- Trials with a EudraCT protocol (798)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
798 result(s) found for: Cough.
Displaying page 1 of 40.
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: 2014-000306-36 | Sponsor Protocol Number: XEN-D0501-CL-04 | Start Date*: 2014-05-20 | |||||||||||
Sponsor Name:Xention Limited | |||||||||||||
Full Title: A double-blind, randomised, placebo-controlled, crossover study to assess the efficacy of XEN D0501, a TRPV1 antagonist, in reducing the frequency of cough in patients with chronic idiopathic cough | |||||||||||||
Medical condition: Chronic Idiopathic Cough | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005074-11 | Sponsor Protocol Number: 14/GAR/002 | Start Date*: 2015-04-29 | |||||||||||
Sponsor Name:University Hospital South Manchester NHS Foundation Trust | |||||||||||||
Full Title: The Role of GABAb receptor mechanisms in cough: Double-blind randomised controlled trial of Lesogaberan in Chronic cough patients with positive and negative symptom association probabilities | |||||||||||||
Medical condition: Chronic cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004136-17 | Sponsor Protocol Number: BUS-P2-02 | Start Date*: 2021-02-05 | |||||||||||
Sponsor Name:Bellus Health Inc. | |||||||||||||
Full Title: A Randomized, Adaptive, Double-Blind, Placebo-Controlled, Parallel-Arm, Phase 2b Study to Evaluate the Efficacy and Safety of Multiple Doses of BLU-5937 in Adult Participants With Refractory Chro... | |||||||||||||
Medical condition: Refractory Chronic Cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) CZ (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005533-38 | Sponsor Protocol Number: ABR 14828 | Start Date*: 2007-06-28 |
Sponsor Name:there is no sponsor. | ||
Full Title: 'Studies in patients with chronic cough; montelukast and amitriptyline studies’. | ||
Medical condition: Chronic cough ( cough lasting > 8 weeks). | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003980-36 | Sponsor Protocol Number: IIT15419 | Start Date*: 2018-01-26 | |||||||||||
Sponsor Name:Hull and East Yorkshire Hospitals NHS Trust | |||||||||||||
Full Title: A single-Centre, open-label, exploratory study of the effect of 20 mg ambroxol hydrochloride on cough reflex sensitivity in patients with acute cough. | |||||||||||||
Medical condition: acute cough assouciated with URTI | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002283-27 | Sponsor Protocol Number: 1812VA323 | Start Date*: 2020-03-18 | |||||||||||
Sponsor Name:Shionogi B.V. | |||||||||||||
Full Title: A phase 2b, multicenter, randomized, double-blind, placebo-controlled, parallel-group, dose selection study of S-600918 in patients with refractory chronic cough | |||||||||||||
Medical condition: Refractory chronic cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003250-16 | Sponsor Protocol Number: MTI-110 | Start Date*: 2017-12-11 | |||||||||||
Sponsor Name:Menlo Therapeutics Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study Of The Efficacy, Safety, And Tolerability Of Serlopitant For The Treatment Of Refractory Chronic Cough | |||||||||||||
Medical condition: Refractory Chronic Cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019647-19 | Sponsor Protocol Number: MAC_001 | Start Date*: 2011-02-04 |
Sponsor Name:University of Oxford | ||
Full Title: A double blind randomised placebo controlled trial of montelukast in the treatment of acute persistent cough in young people and adults (aged 16-49) in primary care | ||
Medical condition: Acute persistent cough with no established diagnosis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-024283-18 | Sponsor Protocol Number: AF219-006 | Start Date*: 2011-05-20 | |||||||||||
Sponsor Name:Afferent Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Study to Assess the Efficacy of AF-219, a P2X3 Receptor Antagonist, in Subjects with Chronic Cough | |||||||||||||
Medical condition: Subjects with Chronic Cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005151-13 | Sponsor Protocol Number: MEM-COUGH-01 | Start Date*: 2012-05-17 | |||||||||||
Sponsor Name:University of Manchester [...] | |||||||||||||
Full Title: Open-label Pilot Study of Memantine in Chronic Cough Patients Attending a Specialist Clinic | |||||||||||||
Medical condition: Idiopathic and treatment resistant Chronic Cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022472-31 | Sponsor Protocol Number: Lidocaine1 | Start Date*: 2010-12-23 |
Sponsor Name:University Hospital of South Manchester | ||
Full Title: The effect of Lidocaine and its Delivery in Patients with Chronic Cough | ||
Medical condition: Chronic Cough | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002308-42 | Sponsor Protocol Number: MK-7264-043 | Start Date*: 2019-12-20 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co.,Inc | |||||||||||||
Full Title: A Phase 3b Randomized, Double-blind, Placebo Controlled, Multicenter Study to Evaluate the Efficacy and Safety of Gefapixant in Adult Participants with Recent Onset Chronic Cough | |||||||||||||
Medical condition: Chronic Cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) PL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004589-14 | Sponsor Protocol Number: BC1036-001 | Start Date*: 2012-05-17 | ||||||||||||||||
Sponsor Name:Respicopea Limited | ||||||||||||||||||
Full Title: A Multicentre, Double-Blind, Placebo-Controlled, Adaptive Pivotal Study of the Efficacy and Safety of Oral BC1036 in the Management of Cough | ||||||||||||||||||
Medical condition: Chronic and sub acute persistent cough | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003947-36 | Sponsor Protocol Number: NT2014/Orv/Prot001 | Start Date*: 2015-01-12 | |||||||||||
Sponsor Name:NeRRe Therapeutics Ltd | |||||||||||||
Full Title: Evaluation of orvepitant in an exploratory open-label clinical study in chronic treatment-refractory cough | |||||||||||||
Medical condition: Chronic treatment-refractory cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011525-13 | Sponsor Protocol Number: V001 | Start Date*: 2009-08-28 | |||||||||||
Sponsor Name:Vernalis (R&D) Limited | |||||||||||||
Full Title: Phase II Open-label Pilot Study of V3381, a Novel N-Methyl-D-Aspartate Receptor Antagonist, in Chronic Cough Patients attending a Specialist Clinic | |||||||||||||
Medical condition: Treatment resistant and Idiopathic Chronic Cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000866-11 | Sponsor Protocol Number: 7164-L-01 | Start Date*: 2004-08-06 | |||||||||||
Sponsor Name:ZAMBON GROUP | |||||||||||||
Full Title: A multicenter, randomized, parallel group, controlled, double-blind study to evaluate efficacy and safety of pholcodine as antitussive agent vs dextrometorphan in non-productive cough | |||||||||||||
Medical condition: Symptomatic treatment of non productive cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
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: 2015-002034-47 | Sponsor Protocol Number: AF219-014 | Start Date*: 2015-10-12 |
Sponsor Name:Afferent Pharmaceuticals, Inc. | ||
Full Title: A Study to Assess the Effect of AF-219 on Cough Reflex Sensitivity in Both Healthy and Chronic Cough Subjects | ||
Medical condition: Chronic cough | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004255-31 | Sponsor Protocol Number: IFH-2014-004 | Start Date*: 2014-12-02 |
Sponsor Name:infirst HEALTHCARE | ||
Full Title: A real world, single-blind, randomised study to compare an OTC cough medicine (cs1002) containing diphenhydramine, levomenthol and ammonium chloride with a simple linctus containing citric acid mon... | ||
Medical condition: acute cough | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
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