Carious Tissue Selective Removal on Permanent Posterior Teeth.

Status Recruiting

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04533113
Study type	Interventional
Source	Universitat Internacional de Catalunya
Contact
Status	Recruiting
Phase	N/A
Start date	February 20, 2019
Completion date	July 2026

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