- Trials with a EudraCT protocol (27)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
27 result(s) found for: Mouthwash.
Displaying page 1 of 2.
EudraCT Number: 2013-002708-14 | Sponsor Protocol Number: OML0113 | Start Date*: 2013-10-09 | |||||||||||
Sponsor Name:Schülke & Mayr GmbH | |||||||||||||
Full Title: Phase II study to assess bacterial count reduction of three Octenidine mouthwash concentrations in comparison to a placebo in patients with mild gingivitis | |||||||||||||
Medical condition: patients aged 18 and older with mild gingivitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000869-20 | Sponsor Protocol Number: DC0071-BB-404-8B | Start Date*: 2005-08-08 |
Sponsor Name:Pierre Fabre Médicament | ||
Full Title: Post-operative care by chlorhexidine mouthwash after periodontal surgery. Randomised, parallel groups; blind study, DC071BB versus placebo, in patients presenting with periodontal surgery with sutu... | ||
Medical condition: Post-operative care for patients having periodontal surgery with gingival suture. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) EE (Completed) LV (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-001697-42 | Sponsor Protocol Number: OML-III-A | Start Date*: 2017-08-30 | |||||||||||
Sponsor Name:Schülke & Mayr GmbH | |||||||||||||
Full Title: Randomized, placebo-controlled, parallel group, double-blind, multi-center Phase III study to assess the inhibition of plaque formation of 0.1% octenidine mouthwash vs placebo in subjects with a gi... | |||||||||||||
Medical condition: inhibition of plaque formation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001698-18 | Sponsor Protocol Number: OML-III-B | Start Date*: 2017-11-06 | |||||||||||
Sponsor Name:Schülke & Mayr GmbH | |||||||||||||
Full Title: Randomized, placebo-controlled, parallel group, double-blind, multi-center Phase III study to assess the inhibition of plaque formation of 0.1% octenidine mouthwash vs placebo in subjects with a gi... | |||||||||||||
Medical condition: inhibition of plaque formation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003604-12 | Sponsor Protocol Number: ITM201902 | Start Date*: 2020-01-15 | |||||||||||
Sponsor Name:Institute of Tropical Medicine | |||||||||||||
Full Title: Evaluation of a chlorhexidine mouthwash for the eradication of asymptomatic pharyngeal Neisseria gonorrhoeae infection | |||||||||||||
Medical condition: asymptomatic pharyngeal Neisseria gonorrhoeae (NG) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004222-28 | Sponsor Protocol Number: LIKLO1 | Start Date*: 2020-03-23 | |||||||||||
Sponsor Name:Malmö University | |||||||||||||
Full Title: Efficacy of topical treatment with clobetasol in symptomatic oral lichen planus. A multicenter placebo-controlled randomized clinical trial. | |||||||||||||
Medical condition: Oral lichen planus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002418-11 | Sponsor Protocol Number: RH01913 | Start Date*: 2013-08-12 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Consumer Healthcare | ||||||||||||||||||
Full Title: A study to evaluate the effect of a 67% Sodium Bicarbonate containing toothpaste on Chlorhexidine Digluconate tooth staining | ||||||||||||||||||
Medical condition: Tooth discolouration (a labelled undesirable effect of Corsodyl 0.2% mouthwash) | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2013-003548-22 | Sponsor Protocol Number: LAEBBA0005 | Start Date*: 2014-03-03 |
Sponsor Name:Johnson & Johnson Consumer & Personal Products Worldwide, Division of Johnson & Johnson Consumer Companies, Inc | ||
Full Title: Four Week Clinical Efficacy of An Ethyl Lauroyl Arginate HCL (LAE) Mouth Rinse: Effect on Gingivitis | ||
Medical condition: Gingivitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-003306-32 | Sponsor Protocol Number: 030(Z)WO19247 | Start Date*: 2021-01-18 | |||||||||||
Sponsor Name:Angelini Pharma S.p.A. | |||||||||||||
Full Title: Phase IV study on the feasibility of a preventative/therapeutic approach with Benzydamine Oromucosal solution in radiation-induced Oral Mucositis (OM) in patients with head and neck cancer (HNC) | |||||||||||||
Medical condition: Oral Mucositis (OM) in patients with head and neck cancer (HNC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004682-24 | Sponsor Protocol Number: DC0071BB405 | Start Date*: 2015-04-27 | |||||||||||
Sponsor Name:Institut de Recherche Pierre Fabre - Centre de R&D Pierre Fabre | |||||||||||||
Full Title: Efficacy of DC071 mouthwash (0,2 % chlorhexidine digluconate) in peri-surgical care for preventing alveolar osteitis after third molar extraction. Prospective, multicenter, randomised, double-blin... | |||||||||||||
Medical condition: Prevention of alveolar osteitis after third molar extraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) LV (Completed) LT (Completed) FR (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002236-87 | Sponsor Protocol Number: RH01561 | Start Date*: 2012-08-16 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Consumer Healthcare | ||||||||||||||||||
Full Title: Clinical Study to Evaluate the Efficacy of Chlorhexidine Mouthwashes | ||||||||||||||||||
Medical condition: Gingival bleeding and gingivitis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-002698-65 | Sponsor Protocol Number: 05_DOG13_71 | Start Date*: 2006-04-10 |
Sponsor Name:Christie Hospital NHS Trust | ||
Full Title: A randomised clinical trial comparing safety and efficacy of topical preparations for the eradication of methicillin resistant staphylococcus aureus (MRSA) compared with a novel preparation based o... | ||
Medical condition: Colonisation with methicillin resistant Staphylococcus Aureus (MRSA) | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-001426-17 | Sponsor Protocol Number: 1M | Start Date*: 2018-01-03 |
Sponsor Name:University Hospitals Leuven (Gasthuisberg) | ||
Full Title: Tranexamic Acid to reduce bleeding in patients treated with new oral anticoagulants undergoing dental extraction (EXTRACT-NOAC) | ||
Medical condition: Patients treated with a NOAC, aged 18 years or older undergoing dental extraction | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-000260-17 | Sponsor Protocol Number: Intermed_Chlorhexidine_sol_0.2%_ | Start Date*: 2012-09-07 | |||||||||||||||||||||
Sponsor Name:IOULIA & IRENE TSETI PHARMACEUTICAL LABORATORIES S.A.-INTERMED S.A. | |||||||||||||||||||||||
Full Title: A therapeutic equivalence study, comparing two chlorhexidine digluconate formulations, the test formulation Chlorel® Or. T. Sol. 0,2% w / v and the reference formulation Corsodyl® 0.2% w / v Mint M... | |||||||||||||||||||||||
Medical condition: Therapeutic equivalence study, comparing two chlorhexidine digluconate formulations indicated for inhibition of the formation of dental plaque, as an aid in the treatment and prevention of gingivi... | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-003260-53 | Sponsor Protocol Number: 102010 | Start Date*: 2006-07-24 | |||||||||||
Sponsor Name:Danmarks Farmaceutiske Universitet | |||||||||||||
Full Title: Lokal administration af morfin: Evaluering af den smertestillende effekt på stomatitis hos børn. | |||||||||||||
Medical condition: Stomatitis som bivirkning til kemoterapi. | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002624-15 | Sponsor Protocol Number: FERTOMCIDINA | Start Date*: 2007-06-28 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
Full Title: Fertomcidina モUヤ vs chlorhexidine 0.2% in recurrent aphthous stomatitis: randomized comparative double-blind study. | |||||||||||||
Medical condition: patients with recurrent aphthous stomatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004825-42 | Sponsor Protocol Number: Notapplicablenow | Start Date*: 2016-12-22 |
Sponsor Name:ACTA | ||
Full Title: Effect of Delmopinol on treatment of Peri - implant mucositis : a randomised controlled clinical trial | ||
Medical condition: Peri implant mucositis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001721-31 | Sponsor Protocol Number: SPON-AK-0420 | Start Date*: 2020-05-01 | |||||||||||
Sponsor Name:Hampshire Hospitals NHS TRust | |||||||||||||
Full Title: Can a sinus rinse and mouth wash reduce viral load in COVID-19 positive individuals? | |||||||||||||
Medical condition: Covid-19 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003327-36 | Sponsor Protocol Number: ART1 | Start Date*: 2007-01-08 |
Sponsor Name:Guy's & St Thomas' NHS Foundation Trust [...] | ||
Full Title: Evaluation of the efficacy of colchicine with and without betamethasone mouthwash in the management of recurrent aphthous stomatitis | ||
Medical condition: Recurrent aphthous stomatitis (RAS) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004760-31 | Sponsor Protocol Number: CG/7657 | Start Date*: 2007-04-17 | |||||||||||
Sponsor Name:University of Dundee | |||||||||||||
Full Title: Role and efficacy of topical 5-Aminolevulinic Acid (5-ALA) in Photodynamic detection (PDD) in determining malignant potential of oral lichen planus | |||||||||||||
Medical condition: Oral Lichen Planus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
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