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OpenTrials
Completed

NCT Number: NCT03415516

Clinical Comparison of Universal Adhesives in Terms of Different Application Modes on the Restoration of NCCLs

The aim of this randomized, controlled, prospective clinical trial is to evaluate the performances of two different universal adhesives and an etch&rinse adhesive in restoration of non-caries cervical lesions. Twenty patients will receive restorations. Lesions will be divided into 7 groups according to adhesive systems and application modes: GSE: Gluma Universal- self etch, GSL: Gluma Universal-selective etching, GER: Gluma Universal-etch&rinse, ASE: All Bond Universal- self etch, ASL: All Bond Universal- selective etching, AER: All Bond Universal- etch&rinse, SB (Control): Single Bond2+etch&rinse. Restorations (nano-hybrid composite) will be scored with regard to retention, marginal discoloration, marginal adaptation, recurrent caries and post operative sensitivity using modified USPHS criteria after 48 months. Two examiners who is not involved in the placement of restorations will conduct the evaluations. Descriptive statistics will be performed using Chi-square tests.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Inclusion criteria

will be as follows:

  • being 18 years or older,
  • having no medical or behavioral problems preventing then from attending review visits,
  • having at least 7 tooth with NCCLs (d) having antagonist teeth.

Exclusion criteria

Exlusion criteria will be:

  • poor gingival health,
  • uncontrolled, rampant caries,
  • bruxism,
  • removable partial dentures,
  • xerostomia.

Treatment and study plan

Gluma Universal

Device

Adhesive systems

All Bond Universal

Device

Adhesive systems

Single Bond2

Drug

Adhesive systems

Primary outcomes

  1. Clinical performances of different adhesives

    Time frame: Two years

    Two year examinations according to USPHS criteria

Sponsors and collaborators

Lead sponsor

Hacettepe University

Other

Registry information

Important dates

Study start
2015
Primary completion
2015
Study completion
2018
First posted
Jan 30, 2018
Registry last updated
Sep 14, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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