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Clinical Evaluation of Four Aesthetic Restorations in Non-carious Cervical Lesions

Not Applicable
Withdrawn
Conditions
Noncarious Cervical Lesions
Registration Number
NCT04261140
Lead Sponsor
Recep Tayyip Erdogan University Training and Research Hospital
Brief Summary

To compare the clinical performance of high-viscosity glass ionomer, flowable composite, bulkfill composite and nanohybrid composite restorations in non-carious cervical lesions (NCCLs).

Detailed Description

One hundred fourty NCCLs were randomised into four groups according to a split-mouth design. Clinical evaluations will be performed after 1 week, 3 months, 6 months, using FDI (World Dental Federation) criteria.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • had at least four non-carious symmetrical cervical lesions,
  • had permanent dentition and were older than 20 years old,
  • had cervical margins in dentin
Exclusion Criteria
  • periodontal disease
  • pregnant or breastfeeding
  • being under orthodontic therapy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
evaluation of restoration on cervical lesions6 months

According to FDI criteria (aesthetic, biological and fuctional) score 1, clinically very good; score 2, clinically good; score 3, clinically sufficient; score 4, clinically unsatisfactory; score 5, clinically poor. Scores 1-3 show clinically acceptable restoration, while scores 4 and 5 indicate failure

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Recep Tayyip Erdogan University Dentistry Faculty

🇹🇷

Rize, Turkey

Recep Tayyip Erdogan University Dentistry Faculty
🇹🇷Rize, Turkey

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