- Trials with a EudraCT protocol (16)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
16 result(s) found for: Throat lozenges.
Displaying page 1 of 1.
EudraCT Number: 2019-003257-29 | Sponsor Protocol Number: 030(Z)WO19176 | Start Date*: 2020-02-25 |
Sponsor Name:Angelini S.p.A. | ||
Full Title: Phase IV study comparing the efficacy and safety of Benzydamine hydrochloride 0,3% oromucosal spray and Benzydamine hydrochloride 3 mg lozenges in patients with acute sore throat. | ||
Medical condition: acute sore throat | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) PL (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-003285-20 | Sponsor Protocol Number: 030(Z)MD22061 | Start Date*: 2023-03-13 | |||||||||||
Sponsor Name:Angelini Pharma S.p.A. | |||||||||||||
Full Title: Phase IV study comparing the efficacy and safety of an alcohol-free formulation of 0.15% benzydamine hydrochloride spray and benzydamine hydrochloride 3mg lozenges in paediatric patients (6-12 year... | |||||||||||||
Medical condition: acute sore throat | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005059-67 | Sponsor Protocol Number: TH0809 | Start Date*: 2008-11-04 | |||||||||||
Sponsor Name:Reckitt Benckiser Healthcare UK Ltd | |||||||||||||
Full Title: A multi-centre, randomised, double blind, placebo-controlled, parallel group, single dose, pilot study of the efficacy of 0.6 mg Amylmetacresol BP (AMC) and 1.2mg 2,4-Dichlorobenzyl alcohol (DCBA) ... | |||||||||||||
Medical condition: Sore throat | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002876-15 | Sponsor Protocol Number: MCMK0112 | Start Date*: 2012-11-23 |
Sponsor Name:Cassella-med GmbH & Co KG | ||
Full Title: A randomised, multi-centre, parallel group, double-blind, placebo- and active-controlled clinical study to assess the efficacy and safety of Octenidine lozenges in the treatment of acute sore throat. | ||
Medical condition: Acute pharyngitis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004423-20 | Sponsor Protocol Number: V00498TA301 | Start Date*: 2013-01-10 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
Full Title: STUDY OF EFFICACY AND SAFETY OF V0498 VERSUS PLACEBO IN ACUTE SORE THROAT PAIN | |||||||||||||
Medical condition: Acute sore throat | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) LV (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021653-39 | Sponsor Protocol Number: 075-A-301 | Start Date*: 2010-12-08 | ||||||||||||||||
Sponsor Name:Novartis Consumer Health S.A. | ||||||||||||||||||
Full Title: A randomized, double-blind, parallel group, single-dose study of the efficacy of lidocaine 8 mg + cetylpyridinium chloride (CPC) 2 mg fixed combination lozenges on sore throat pain intensity compar... | ||||||||||||||||||
Medical condition: Sore throat due to upper respiratory tract infection (Planned indication for approval: Local antiseptic and analgesic treatment of sore throat and minor infections of the mouth. Relief of pain as ... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-004375-19 | Sponsor Protocol Number: TH0705 | Start Date*: 2007-10-26 | |||||||||||
Sponsor Name:Reckitt Benckiser Healthcare | |||||||||||||
Full Title: A multi-centre, randomised, double-blind, parallel-group, placebo-controlled, multiple dose study of the efficacy of Strepsils original throat lozenges in the relief of sore throat due to upper res... | |||||||||||||
Medical condition: Sore throat | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005596-10 | Sponsor Protocol Number: TH0817 | Start Date*: 2008-12-05 | |||||||||||
Sponsor Name:Reckitt Benkiser Healthcare (UK) Ltd | |||||||||||||
Full Title: A multi centre, randomised, double blind, placebo-controlled, parallel group, single dose study of the efficacy of two flavour variants of Strepsils throat lozenges in the relief of sore throat due... | |||||||||||||
Medical condition: Sore Throat | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005095-17 | Sponsor Protocol Number: EA041999 | Start Date*: 2005-02-10 |
Sponsor Name:Engelhard Arzneimittel GmbH & Co. KG | ||
Full Title: Randomised, double-blind, placebo-controlled, monocentric phase III study on the efficacy and safety of Lidocaine 8 mg Sore Throat Lozenges in patients with moderate to severe acute sore throat not... | ||
Medical condition: The study will be performed in patients suffering from acute sore throat not necessarily to be treated with antibiotics | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-008265-36 | Sponsor Protocol Number: KETOP_C_03968 | Start Date*: 2009-05-26 | |||||||||||
Sponsor Name:SANOFI-AVENTIS GROUPE | |||||||||||||
Full Title: “A randomised, double-blind, placebo-controlled, parallel-group study of the efficacy and safety of two doses of ketoprofen lysinate lozenges (6.25mg and 12.5mg ) in patients with sore throat” | |||||||||||||
Medical condition: upper respiratory illness : sore throat | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) FR (Completed) DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005848-10 | Sponsor Protocol Number: V00498TA201 | Start Date*: 2012-02-06 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
Full Title: Analgesic profile of 3 new Ibuprofen lozenges (V0498TA01A 15mg, 25mg, 35mg) after single administration in acute sore throat pain | |||||||||||||
Medical condition: Acute sore throat | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000278-74 | Sponsor Protocol Number: KKL022010 | Start Date*: 2011-07-11 | ||||||||||||||||
Sponsor Name:KRKA, tovarna zdravil, d. d., Novo mesto | ||||||||||||||||||
Full Title: A COMPARATIVE EFFICACY AND SAFETY OF CETYLPYRIDINIUM CHLORIDE 1.0 mg/BENZYDAMINE HYDROCHLORIDE 3 mg FIXED COMBINATION LOZENGES IN SUBJECTS WITH SORE THROAT ASSOCIATED WITH UPPER RESPIRATORY TRACT I... | ||||||||||||||||||
Medical condition: Sore throat associated with upper respiratory infections | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SI (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-024045-69 | Sponsor Protocol Number: TH1017 | Start Date*: 2011-01-11 | |||||||||||
Sponsor Name:Reckitt Benckiser Healthcare | |||||||||||||
Full Title: A multi centre, randomised, double blind, single dose parallel group, placebo controlled study to investigate the efficacy of Strepsils Plus and Strepsils Extra in the treatment of sore throat due ... | |||||||||||||
Medical condition: Sore throat due to upper respiratory tract infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003111-38 | Sponsor Protocol Number: 6630-9050-03 | Start Date*: 2015-12-30 |
Sponsor Name:Medice Arzneimittel Pütter GmbH & Co. KG | ||
Full Title: A double-blind, randomized, placebo-controlled, parallel-group study comparing safety and efficacy of Dorithricin® lozenges with placebo in the symptomatic treatment of patients with acute pharyngitis | ||
Medical condition: Acute pharyngitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003962-24 | Sponsor Protocol Number: 6632-9050-04 | Start Date*: 2016-12-27 |
Sponsor Name:Medice Arzneimittel Pütter GmbH & Co. KG | ||
Full Title: A multi-centre, randomized, placebo-controlled, double-blind, parallel-group study investigating safety and efficacy of a sore throat lozenge in the symptomatic treatment of patients with acute pha... | ||
Medical condition: Acute Pharyngitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003588-22 | Sponsor Protocol Number: TH0504 | Start Date*: 2005-11-29 |
Sponsor Name:Boots Healthcare International Limited | ||
Full Title: A single centre, randomised, single (patient) blind, single dose, parallel group exploratory study to compare the efficacy of an 8.75mg flurbiprofen lozenge (Strefen) with a 3mg benzydamine lozenge... | ||
Medical condition: Sore throat suitable for treatment in an OTC setting. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
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