By InvitationNot Applicable

Clinical Evaluation of Different Bioactive Restorative Materials for Cervical Carious in High Caries Risk Patients

Egypt30 participantsStarted 2024-10-01

Plain-language summary

The aim of the study is to clinically evaluate three different bioactive restorative material in cervical carious lesion in high caries risk patients. Reducing the incidence of recurrent caries is the primary outcome

Who can participate

Age range25 Years – 45 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patient age range from 25-45 year. * High risk caries. * Patients required at least a couple of Class V restorations. * The depth of lesion should be(1.5- 2 mm) . * The patient should have good general health Exclusion Criteria: * Poor oral hygiene. * Sever or chronic periodontal disease or Bruxism. * Severe tooth sensitivity. * Non-vital or fracture or cracked teeth. * Defective restorations, orthodontic treatment or bleaching procedures during the last 6 months. * pregnancy, and/or lactation, and allergy to the main components of the products to be used in the study

What they're measuring

clinical performance (Post operative hyper sensitivity)

Timeframe: 12 months

Trial details

NCT IDNCT06736964

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-04-01

View on ClinicalTrials.gov More Class V Dental Caries trials