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RecruitingNCT04533113

Carious Tissue Selective Removal on Permanent Posterior Teeth.

Carious Tissue Selective Removal on Permanent Posterior Teeth. A Randomized Controlled Clinical Study.

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
111 (estimated)
Sponsor
Juan Gonzalo Olivieri · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

This study is a prospective randomized controlled study of patients who come to the University. The aim is to evaluate the success rate of selective removal of carious tissue in deep lesions of posterior teeth. Three different materials will be used as liners (VitreBond ™Plus, BioDentine™, and Theracal™ LC). Post-operative pain, clinical, and radiographic success will be evaluated at one, two, and five-year follow-up. The null hypothesis is that there will be no statistically significant differences in rates of successful treatment with the three materials used.

Conditions

Interventions

TypeNameDescription
PROCEDURECarious tissue selective removalCarious tissue selective removal in deep carious lesions in posterior teeth, using one of three materials as a liner under the final composite restoration

Timeline

Start date
2019-02-20
Primary completion
2021-07-01
Completion
2026-07-01
First posted
2020-08-31
Last updated
2020-08-31

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT04533113. Inclusion in this directory is not an endorsement.

Carious Tissue Selective Removal on Permanent Posterior Teeth. (NCT04533113) · Clinical Trials Directory