled study to evaluate the efficacy of 6 months treatment with atorvastatin versus placebo in patients with clinically significant bronchiectasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023959-28 | Sponsor Protocol Number: GS-US-219-0104 | Start Date*: 2011-07-04 | ||||||||||||||||
Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
Full Title: A Phase 3, Double-Blind, Multicenter, Randomized, Placebo-Controlled Trial Evaluating Repeated Courses of Aztreonam for Inhalation Solution/Aztreonam 75 mg Powder and Solvent for Nebuliser Solutio... | ||||||||||||||||||
Medical condition: Non-CF bronchiectasis and gram-negative endobronchial infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) BE (Completed) NL (Completed) ES (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-001541-40 | Sponsor Protocol Number: Pro12/15 | Start Date*: 2012-08-20 | |||||||||||
Sponsor Name:Vu University Medical Center | |||||||||||||
Full Title: Effect of Carbon Dioxide Enriched Ambient Air on Pharmacokinetics and Deposition In Bronchiectasis Patients Using Tobramycin Inhalation: A proof of concept study. | |||||||||||||
Medical condition: Bronchiectasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003304-41 | Sponsor Protocol Number: 1397-0012 | Start Date*: 2022-06-09 | |||||||||||
Sponsor Name:Boehringer Ingelheim SComm | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, parallel group, dose-finding study evaluating efficacy, safety and tolerability of BI 1291583 qd over at least 24 weeks in patients with bronchiectas... | |||||||||||||
Medical condition: bronchiectasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Completed) ES (Completed) HU (Completed) FR (Completed) IT (Completed) LV (Completed) CZ (Completed) DE (Completed) GR (Completed) DK (Completed) PL (Completed) PT (Completed) BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001590-24 | Sponsor Protocol Number: 01.01.18 | Start Date*: 2019-03-21 | |||||||||||
Sponsor Name:University of Dundee [...] | |||||||||||||
Full Title: A Trial of the Safety, Tolerability and Efficacy of 2 doses of Cayston (Aztreonam Lysine) compared to placebo in participants with bronchiectasis. | |||||||||||||
Medical condition: Bronchiectasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002644-42 | Sponsor Protocol Number: DPM-B-305 | Start Date*: 2008-07-15 | |||||||||||
Sponsor Name:Pharmaxis Pharmaceuticals Limited | |||||||||||||
Full Title: A phase III multicenter, randomized, parallel, controlled, double blind study to investigate the safety and efficacy of inhaled mannitol over 12 months in the treatment of bronchiectasis | |||||||||||||
Medical condition: Bronchiectasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001026-62 | Sponsor Protocol Number: ETGOL | Start Date*: 2021-10-05 | |||||||||||
Sponsor Name:University Hospital Dr Josep Trueta | |||||||||||||
Full Title: Benefits of inhalation of 7% hypertonic saline solution prior to ELTGOL physiotherapy, in patients with bronchiectasis. A randomized controlled trial. | |||||||||||||
Medical condition: bronchiectasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022042-24 | Sponsor Protocol Number: Statin_p.aeruginosa | Start Date*: 2010-12-24 | |||||||||||
Sponsor Name:NHS Lothian [...] | |||||||||||||
Full Title: A Randomised Controlled Trial of Atorvastatin as an Anti-Inflammatory Agent in Non-Cystic Fibrosis Bronchiectasis in patients with Pseudomonas Aeruginosa | |||||||||||||
Medical condition: The aim of this randomized double blind controlled study is to evaluate the efficacy of a 3 months treatment with atorvastatin versus placebo in patients with clinically significant bronchiectasis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002792-34 | Sponsor Protocol Number: Bronch | Start Date*: 2014-02-26 | |||||||||||
Sponsor Name:University Hospitals Leicester NHS Trust | |||||||||||||
Full Title: Phenotyping bronchiectasis based on aetiology, exacerbation characteristics and response to erythromycin. | |||||||||||||
Medical condition: Bronchiectasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008731-28 | Sponsor Protocol Number: DPM-B-305 | Start Date*: 2009-06-05 |
Sponsor Name:Pharmaxis Pharmaceuticals Limited | ||
Full Title: A phase III multicentre, randomized, parallel, controlled, double blind study to investigate the safety and efficacy of inhaled mannitol over 12 months in the treatment of bronchiectasis. | ||
Medical condition: Bronchiectasis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) NL (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-000264-17 | Sponsor Protocol Number: ARD-3100-0703 | Start Date*: 2008-08-19 | |||||||||||
Sponsor Name:Aradigm Corporation | |||||||||||||
Full Title: A MULTI-CENTER, OPEN-LABEL, PROOF-OF-CONCEPT STUDY TO EVALUATE THE SAFETY, TOLERABILITY, AND EFFECT ON SPUTUM PSEUDOMONAS AERUGINOSA DENSITY OF INHALED LIPOSOMAL CIPROFLOXACIN HYDROCHLORIDE IN ADUL... | |||||||||||||
Medical condition: To evaluate the safety, tolerability, and effect on sputum P. aeruginosa density of two dose levels of liposomal ciprofloxacin hydrochloride for inhalation in adult subjects with non-CF bronchiecta... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005045-34 | Sponsor Protocol Number: PPCTP/001 | Start Date*: 2008-12-15 | |||||||||||
Sponsor Name:Profile Pharma Ltd | |||||||||||||
Full Title: A double-blind, vehicle-controlled, multi-centre, clinical study to investigate the efficacy and safety of up to 6 months of therapy with inhaled Promixin in the treatment of patients with non-cyst... | |||||||||||||
Medical condition: non-CF bronchiectasis (CF = cystic fibrosis) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003023-22 | Sponsor Protocol Number: 2014-26 | Start Date*: Information not available in EudraCT |
Sponsor Name:ASSISTANCE PUBLIQUE HOPITAUX DE MARSEILLE | ||
Full Title: Open trial with randomized withdrawal of treatment, to evaluate the efficacy of azithromycin in the treatment of bronchiectasis excluding cystic fibrosis in children (AZI-STOP study) | ||
Medical condition: bronchiectasis excluding cystic fibrosis in children | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004437-16 | Sponsor Protocol Number: tobra-02 | Start Date*: 2013-05-15 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Pharmacokinetic evaluation and tolerability of dry powder tobramycin by a novel device in patients with non cystic fibrosis bronchiectasis | ||
Medical condition: Bronchiectasis Lung infections | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000664-14 | Sponsor Protocol Number: 16178SE-AS | Start Date*: 2018-02-06 |
Sponsor Name:Belfast Health and Social Care Trust | ||
Full Title: A 2x2 factorial randomised examiner blind open label trial to determine the CLinical and cost- Effectiveness of hypertonic saline (HTS 6%) and carbocisteine for Airway cleaRance versus usual care o... | ||
Medical condition: Bronchiectasis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002335-33 | Sponsor Protocol Number: KKS287 | Start Date*: 2022-05-18 | |||||||||||
Sponsor Name:Philipps University Marburg | |||||||||||||
Full Title: Inhaled ColiFin® in adult bronchiectasis patients with new asymptomatic Pseudomonas aeruginosa infection– an open-label, proof of concept - randomized controlled trial | |||||||||||||
Medical condition: bronchiectasis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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