- Trials with a EudraCT protocol (18)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
18 result(s) found for: Dental caries.
Displaying page 1 of 1.
EudraCT Number: 2009-010725-39 | Sponsor Protocol Number: 56493 | Start Date*: 2009-07-23 | |||||||||||
Sponsor Name:The University of Manchester [...] | |||||||||||||
Full Title: A randomised controlled trial to measure the effects and costs of a dental caries prevention regime for young children attending primary care dental services | |||||||||||||
Medical condition: Dental Caries | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002402-13 | Sponsor Protocol Number: R04684 | Start Date*: 2018-02-02 | |||||||||||
Sponsor Name:Manchester University NHS Foundation Trust | |||||||||||||
Full Title: A Randomised controlled trial to Evaluate the effectiveness and cost benefit of prescribing high dose FLuoride toothpaste in preventing and treating dEntal Caries in high-risk older adulTs (REFLECT... | |||||||||||||
Medical condition: Dental caries in high-risk older adults | |||||||||||||
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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: 2010-023476-23 | Sponsor Protocol Number: SPON766-09 | Start Date*: 2011-03-17 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: Seal or Varnish? A Randomised Trial To Determine The Relative Cost And Effectiveness Of Pit And Fissure Sealants And Fluoride Varnish In Preventing Dental Decay | |||||||||||||
Medical condition: Dental Caries | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002287-26 | Sponsor Protocol Number: GN12CO201 | Start Date*: 2012-10-24 | |||||||||||
Sponsor Name:Greater Glasgow and Clyde NHS Board [...] | |||||||||||||
Full Title: Comparison of the caries-protective effect of fluoride varnish (Duraphat®) with treatment as usual in nursery school attenders receiving preventive oral health support through the Childsmile Progra... | |||||||||||||
Medical condition: Childhood dental caries | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005742-37 | Sponsor Protocol Number: 06/AN/02 | Start Date*: 2007-01-26 | |||||||||||
Sponsor Name:NHS Glasgow and Clyde / University of Glasgow | |||||||||||||
Full Title: Randomised clinical trial of the effects of total intravenous anaesthesia (TIVA: propofol) versus volatile anaesthesia (sevoflurane-N20 induction and isoflurane-N20 maintenance) on children’s post... | |||||||||||||
Medical condition: Dental caries | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006537-14 | Sponsor Protocol Number: 2-geltest | Start Date*: 2008-05-05 |
Sponsor Name:Sven-Åke Lundin | ||
Full Title: 2-geltest: Comparison of plaque-inhibiting efect of toothbrushing with Sodium Fluoride el 0,2 % and Sodium Fluoride.Chlorhexidine Gel 0,2 % + 0,2 % respectively, in treatment of initial and manifes... | ||
Medical condition: Children aged 1-3 yearsr with initial and/or manifest caries on buccal surfaces of their upper incisors | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006104-11 | Sponsor Protocol Number: CHX2007-01 | Start Date*: 2008-12-23 |
Sponsor Name:CHX Technologies Europe Ltd. | ||
Full Title: Phase IV Open-label Pharmaco-economic and Practice Management Study of a New Preventive Treatment for Adult Caries in the U.K. and Germany | ||
Medical condition: Adult dental caries | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) | ||
Trial results: View results |
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: 2005-003845-15 | Sponsor Protocol Number: PHI/03/C1/017 | Start Date*: 2005-12-13 |
Sponsor Name:University of Manchester | ||
Full Title: A cluster randomised control trial to measure the benefit of fluoride varnish in preventing dental decay when applied to the permanent teeth of children for three years in the school setting | ||
Medical condition: Dental caries in first permanent molars | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-005300-29 | Sponsor Protocol Number: SDF1 | Start Date*: 2016-06-06 |
Sponsor Name:Malmö University, Faculty of Odontology | ||
Full Title: Prevention and treatment of initial rotcaries among elderly in Skåne. | ||
Medical condition: Dental caries | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004711-23 | Sponsor Protocol Number: DT11/9936 | Start Date*: 2013-05-22 |
Sponsor Name:Leeds Dental Institute | ||
Full Title: Comparative studies of the anaesthetic efficacy of 4% Articaine used as mandibular infiltration versus 2% Lidocaine used as inferior dental nerve block, in extraction and pulpotomy of mandibular pr... | ||
Medical condition: Dental caries in primary molars | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: GB (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: 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: 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: 2017-003240-20 | Sponsor Protocol Number: 16-058 | Start Date*: 2017-10-12 |
Sponsor Name:RWTH Aachen, represented by the rector, himself represented by the dean of the Medical Faculty | ||
Full Title: Velphoro and impact on the oral cavity and gut microbiome | ||
Medical condition: Hyperphosphatemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-001468-21 | Sponsor Protocol Number: KIIOIW001 | Start Date*: 2006-08-24 |
Sponsor Name:Karolinska Institutet | ||
Full Title: Sympthomatic and prophylactic treatment of drug induced oral dryness in elderly patients with high drug consumption. | ||
Medical condition: Oral dryness is a common problem with serious consquences, especially among elderly individuals. The most common reason for oral dryness is drug consumption. Research has shown that an individual w... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
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 |
EudraCT Number: 2018-001489-41 | Sponsor Protocol Number: P00003466 | Start Date*: 2018-07-02 | |||||||||||
Sponsor Name:Karolinska Universitetssjukhuset | |||||||||||||
Full Title: Radiation- and alkylator-free hematopoietic cell transplantation for bone marrow failure due to dyskeratosis congenita / telomere disease | |||||||||||||
Medical condition: Dyskeratosis congenita / telomere disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
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