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Evaluate clinically the remineralizing potential of self-assembling peptide ( P11-4) fluoride plus in early enamel carious lesions of permanent anterior teeth.
Full description
Study design This study will be conducted as a randomized controlled clinical trial. Study setting The study will be carried out in the clinic of Pediatric Dentistry Department, Faculty of Dentistry, Tanta University.
Group assignment:
Fifty children will be randomly allocated using simple random table into two groups as follows:
Ethical consideration The purpose of the present study will be explained to both the parents and children and informed consents will be obtained as well as ascents from children .The researcher will be obligated to do dental treatment for every child according to his-her condition as compensation according to the guidelines on human research adopted by the Research Ethics Committee, Faculty of Dentistry, Tanta University.
Materials to be used in the study:
Materials Composition Manufacture Trade names
Fluoride varnish
5% sodium fluoride (22.600ppm) Dentkist-korea Charm varnish R
Self-assembling peptide p11-4 Sodium Fluoride 0.05% Water,Chlorhexidine digluconate,Tromethamine, Trehalose Dihydrate, Oligopeptide-104, HydroxyPropyl MethylCellulose,Citric Acid,Sodium Hydroxide Credentis AG, Windisch, Switzerland CURODONT Repair ™ fluoride plus Polishing paste fluoride free Titanium Oxide Crosstex- Chicago,US Sparkle Free Prophy Paste
Methods
Clinical examination and assessments:
Clinical procedure:
In all groups children will be advised to:
Evaluation:
The remineralizing process of the early enamel carious lesions will be assessed qualitatively using ICDAS II scoring system (table 1) and quantitatively using the laser fluorescence DIAGNOdent measuring at baseline 1, 3, 6 months post-treatment
Enrollment
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Primary purpose
Allocation
Interventional model
Masking
50 participants in 2 patient groups
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Central trial contact
Sara Elgebaly, master
Data sourced from clinicaltrials.gov
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