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To evaluate the clinical and radiographic success of using Casein Phosphopeptide Amorphous Calcium Phosphate (CPP-ACP) under glass ionomer restorations in atraumatic restorative treatment as a biomimetic approach in pediatric dentistry.
With the growing popularity of ART in the field of pediatric dentistry, a great deal of research has been done in recent years. Researchers are keen to explore the rich possibilities and variations of ART technique that can help doctors practice better and do more for their patients. Alternatives include detours to regenerative dentistry, which is becoming more and more popular these days.
CPP ACP is still of great interest in the region due to its remineralizing action. However, to our knowledge, clinical and radiological success involving tissue regeneration by CPP-ACP is understudied. Furthermore, the studies conducted justify the need for further research on the use of CPP-ACP as an indirect material under glass ionomers in ART. Therefore, this study aims to conclude whether CPP ACP has added value in regenerating, reducing pain, and improving repair retention in caries-affected dentin lesions.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| MI varnish (CPP ACP) under glass ionomer in ART group | Experimental | Application of a thin layer of casein phosphopeptide amorphous calcium phosphate ( CPP ACP ) varnish as indirect pulp capping material under glass-ionomer (Riva Light cure GC company ) in Atraumatic restorative technique. |
|
| Conventional ART | No Intervention | Placement of glass-ionomer restoration ( Riva Light Cure ) only in Atraumatic restorative technique. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| MI varnish | Device | delivers a powerful dose of fluoride, with the added booster effect of the calcium and phosphate ions through its patented Recaldentâ„¢ technology. High initial fluoride release. Minimizes tooth sensitivity and strengthens enamel. Neutral pH of 6,6 enhances enamel and dentin acid resistance and inhibits demineralization |
| Measure | Description | Time Frame |
|---|---|---|
| Post-operative pain | Verbal question to the patient form score 0-5 where o is no pain and maximum pain indicates 5 | 12 months |
| Marginal integrity | Visual and clinical examination (by probe and mirror or any change in color or breakage of restoration, recurrent caries as direct observation) from score 0-5 where 0 gap free marginal interface, 1 indicates mircoleakage occur in 1 surface, 2 in 2 surfaces, 3 in 3 surfaces, 4 in 4 surfaces, 5 loss of whole restoration. | 12 months |
| Measure | Description | Time Frame |
|---|---|---|
| Absence of furcation or periapical radiolucency | Intra oral periapical Xray | 12 months |
| Absence of any internal or external root resorption | Intra oral periapical Xray |
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Clinical Criteria:
Children aged 4-7 years. Apparently healthy children. Children with mild to moderate occlusal carious lesions in the mandibular second primary molar indicated for indirect pulp capping.
No history of spontaneous pain, pathologic mobility, draining sinus tract, redness or swelling of vestibule.
Normal gingival and periodontal condition, with no sensitivity to vestibular palpation, and no pain on percussion test.
Radiographic criteria:
Exclusion Criteria:
Primary molars with more than half of the root resorbed or with periapical pathology as evident radiographically Mobile or ankylosed molars with no permanent successors
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| mai sherif, BDS | Contact | 01117777182 | mai.sherif@dentistry.cu.edu.eg | |
| hany sabr, PHd | Contact | 01225519667 | Hany.sabr@dentistry.cu.edu.eg |
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| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 19089081 | Result | Bresciani E. Clinical trials with Atraumatic Restorative Treatment (ART) in deciduos and permanent teeth. J Appl Oral Sci. 2006;14 Suppl:14-9. doi: 10.1590/s1678-77572006000700004. |
| Label | URL |
|---|---|
| Alexandria university | View source |
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Access to final data will be allowed to the operator (principal investigator) and the main and co-supervisors of the study, who aren't involved in assessing the outcome. All data sets will be password protected. To ensure confidentiality, data dispersed to project team members will be blinded to any identifying participant information.
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| 12 months |