- Trials with a EudraCT protocol (47)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
47 result(s) found for: Gingival.
Displaying page 1 of 3.
| 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: 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: 2005-001885-14 | Sponsor Protocol Number: HN010/HTF-003 | Start Date*: 2005-08-24 |
| Sponsor Name:Henogen s.a. | ||
| Full Title: A phase II, randomised, double blind, matched pair, controlled study to assess the safety and efficacy of Henogen recombinant soluble human tissue factor (rshTF) on the mandible bone consolidation... | ||
| Medical condition: Orthognathic surgery, cases of Bilateral Sagittal Split Osteotomy (B.S.S.O) of the mandible to achieve facial and occlusal balance. This could create bone gaps or continuity defects. These bone gap... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| 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: 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: 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: 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: 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: 2017-002532-16 | Sponsor Protocol Number: 02 | Start Date*: 2017-12-05 |
| Sponsor Name:Cliniques Universitaires Saint-Luc | ||
| Full Title: Adjunctive systemic antimicrobial therapy in the surgical treatment of peri-implantitis. A prospective randomized clinical study | ||
| Medical condition: To treat patients with chronic infection of dental implants. One group with antibiotics and one group without. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| 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: 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: 2005-004457-10 | Sponsor Protocol Number: PS0104 | Start Date*: 2006-01-16 | |||||||||||
| Sponsor Name:Laboratoires Expanscience | |||||||||||||
| Full Title: Clinical and biological activity of Piascledine® 300 in patients with chronic periodontitis | |||||||||||||
| Medical condition: CHRONIC PERIODONTITIS | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-005305-31 | Sponsor Protocol Number: 2013v01 | Start Date*: 2014-03-24 |
| Sponsor Name:Folktandvården Östergötland | ||
| Full Title: Ice as topical anaesthesia before injection in the oral mucosa –a randomized unblinded cross-over study in adolescents. Comparison between ice and lidokain gel 5%. | ||
| Medical condition: The patients should be < 20 years and reffered by an orthodontist with two contra lateral premolars in the upper jaw that has to be extracted. They should not have any diseases or medications that,... | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-000741-39 | Sponsor Protocol Number: 6996 | Start Date*: 2019-11-07 |
| Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||
| Full Title: EFFECT OF AZITHROMYCIN ON THE PROPORTION OF FAILURES OF SEVERE PERIODONTITIS NON-SURGICAL TREATMENTS : A RANDOMIZED, DOUBLE-BLIND VERSUS PLACEBO STUDY | ||
| Medical condition: Periodontology | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| 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: 2014-002625-35 | Sponsor Protocol Number: PERIOC_CTP001 | Start Date*: 2015-01-26 |
| Sponsor Name:PerioC Ltd | ||
| Full Title: The effect of locally delivered ciclosporin as an adjunct to healing after treatment of periodontal pockets | ||
| Medical condition: Moderate to severe chronic periodontitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| 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: 2005-004392-38 | Sponsor Protocol Number: R050187 | Start Date*: 2006-01-12 |
| Sponsor Name:NHS Greater Glasgow/Glasgow University | ||
| Full Title: The feasibility of using Bone Morphogenetic Protein (rhBMP-7) for reconstruction of alveolar cleft | ||
| Medical condition: Autogenous bone graft harvested from the iliac crest is utilised as a gold standard for alveolar reconstruction. However, the harvesting of the bone graft is associated with morbidity which could ... | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-020538-24 | Sponsor Protocol Number: GASAS-1002X | Start Date*: 2011-02-16 |
| Sponsor Name:GABA International AG | ||
| Full Title: White spot lesion development in post-orthodontic patients following weekly application of a 1.25% fluoride gel compared to placebo over 6 months | ||
| Medical condition: To monitor the white spot lesion development and dental status under weekly applied 1.25% fluoride gel compared to placebo in patients after orthodontic treatment with multibracket appliances | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-004606-97 | Sponsor Protocol Number: PMR-EC-1209 | Start Date*: 2007-02-22 | |||||||||||
| Sponsor Name:Astellas Pharma GmbH | |||||||||||||
| Full Title: A MULTICENTER, SINGLE-ARM, OPEN, CONVERSION STUDY FROM A CYCLOSPORINE (CyA) BASED IMMUNOSUPPRESSIVE REGIMEN TO A TACROLIMUS MODFIED RELEASE, FK506E (MR4), BASED IMMUNOSUPPRESSIVE REGIMEN IN KIDNEY ... | |||||||||||||
| Medical condition: Stable, adult kidney transplant recipients (at least 12 months post transplant) who are currently treated with cyclosporine and who meet the Inclusion and Exclusion Criteria will be enrolled. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) BE (Completed) DE (Completed) ES (Completed) CZ (Completed) HU (Completed) FI (Completed) SE (Completed) DK (Completed) AT (Completed) PT (Prematurely Ended) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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