- Trials with a EudraCT protocol (41)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
41 result(s) found for: Oral hygiene.
Displaying page 1 of 3.
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: 2004-002366-38 | Sponsor Protocol Number: P305 R-EF02 | Start Date*: 2004-11-16 |
Sponsor Name:GABA GmbH | ||
Full Title: Fluoride uptake and remineralisation of incipient carious lesions following the application of fluoride fluids with different fluoride concentrations | ||
Medical condition: caries lesions | ||
Disease: | ||
Population Age: Adults | 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: 2008-008594-58 | Sponsor Protocol Number: GASAS-0809X | Start Date*: 2009-07-24 |
Sponsor Name:GABA International AG | ||
Full Title: In situ mineral change and fluoride retention of sound and demineralized enamel in high cariogenic milieus following the single application of a 1.25%- fluoride or a placebo gel. | ||
Medical condition: Remineralization, fluoride uptake, and lesion depth of sound and demineralized, plaque-covered enamel after the application of elmex gel will be tested in situ in comparison to a placebo gel. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (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: 2017-001068-39 | Sponsor Protocol Number: ECPAF11/16 | Start Date*: 2018-07-24 |
Sponsor Name:OMEQUI | ||
Full Title: Changes in the bone morphology of the post-extraction socket, preserved with platelet-rich fibrin and leukocytes (L-PRF) versus Conventional treatment | ||
Medical condition: Regenerative potential of L-PRF | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000736-25 | Sponsor Protocol Number: IB3M.2019 | Start Date*: 2019-09-05 |
Sponsor Name:Universidad Complutense de Madrid | ||
Full Title: Efficacy of Non-Steroidal Anti-Inflammatory (Ibuprofen) Chronotherapy in Healing After Mandibular Third Molar Surgical Extraction – A Randomized Clinical Trial | ||
Medical condition: The clinical trial will try to understand if the elimination of the ibuprofen dosage in resting phase after surgical third molar extraction not jeopardize the postoperative period . | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004083-62 | Sponsor Protocol Number: steroid3848 | Start Date*: 2019-09-06 |
Sponsor Name:Semmelweis University, Oro-Maxillofacial Surgery and Stomatology | ||
Full Title: Effect of preoperative intramasseteric methylprednisolone injection on the post-operative sequelae of lower third molar surgery: a placebo controlled, randomized, double-blinded study | ||
Medical condition: post-operative swelling, trismus, pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000141-31 | Sponsor Protocol Number: ISRCTN30952488 | Start Date*: 2016-08-30 | |||||||||||
Sponsor Name:London School of Hygiene and Tropical Medicine | |||||||||||||
Full Title: A SERIES OF RANDOMISED CONTROLLED N-of 1 TRIALS IN PATIENTS WHO HAVE DISCONTINUED OR WISH TO DISCONTINUE STATIN USE DUE TO MUSCLE-RELATED SYMPTOMS TO ASSESS IF ATORVASTATIN TREATMENT CAUSES MORE MU... | |||||||||||||
Medical condition: myalgia | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003172-39 | Sponsor Protocol Number: Mica1/2012 | Start Date*: 2013-05-23 |
Sponsor Name:Medizinische Universität Innsbruck, Abteilung für Hygiene und Medizinische Mikrobiologie | ||
Full Title: Micafungin-Deescaltion study: Evalutating the rate of breakthrough infections of micafungin followed by fluconazole versus fluconazole (or other azoles) in febrile patients | ||
Medical condition: All patients who are suspicious of suffering from invasive fungal infections are included. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002193-40 | Sponsor Protocol Number: DT-001-R-004 | Start Date*: 2018-04-04 | |||||||||||
Sponsor Name:Afyx Therapeutics A/S | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel Group Clinical Study to Assess the Safety and Efficacy of Three Doses of Clobetasol Propionate when Administered Intra-orally Twice Daily in... | |||||||||||||
Medical condition: Oral Lichen Planus (OLP). OLP is a common, chronic mucosal disease associated with a cell-mediated immunological dysfunction and characterized by exacerbations of inflammation, which can lead to ul... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) DK (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005511-32 | Sponsor Protocol Number: XEOLAS | Start Date*: 2022-09-12 |
Sponsor Name:Xeolas Pharmaceuticals Ltd. | ||
Full Title: A Randomized Control Trial Phase (IIIa) Unicentric, Placebo Controlled, Double-Blinded Study to confirm the Efficacy and Safety of “Effects of topical Alendronic Acid on alveolar bone remodeling af... | ||
Medical condition: Healthy patients periodontal disease, that qualify for oral surgery of the alveolar bone(ASA I and II) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005854-61 | Sponsor Protocol Number: ABPARO | Start Date*: 2008-02-15 | |||||||||||
Sponsor Name:University Hospital Muenster | |||||||||||||
Full Title: Adjunctive antimicrobial therapy of periodontitis: Long-term effects on disease progression and oral microbiological colonization | |||||||||||||
Medical condition: periodontal disease (moderate to severe) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019513-24 | Sponsor Protocol Number: 10_022 | Start Date*: 2011-03-03 |
Sponsor Name:London School of Hygiene & Tropical Medicine | ||
Full Title: Antibiotics for exacerbations of chronic obstructive pulmonary disease: a pilot randomised trial within the General Practice Research Database | ||
Medical condition: Diagnosed at a GP visit as suffering from acute exacerbation of COPD a. Medical history of COPD b. Increase in dyspnoea AND increase of (non-purulent) sputum volume | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-018399-25 | Sponsor Protocol Number: MuSH_1.2 | Start Date*: 2011-03-17 | |||||||||||||||||||||
Sponsor Name:Medizinische Universität Wien, Univ.Klinik für Zahn-,Mund-u.Kieferheilkunde,Klin.Abt.f.orale Chirurg | |||||||||||||||||||||||
Full Title: A randomized controlled trial: Photodynamic Treatment for the therapy of premalignant mucosal oral lesions. | |||||||||||||||||||||||
Medical condition: Leukoplakia and oral lichen ruber. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000285-38 | Sponsor Protocol Number: APHP190020 | Start Date*: 2019-08-21 |
Sponsor Name:London School of Hygiene and Tropical Medicine | ||
Full Title: Pharmacokinetics of Tranexamic Acid after oral, intramuscular or intravenous administration: a prospective, randomised, cross-over trial in healthy volunteers. | ||
Medical condition: healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
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: 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: 2009-014913-28 | Sponsor Protocol Number: 09_056R | Start Date*: 2011-02-03 |
Sponsor Name:London School of Hygiene & Tropical Medicine | ||
Full Title: RETRO-PRO: The effectiveness of simvastatin compared to atorvastatin: an e-clinical randomised trial within a research database in routine clinical practice - a feasibility study | ||
Medical condition: subjects who in the opinion of the GP investigator would require a statin for primary prevention according to the 2008 NICE guideline on lipid modification: adults over 40 who have a 20% or greater... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-003139-50 | Sponsor Protocol Number: Maxillo1 | Start Date*: Information not available in EudraCT |
Sponsor Name:University of Bergen, Faculty of medicin and dentistry, Dep. of Clinical Dentistry | ||
Full Title: International, multicenter phase II uncontrolled prospective clinical trial: Jaw bone reconstruction using a combination of biomaterial and autologous mesenchymal stem cells prior to dental impla... | ||
Medical condition: Men and women aged 18 years or more requiring jaw bone reconstruction prior to dental implant placement based on clinical and radiological examinations (CBCT Cone beam CT imaging). Areas suitable ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
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