UnknownNot Applicable

Clinical Evaluation of Bulk-fill Alkasite Restoration Versus Resin Modified Glass Ionomer in Adult With Class V Carious

28 participantsStarted 2021-11-01

Plain-language summary

Cention N will have the same clinical performance as resin-modified glass ionomer in cervical carious lesions. Evaluation of restorations will be done at baseline, six months, and one year according (USPHS) criteria.

Who can participate

Age range18 Years – 50 Years

SexALL

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

Inclusion criteria: * Patients with High caries risk. * Patients with poor oral hygiene. * Patients with untreated cervical caries lesion. * patient aging ≥18 years. * Absence of tooth mobility * Absence of abnormal occlusion. * Patients with good likelihood of recall availability. Exclusion criteria: * Patients with cervical caries lesions need crown restoration. * Non-vital teeth. * Evidence of parafunctional habits. * Teeth supporting removable prosthesis. * Periapical Abscess or Fistula. * Patients with systemic disease. * Patients with xerostomia. * Participants with a history of allergy to any component of restorations will be used in the study.

What they're measuring

(Marginal adaptation)

Timeframe: 12 months

Trial details

NCT IDNCT04716517

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-11-01

View on ClinicalTrials.gov More Cervical Lesion trials