- Trials with a EudraCT protocol (18)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
18 result(s) found for: Gingivitis.
Displaying page 1 of 1.
EudraCT Number: 2008-008512-51 | Sponsor Protocol Number: ONE-GLY-P2-01 | Start Date*: 2009-06-09 | |||||||||||
Sponsor Name:onepharm Research & Development GmbH | |||||||||||||
Full Title: A double blind, randomized, placebo-controlled, three-arm, phase II study to investigate the safety and efficacy of oral glycyrrhizin (Glycyron® tablets) for the treatment of gingivitis | |||||||||||||
Medical condition: patients with gingivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2009-015914-23 | Sponsor Protocol Number: T3450515 | Start Date*: 2009-12-24 | |||||||||||
Sponsor Name:GlaxoSmithKline Consumer Healthcare (GSKCH) | |||||||||||||
Full Title: Clinical efficacy of an experimental toothpaste | |||||||||||||
Medical condition: Gingivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
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: 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: 2008-002982-30 | Sponsor Protocol Number: AGO/2008/004 | Start Date*: 2008-10-09 |
Sponsor Name:University Hospital Ghent | ||
Full Title: A Prospective, randomized, clinical study on the effects of CPP-ACP paste on plaque, gingivitis and initial caries lesion development in orthodontic patients - part 2 | ||
Medical condition: Plaque and the initial development of caries and gingivitis in orthodontic patients. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000990-39 | Sponsor Protocol Number: V00109 DI 301 | Start Date*: 2008-05-22 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
Full Title: Reduction of the gingival inflammation by V0109 DI. Randomised, parallel groups, double blind study, V0109 DI versus placebo, in patients presenting gingivitis. | |||||||||||||
Medical condition: Reduction of the gingival inflammation by V0109 DI. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) LV (Completed) | |||||||||||||
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: 2006-002192-40 | Sponsor Protocol Number: periodld001 | Start Date*: 2006-07-13 |
Sponsor Name:Zsolt Lohinai DMD PhD | ||
Full Title: New treatment of periodontitis by inhibition of lysine decarboxilase enzyme | ||
Medical condition: healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
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: 2013-002190-22 | Sponsor Protocol Number: Phlogosol_2013/01 | Start Date*: 2014-03-26 |
Sponsor Name:PannonPharma Ltd. | ||
Full Title: Therapeutic clinical trial of three types of “Phlogosol concentrate for gargle” products, comparing their efficacy in reducing different inflammations of the oral cavity. (Changing the active ing... | ||
Medical condition: Cold with sore throat, acute stomatitis, chronic pharyngitis acute tonsillitis, acute laryngitis, herpes stomatitis, superficial glossitis, acute and chronic gingivitis, ulcerative gingivitis, paro... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-003430-16 | Sponsor Protocol Number: OC004PDS | Start Date*: 2012-11-15 | |||||||||||
Sponsor Name:Clinical Reasearch Centre, Hvidovre University Hospital | |||||||||||||
Full Title: Effect of local anesthesia in patients with marginal periodontitis undergoing subgingival scaling | |||||||||||||
Medical condition: Pain and discomfort during dental treatment in patients with periodontitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001367-36 | Sponsor Protocol Number: DoxP-01/2006 | Start Date*: 2006-12-05 | |||||||||||
Sponsor Name:Prof. Dr. Peter Eickholz | |||||||||||||
Full Title: Benefit of adjunctive systemic postsurgical doxycycline in regenerative periodontal surgery | |||||||||||||
Medical condition: Periodontitis is an opportunistic infectious disease that destroys the periodontal attachment and bone. Bacterial plaque (biofilm) on the teeth adjacent to the gingiva is the necessary cause gingiv... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005953-31 | Sponsor Protocol Number: STAB 1 | Start Date*: 2007-05-03 |
Sponsor Name:GlaxoSmithKline Consumer Healthcare GmbH & Co. KG | ||
Full Title: Inhibition of Dental Plaque Regrowth by an Ethanol-Free 0,2% Chlorhexidine Mouth Rinsing Solution | ||
Medical condition: The purpose of this study is to examine the inhibitory effect of an ethanol-free 0,2% chlorhexidine digluconate (CHX) mouthrinse on the bacterial plaque growth after professional tooth cleaning in ... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-000973-24 | Sponsor Protocol Number: EK-NM-01-05 | Start Date*: 2005-06-14 | |||||||||||
Sponsor Name:ERREKAPPA EUROTERAPICI | |||||||||||||
Full Title: Nimesulide spray in the treatment of simpthomatic inflammation with pain of the oral cavity (faringitis, stomatitis, pharyngitis) pre e post dental extraction. Randomised controlled vs active drug... | |||||||||||||
Medical condition: DISEASES OF UPPER RESPIRATORY TRACT (GINGIVITIS; PHARYNGITIS; STOMATITIS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000712-59 | Sponsor Protocol Number: APHP200073 | Start Date*: 2023-03-14 | |||||||||||
Sponsor Name:Assistance Publique - Hôpitaux Paris (Direction de la Recherche Clinique et de l’Innovation) | |||||||||||||
Full Title: Severe erythema multiforme: A randomized controlled trial comparing a short systemic corticosteroids regimen to placebo in the acute established phase | |||||||||||||
Medical condition: Erythema multiforme (EM) in its severe form managed at the hospital | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019060-37 | Sponsor Protocol Number: CH.MAX-FACC.02/2009 | Start Date*: 2010-07-09 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | ||||||||||||||||||
Full Title: Clinical prospective study to evaluate the efficacy of hygienical therapy and metronidazole in addition to antibiotic therapy in patients affected by bisphosponate-associated osteonecrosis of the jaws | ||||||||||||||||||
Medical condition: patients affected by bisphosponate-associated osteonecrosis of the jaws and infection. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000600-29 | Sponsor Protocol Number: UX023-CL301 | Start Date*: 2016-09-15 | |||||||||||
Sponsor Name:Ultragenyx Pharmaceuticals Inc | |||||||||||||
Full Title: A Randomized, Open-Label, Phase 3 Study to Assess the Efficacy and Safety of KRN23 Versus Oral Phosphate and Active Vitamin D Treatment in Pediatric Patients with X-linked Hypophosphatemia (XLH) | |||||||||||||
Medical condition: X-linked hypophosphatemia (XLH) is a disorder of renal phosphate wasting, defective bone mineralisation, and impaired growth plate or endochondral ossification caused by inactivating mutations in t... | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) IE (Completed) DE (Completed) ES (Prematurely Ended) SE (Completed) GB (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
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