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Comparison of Two Universal Composites in Posterior Teeth

H

Hacettepe University

Status

Completed

Conditions

Dental Caries

Treatments

Other: Charisma
Other: Charisma Classic

Study type

Interventional

Funder types

Other

Identifiers

NCT02888873
2014/03-13(KA-14005)

Details and patient eligibility

About

The aim of this randomized, prospective clinical study was to compare the clinical performance of a universal light-curing, ultra-fine particle hybrid composite with a new version of this product produced by the same manufacturer in Class 1 and Class 2 lesions.

Full description

A total of 80 (13 Class 1 and 67 Class 2) lesions in 40 patients (21 females, 19 males) with ages ranging between 18-38 years (23.15±5.15) were either restored with Charisma or Charisma Classic (Heraeus Kulzer) in combination with an etch and rinse adhesive system (Gluma 2 Bond) under rubber dam isolation by two experienced operators according to the manufacturer's instructions. Two independent examiners, who were blinded to the composites used evaluated the restorations according to the FDI (World Dental Federation) criteria. Bite-wing radiographs and intraoral digital photographs were taken before and after treatment and at 6 months. The statistical analyses were carried out with McNemar, Pearson Chi-square and Cochran Q tests (p<0.05).

Enrollment

40 patients

Sex

All

Ages

18 to 38 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • a need for at least two but not more than four posterior tooth-colored restorations
  • the presence of teeth to be restored in occlusion
  • teeth that were symptomless and vital
  • a normal periodontal status
  • a good likelihood of recall availability.

Exclusion criteria

  • partly erupted teeth
  • absence of adjacent and antagonist teeth
  • poor periodontal status
  • adverse medical history
  • potential behavioral problems.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

40 participants in 2 patient groups

Charisma
Active Comparator group
Description:
applied randomly
Treatment:
Other: Charisma
Charisma classic
Active Comparator group
Description:
applied randomly
Treatment:
Other: Charisma Classic

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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