10 Years Evaluation of Composite Restoration

B

BNM Clinic and Research

Status

Completed

Conditions

Dental Restoration, Permanent

Treatments

Device: Astralis 10 RM
Device: Astralis 10 HPM

Study type

Interventional

Funder types

Other

Identifiers

NCT02764450
TEX-10y-2016

Details and patient eligibility

About

This randomised, split-mouth clinical study evaluated the marginal quality of direct Class I and Class II restorations made of microhybrid composite and applied using two polymerisation protocols,

Enrollment

50 patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • subjects at least 18 years old,
  • require restorations due to primary caries in contralateral quadrants with opposing and adjacent tooth contact,
  • having no restoration in the antagonist,

Exclusion Criteria

  • allergic to resin-based materials,
  • pregnant or nursing,
  • periodontal disease

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

50 participants in 2 patient groups

Astralis 10 HPM
Experimental group
Description:
Polymerization High-power mode: 1300 mW/cm2 for 10 s
Treatment:
Device: Astralis 10 RM
Astralis 10 RM
Experimental group
Description:
Polymerisation regular mode: 650 mW/cm2 for 20
Treatment:
Device: Astralis 10 HPM

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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