- Trials with a EudraCT protocol (11)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
11 result(s) found for: Cough reflex.
Displaying page 1 of 1.
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: 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: 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: 2013-002728-17 | Sponsor Protocol Number: GRC17536-204 | Start Date*: 2013-09-24 | |||||||||||
Sponsor Name:Glenmark Pharmaceuticals SA | |||||||||||||
Full Title: A Phase 2a, Multi-Centre, Randomised, Double-Blind, Parallel Group, Placebo-Controlled Study to Evaluate Efficacy, Safety and Tolerability of Inhaled GRC 17536, Administered for 4 Weeks, in Patient... | |||||||||||||
Medical condition: Refractory Chronic Cough. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000464-34 | Sponsor Protocol Number: AF219-015 | Start Date*: 2015-04-29 |
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: 2006-002165-39 | Sponsor Protocol Number: P04887 | Start Date*: 2006-11-30 |
Sponsor Name:Schering Plough Research Institute, a division of Schering Corporation | ||
Full Title: Study of the Efficacy and Safety of SCH486757 in Subjects With Chronic Idiopathic Cough | ||
Medical condition: Chronic Idiopathic Cough | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-002164-26 | Sponsor Protocol Number: P04888 | Start Date*: 2006-11-10 |
Sponsor Name:Schering Plough Research Institute, a division of Schering Corporation | ||
Full Title: Study of the Efficacy and Safety of SCH619734 in Subjects with Chronic Idiopathic Cough | ||
Medical condition: Chronic Idiopathic Cough | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001736-38 | Sponsor Protocol Number: Academed100215 | Start Date*: 2015-08-26 |
Sponsor Name:Hull and East Yorkshire Hospitals NHS trust | ||
Full Title: The utility of feNO in the differential diagnosis of chronic cough: The response to anti-inflammatory therapy with prednisolone and montelukast | ||
Medical condition: Chronic cough is a common and poorly diagnosed condition. Younger patients tend to receive a diagnosis of asthma, whereas older patients are increasingly identified has having gastroesophageal refl... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-004463-39 | Sponsor Protocol Number: 221921 | Start Date*: 2019-03-06 |
Sponsor Name:Sahlgrenska University Hospital, Department of Internal Medicine/Respiratory Medicine and Allergology [...] | ||
Full Title: Influence on cough and airway symptoms by oral capsaicin (capscium oleoresin ) – a phase II, randomised, placebo-controlled clinical study in patients with chronic idiopathic cough | ||
Medical condition: Chronic idiopathic cough | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004891-20 | Sponsor Protocol Number: PNV117270 | Start Date*: 2013-09-06 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
Full Title: A randomised, double-blind (sponsor-unblind), placebo controlled, cross-over study to investigate the efficacy, effect on cough reflex sensitivity, safety, tolerability and pharmacokinetics of inha... | |||||||||||||
Medical condition: chronic idiopathic cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004744-31 | Sponsor Protocol Number: TR12 | Start Date*: 2019-06-24 |
Sponsor Name:Trevi Therapeutics, Inc. | ||
Full Title: A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Two-Treatment, Two-Period Crossover Efficacy and Safety Study in Idiopathic Pulmonary Fibrosis With Nalbuphine ER Tablets for the Treatment ... | ||
Medical condition: Treatment of Cough in Idiopathic Pulmonary Fibrosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
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