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One-year Clinical Evaluation of Bulk-fill Versus Conventional Incremental Posterior Restoration by FDI Criteria

Cairo University (CU) logo

Cairo University (CU)

Status

Enrolling

Conditions

Post Dental Restoration

Treatments

Other: bulk fill composite
Other: Nano resin composite (K Z350 xt)

Study type

Interventional

Funder types

Other

Identifiers

NCT02891967
CEBD-CU-08-184

Details and patient eligibility

About

restoring posterior teeth by bulk fll and nanofill composite and clinical evaluation of performance and durability of both restorations during one year follow up

Full description

The treated cavities will be divided into 2 groups, cavities will be incrementally layered with resin composite and each increment will be cured as directed by the manufacturer with the light curing unit (XL 3000; 3M/eSPe), with an energy higher than 450 mW/cm² (±50 mw/cm²) and other group of cavities will be restored by bulk fill composite (3M ESPE) as one increment then will be cured as directed by the manufacturer with the light curing unit.

Articulation will be checked carefully with an articulating paper and occlusal adjustments will be performed using flame shaped carbide and diamond finishing burs (DENTSPLY) using water spray, restorations will be finished occlusally with finishing burs and finally polished with aluminium oxide polishing paste and a rubber cup (DENTSPLY).

Enrollment

69 estimated patients

Sex

All

Ages

18 to 38 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Good oral hygiene.Patients must show no signs of orofacial pain. The presence of molar teeth requiring composite restorations for the treatment of primary carious lesions

Exclusion criteria

  • Teeth with abnormal periapical anatomy or caries that will be likely to result in very deep restorations. Teeth with old restorations or severely destructed dental crowns.Tempro-mandibular joint problems involving symptomatic pain.Pregnancy or breast feeding, acute and chronic systemic diseases, immune-compromised patients

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

69 participants in 2 patient groups

Bulk full composite (3M)
Other group
Description:
bulk fill composite in posterior class one cavities
Treatment:
Other: Nano resin composite (K Z350 xt)
Other: bulk fill composite
Incremental packing composite resin
Other group
Description:
Nano resin composite (K Z350 xt) restoration in class one cavities
Treatment:
Other: Nano resin composite (K Z350 xt)
Other: bulk fill composite

Trial contacts and locations

1

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Central trial contact

Mina GA Awad, Phd; Mary ST Tadros, Phd

Data sourced from clinicaltrials.gov

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