Trials / Completed
CompletedNCT07323693
Clinical Efficacy of Using Bioactive Desensitizer Gel
Clinical Efficacy of Using Bioactive Desensitizer Gel Versus Sodium Fluoride Varnish on Cervical Dentin Hypersensitivity in Adult Patients: A 6m Randomized Clinical Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 30 (actual)
- Sponsor
- Cairo University · Academic / Other
- Sex
- All
- Age
- 18 Years – 30 Years
- Healthy volunteers
- Accepted
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.
Conditions
- Dentin Desensitizing Agents
- Dentin Hypersensitivity, Non-carious Cervical Lesions
- Dentin Hypersensitivity
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Treatment | A micro-brush applicator was saturated with the material (Predicta Bioactive Desensitizer Gel) and massaged it into the tooth for 30-40 secs. Using a rubbing motion was used to liquefy the gel and allow it to penetrate the surface |
| PROCEDURE | Treatment | the sodium fluoride (Proshield) varnish, was painted with a disposable micro-brush on the sensitive surface as per the instructions for 60 seconds from the manufacturer. |
Timeline
- Start date
- 2024-11-20
- Primary completion
- 2025-09-20
- Completion
- 2025-12-20
- First posted
- 2026-01-07
- Last updated
- 2026-01-07
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT07323693. Inclusion in this directory is not an endorsement.