This study is currently not recruiting participants.

CLINICAL EVALUATION OF A UNIVERSAL ADHESIVE IN NONCARIOUS CERVICAL LESIONS

  • STATUS
    Not Recruiting
Updated on 19 February 2024

Summary

The purpose of this prospective clinical trial will be to evaluate the efficacy of a newly formulated ?universal? dental adhesive formulation in adult noncarious cervical lesions using self-etch and selective etch approaches; the aim is to determine whether or not selective etching provides significantly improved retention and/or better resistance to enamel margin discoloration in comparison to self-etching over a 24 month period.

Description

The purpose of this prospective clinical trial will be to evaluate the efficacy of a newly formulated ?universal? dental adhesive formulation in adult noncarious cervical lesions using self-etch and selective etch approaches; the aim is to determine whether or not selective etching provides significantly improved retention and/or better resistance to enamel margin discoloration in comparison to self-etching over a 24 month period.

Details
Age 100years or below
Clinical Study IdentifierTX4542
Last Modified on19 February 2024

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