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

R

Recep Tayyip Erdogan University Training and Research Hospital

Status

Withdrawn

Conditions

Noncarious Cervical Lesions

Treatments

Other: EQUIA Forte Fil
Other: NexComp Flow
Other: Clearfil Majesty Esthetic
Other: 3M Espe Bulk-fill

Study type

Interventional

Funder types

Other

Identifiers

NCT04261140
2019/19

Details and patient eligibility

About

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

Full 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.

Sex

All

Ages

20 to 60 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

0 participants in 4 patient groups

High-viscosity glass ionomer
Experimental group
Treatment:
Other: EQUIA Forte Fil
flowable composite
Experimental group
Treatment:
Other: NexComp Flow
bulkfill composite
Experimental group
Treatment:
Other: 3M Espe Bulk-fill
nanohybrid composite
Experimental group
Treatment:
Other: Clearfil Majesty Esthetic

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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