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Posterior CAD/CAM Cobalt-chromium Alloy Single Crowns: 4-year Prospective Clinical Study

F

Federico II University

Status

Completed

Conditions

Single Tooth Lost

Treatments

Other: Periodontal parameters
Device: Co-Cr single crown

Study type

Interventional

Funder types

Other

Identifiers

NCT02956174
FZ_Co-Cr_2016

Details and patient eligibility

About

Objectives - To evaluate the 4-year clinical outcomes of ceramic veneered Computer Aided Design/Computer Aided Manufacturing (CAD/CAM) Co-Cr single crowns supported by natural teeth in posterior regions.

Material and methods - Eighty-nine patients were provided with 120 ceramic veneered CAD/CAM Co-Cr single crowns replacing either premolars and molars. Specific inclusion criteria were needed and tooth preparations were standardized and performed by 2 expert prosthodontists. CAD/CAM Co-Cr frameworks were fabricated and veneered with ceramics. The restorations were cemented using a eugenol-free zinc oxide luting agent. The patients were recalled after 1, 6, 12, 24, 36 and 48 months. The survival and success of the restorations were evaluated. The technical and esthetic outcomes were examined using the United States Public Health Service criteria. The biologic outcomes were analyzed at abutment and contralateral teeth and descriptive statistics were performed.

Enrollment

89 patients

Sex

All

Ages

21 to 68 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • good general health
  • American Society of Anesthesiologists (ASA) ASA I or ASA II condition; periodontal health
  • Angle class I occlusal relationship
  • minimum of 10 couples of opponent teeth
  • good oral hygiene
  • no evident signs of parafunctions and/or temporomandibular disorders.
  • periodontal health of abutment teeth (absence of tooth mobility, absence of furcation involvement);
  • proper positioning of abutment teeth in the dental arch (tooth axis adequate for a SC)
  • sufficient occlusal-cervical height of the clinical crown of abutment teeth (≥ 4 mm) for the retention of a SC
  • vital or endodontically treated to a clinically sound state abutment teeth;
  • abutment teeth opposing natural teeth.

Exclusion criteria

  • high caries activity
  • presence of periodontal disease on the abutment tooth
  • occlusal-cervical height of the abutment tooth < 4 mm
  • reduced interocclusal distance or supraerupted opposing teeth
  • unfavorable crown-to-root ratio
  • severe were facets, clenching and/or bruxism
  • presence of removable partial dentures (RPDs)
  • pregnancy or lactation
  • alcohol and/or drug addiction

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

89 participants in 2 patient groups

Co-Cr single crown
Experimental group
Description:
Co-Cr single crown
Treatment:
Other: Periodontal parameters
Device: Co-Cr single crown
Contralateral sound tooth
Active Comparator group
Description:
Contralateral sound tooth
Treatment:
Other: Periodontal parameters

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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