Clinical Trial

Clinical Efficacy of Using Bioactive Desensitizer Gel

Completed
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Summary
To evaluate and compare the clinical effectiveness of a Bioactive Desensitizer Gel (which releases calcium and phosphate to form hydroxyapatite) versus a standard 5% Sodium Fluoride (NaF) Varnish in reducing cervical dentin hypersensitivity (CDH) in adult patients over a period of 6 months.
Trial Details
NCT Number NCT07323693
Lead Sponsor Cairo University
Conditions Dentin Desensitizing Agents, Dentin Hypersensitivity, Non-carious Cervical Lesions, Dentin Hypersensitivity
Enrollment 30 participants
Start Date 2024-11-20
Primary Completion 2025-09-20 (estimated)
Study Completion 2025-12-20 (estimated)
Updated on ClinicalTrials.gov 2026-01-07