aboratory and clinical evaluation of resin composite placed in one increment in posterior teeth restorations

Not Applicable

• Conditions: Dental caries, dentin sensitivity, dental restoration failure, dental restoration wear; E06.780.345.737.125; E06.323.400; C07.793.266

• Registration Number: RBR-5kb5kz
• Lead Sponsor: niversidade Estadual de Ponta Grossa - UEPG

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-02-11
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruitment completed
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Participants must be healthy; be at least sixteen posterior teeth in occlusion; minimum age of 18 years; have at least two caries or defective restorations in need of replacement in posterior teeth (cavities adjacent to the restoration, fractured restorative material or patient choice of aesthetics); the teeth to be restored should be in occlusion with the antagonist and respond positively to pulp vitality test performed with the application of cold (Roeko Endo-Frost, Coltène / Whaledent, Langenau, Germany, the cavities to be restored must have a minimum depth 3 mm (previously verified by bitewing radiography exam and millimeter probe)

Exclusion Criteria

We excluded participants with poor oral hygien; with periodontal disease; endodontic treatment; with extensive prostheses (fixed or removable) or orthodontic treatment; with known allergy to resin-based materials or any other material used in this study; patients with chronic use of anti-inflammatories, analgesics and psychotropic drugs; pregnant or breastfeeding women.

Study & Design

• Study Type: Intervention
• Study Design: Not specified