DRKS00011067
Completed
Phase 4
Determination of the Antibacterial Effect of Biodentine in vivo - Identification of Polybacterial 16S rRNA Genes in Caries Samples by T-RFLP and Direct Sequencing
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- K02
- Sponsor
- Septodont
- Enrollment
- 10
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Primary carious dentine lesions at 2 (or more) molars or premolars which are not in contact (e.g. in different sextants), indication to perform a stepwise caries therapy irrespective of the study
- •\-clinical Picture: according to the International Caries Detection and Assessment System (ICDAS) 4, 5 or 6
- •\-complete isolation by rubberdam is possible
- •\-radiographic extension up to the inner half of the dentine (R4\-lesions)
- •\-no clinical symptoms of the study teeth
- •\-positive sensitivity of the study teeth
- •in cases of carious lesion(s) or insufficient restoration margins in proximity of one of the study cavities: clinically acceptable restoration before trial conduction starts
- •signed informed consent
Exclusion Criteria
- •cases of known intolerance of dental materials (or one of their ingrediences) applied in the study course
- •reasons which make it unlikely to be able to determine the outcome or probable consequences of the study (e.g. alcoholism, mental disability)
- •pregnancy, breastfeeding
- •evidence that keeping treatment appointments will not be able
Outcomes
Primary Outcomes
Not specified
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