Trials / Completed
CompletedNCT06166849
Clinical Evaluation of an Experimental Remineralization Product
Clinical Study of Tooth Enamel Remineralization Using DoReMin Product
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 43 (actual)
- Sponsor
- Ivoclar Vivadent AG · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The study is designed as a split-mouth randomised controlled study. This means within the mouth of one patient one tooth with an initial lesion is treated and coated with the Experimental Remineralization product whereas another comparable tooth with an initial lesion is left untreated. Patients are included upon meeting the inclusion criteria as defined for this clinical trial. In the test group, a remineralization of the incipient carious lesion is expected. The patients are recalled after 1 day (optional), 4 weeks, 4 months and finally after 1 year to evaluate the untreated and treated lesion.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Experimental Fluoride Application | The two-step system, consisting of Component A and Component B, will be applied once on the white spot lesions |
Timeline
- Start date
- 2023-03-28
- Primary completion
- 2024-05-31
- Completion
- 2025-03-11
- First posted
- 2023-12-12
- Last updated
- 2026-03-27
- Results posted
- 2026-03-27
Locations
1 site across 1 country: Romania
Source: ClinicalTrials.gov record NCT06166849. Inclusion in this directory is not an endorsement.