This study is currently not recruiting participants.

CLINICAL EVALUATION OF A UNIVERSAL ADHESIVE IN NONCARIOUS CERVICAL LESIONS

Not Recruiting
100 years or below
All
Phase N/A

Brief description of study.

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.

Detailed description of study

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.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions:
  • Age: 100 years or below
  • Gender: All
Updated on 04 Dec 2014. Study ID: 1403626552

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