Caries Clinical Trial
Official title:
Evaluation of the Fluoride Dose Response of a Modified In Situ Caries Model
The purpose of this study is to evaluate the fluoride dose response of different dentifrice fluoride concentrations - 0, 250, 500 and 1100 ppm fluoride of our existing in situ model involving the use of human enamel specimens placed in the buccal flange area of the subjects partial denture with the modified model involving placement of bovine enamel specimens in a denture tooth location.
This will be a double blind, single center, 4-way crossover design study involving 34 adult subjects, between the ages of 18 and 85 years. Two to three days before the start of each treatment period the subjects will have their teeth cleaned to remove all accessible plaque and calculus and will be provided with a non-fluoride dentifrice to use until their next visit. At the beginning of each testing period, two gauze-covered 4 × 4 mm partially demineralized human enamel specimens will be placed in the buccal flange area of the subject's mandibular partial denture. In addition, two gauze-covered 4 mm round partially demineralized bovine enamel specimens will be placed in the buccal surface of two posterior denture teeth of the same side of the partial denture. Once specimens are placed, subjects will wear their partial dentures twenty-four hours a day and use their assigned toothpaste twice daily, as instructed, until their next visit. Specimens will be removed after two weeks and the subjects will undergo a four to five day washout period followed by another cleaning and two to three day lead in period. This process will be repeated until all subjects have used all four test products. Changes in the mineral content of the enamel specimens will be assessed using the SMH and TMR. Enamel fluoride uptake (EFU) will be determined using the microdrill enamel biopsy technique. In addition the net acid resistance (NAR) and the comparative acid resistance (CAR) of the remineralized enamel specimens will be determined. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT05311657 -
Oral Health and Severe COPD
|
||
Not yet recruiting |
NCT06438926 -
Prevalence of Dental Caries in Patients With Dental Crowding
|
||
Completed |
NCT01529606 -
Cold Plasma for Dental Restoration and Caries Prevention
|
N/A | |
Completed |
NCT06072742 -
Effect of Lifestyle on Caries and Apical Periodontitis
|
||
Completed |
NCT04679558 -
Antibacterial Effect of Chlorhexidine Added to the Preventive Protocol in Adolescent Special Needs
|
Early Phase 1 | |
Active, not recruiting |
NCT04933123 -
Clinical Evaluation of a Dental Glass Ceramic in the Indirect Restorative Therapy
|
N/A | |
Withdrawn |
NCT02202304 -
The Effects of Chlorhexidine/Thymol Varnish on Partial Denture Patient
|
Phase 4 | |
Not yet recruiting |
NCT04889196 -
The Efficiency and Gingival Health Status of Hall Versus SDF Techniques in the Management of Carious Primary Molars
|
Phase 3 | |
Active, not recruiting |
NCT04708223 -
Prospective, Split-mouth, Comparative Study to Compare Clinical Outcomes of Two Different Posterior Composite
|
N/A | |
Completed |
NCT06140745 -
Evaluation of Dentifrice Formulations to Remineralize Enamel and Dentine Subsurface Lesions in a Double-Blind In-Situ Clinical Trial
|
N/A | |
Recruiting |
NCT05144711 -
Management of Deep Carious Lesions in Adults
|
N/A | |
Not yet recruiting |
NCT03656432 -
Effect of CPP-ACP With/Without Fl on White Spot Lesion,Salivary pH and fl Release in High Caries Risk Patients
|
Phase 3 | |
Not yet recruiting |
NCT02933463 -
Clinical Effectiveness of Embrace Wetbond and Clinpro as Pits and Fissure Sealants in Young Permanent Molars
|
N/A | |
Completed |
NCT02998814 -
Clinical Follow Up of a Fissure Sealant Placed With Different Adhesive Protocols: 2-Year Randomized Split Mouth Study
|
N/A | |
Completed |
NCT02027597 -
Improving Oral Health With Serious Games
|
N/A | |
Not yet recruiting |
NCT05064566 -
Evaluation of Caries Detection Methods
|
||
Completed |
NCT06010732 -
In Situ Comparison of the Remineralization Potential of Optimized Fluoride Dentifrice With Control Fluoride Dentifrice
|
Phase 3 | |
Recruiting |
NCT05211843 -
Saliva Insulin as Biomarker of Risk Factors for Metabolic Dysregulation and Caries
|
N/A | |
Not yet recruiting |
NCT05070416 -
Lithium Disilicate Crowns Study
|
N/A | |
Completed |
NCT02418520 -
The Effect of Miswak Chewing Sticks on the Oral Helicobacter Pylori Infection
|
N/A |