UnknownNot Applicable

Assessment of Bioactive Bulk Fill Composite Versus High Viscosity Glass Ionomer Restorations for Carious Lesions

28 participantsStarted 2022-07-01

Plain-language summary

This trial will be conducted to compare the clinical performance between a new bioactive resin composite material and high viscosity glass ionomer for restoring occlusal carious lesions of posterior teeth in patients scheduled for head and neck radiotherapy.

Who can participate

Age range18 Years – 80 Years

SexALL

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Inclusion criteria

✓. Patients Scheduled for head and neck radiotherapy.
✓. age: ≥18 years.
✓. Patients with good likelihood of recall availability.
✓. Permanent premolars or molars.
✓. Primary occlusal carious lesions.
✓. Vital with positive reaction to cold thermal stimulus.
✓. Well-formed and fully-erupted.

Exclusion criteria

✕. Participants with late stage head and neck cancer
✕. Concomitant participation in another research study.
✕. Inability to comply with study procedures
✕. past experience with allergic reactions against any components of the used materials Teeth with clinical symptoms of pulpitis such as spontaneous pain or sensitivity to pressure.

What they're measuring

Secondary caries

Timeframe: one year follow up

Trial details

NCT IDNCT05332041

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-07-01

View on ClinicalTrials.gov More Secondary Dental Caries trials