Clinical evaluation of a flowable resin composite in non-carious Class V lesions

two-year results.

Edgar W. Turner, Larry W. Shook, Judith Ross, Waldemar deRijk, Betty C. Eason

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

This in vivo study evaluated the clinical performance and appearance of a flowable resin composite and a hybrid resin composite over two years. Twenty-eight (28) pairs of restorations of a flowable resin composite and a conventional hybrid resin composite were placed in non-carious, asymptomatic facial Class V lesions. The restorations were evaluated at baseline, six, twelve, eighteen and twenty-four (6, 12, 18 and 24) months, using modified Ryge/USPHS criteria. No significant difference (p < 0.05) was observed in the performance or appearance of both materials.

Original languageEnglish (US)
JournalThe Journal of the Tennessee Dental Association
Volume88
Issue number2
StatePublished - Mar 2008

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Composite Resins
United States Public Health Service
flowable hybrid composite
Clinical Studies

All Science Journal Classification (ASJC) codes

  • Medicine(all)

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Clinical evaluation of a flowable resin composite in non-carious Class V lesions : two-year results. / Turner, Edgar W.; Shook, Larry W.; Ross, Judith; deRijk, Waldemar; Eason, Betty C.

In: The Journal of the Tennessee Dental Association, Vol. 88, No. 2, 03.2008.

Research output: Contribution to journalArticle

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