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Shade Matching Potential of Universal Shade Resin Composite Materials Compared to Multi Shade Resin Composite in Restoration of Carious Cervical Lesions in Anterior Teeth

Shade Matching Potential of Universal Shade Resin Composite Materials Compared to Multi Shade Resin Composite in Restoration of Carious Cervical Lesions in Anterior Teeth ( Randomized Clinical Trial ) - 1 Year Follow up

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05465850
Enrollment
60
Registered
2022-07-20
Start date
2022-08-31
Completion date
2023-08-31
Last updated
2022-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Class V Dental Caries

Brief summary

The aim of the study is to clinically evaluate the shade matching and clinical performance of the Universal shade composites Omnichroma and GC Essentia versus the multi shade composite Filtek Z350XT in restoring cervical lesions of anterior teeth.

Interventions

DIAGNOSTIC_TESTModified USPHS criteria

It assess the restorations with visual inspection using a mirror and explorer. It includes Marginal integrity, shade matching, retention, marginal discoloration, gingival inflammation, and recurrent caries.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
25 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Class V carious lesions in anterior teeth * Vital upper or lower anterior teeth with no signs of irreversible pulpitis and necrosis. * Presence of favorable occlusion and teeth are in normal contact with the adjacent teeth

Exclusion criteria

* Deep carious defects ( Close to pulp, less than 1 mm distance) * Periapical pathology or signs of pulpal pathology * Endodontically treated teeth * Tooth hypersensitivity * Possible prosthodontic restoration of teeth * Heavy occlusion and occlusal contacts or history of bruxism * Severe periodontal affection * Lesions in premolars and molars * Posterior teeth

Design outcomes

Primary

MeasureTime frameDescription
Clinical performance (USPHS criteria)baseline: 1 weekUSPHS criteria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026