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36-Month Clinical Evaluation of a Universal Adhesive

H

Hacettepe University

Status

Completed

Conditions

Non-Carious Cervical Lesions

Treatments

Device: Scotchbond Universal Adhesive (3M ESPE)

Study type

Interventional

Funder types

Other

Identifiers

NCT03932929
KA-17088

Details and patient eligibility

About

The aim of this clinical trial was to evaluate and compare the performance of a universal adhesive with different adhesive strategies in the restoration of non-carious cervical lesions (NCCLs) over a 36-month period.

Full description

One hundred sixty-five NCCLs in 35 patients (13 female, 22 male) with at least 3 lesions were included in this study. Three groups were formed according to adhesive strategies used (n=55): selective-etch mode; etch-and-rinse mode (ER); or self-etch (SE) mode of a universal adhesive, Single Bond Universal. The same nanofilled resin composite, Filtek Ultimate was used for all restorations by a single operator. The restorations were evaluated by two calibrated examiners at baseline and at 6-, 12-, 18-, 24- and 36- months in accordance with the modified USPHS criteria. The Chi-square test was used for intergroup, the Cochran Q test was used for intragroup comparison.

Enrollment

35 patients

Sex

All

Ages

18 to 81 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • over 18 years old
  • good oral hygiene
  • available for recall
  • at least 20 teeth under occlusion
  • the presence of at least three non-carious cervical lesions

Exclusion criteria

  • poor oral hygiene
  • bruxism habits
  • severe or chronic periodontitis
  • If the teeth selected for study, were nonvital, or had any restorations on other surfaces were not included.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

35 participants in 3 patient groups

Scotchbond universal adhesive (etch-and-rinse)
Experimental group
Description:
Acid etch (enamel\&dentin)+adhesive agent Intervention: Device: Adhesive agent
Treatment:
Device: Scotchbond Universal Adhesive (3M ESPE)
Scotchbond universal adhesive (selective-etch)
Experimental group
Description:
Acid etch (only enamel)+adhesive agent Intervention: Device: Adhesive agent
Treatment:
Device: Scotchbond Universal Adhesive (3M ESPE)
Scotchbond universal adhesive (self-etch)
Experimental group
Description:
Adhesive agent Intervention: Device: Adhesive agent
Treatment:
Device: Scotchbond Universal Adhesive (3M ESPE)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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