Remineralization Potential of Bioactive Varnish
ConditionWhite Spot Lesion
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age16-35
SponsorFuture University in Egypt
About this trial
This randomized controlled trial is held to investigate the effectiveness of two remineralizing agents surface pre-reacted glass-ionomer (S-PRG) filler and fluoride in management of white spot lesions.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients within 16-35 years of age.
Each patient has 4 or more WSLs
Mild and moderate WSLs.
Good oral hygiene and willing patients who can attend study visits.
Disqualifiers
Active carious lesions.
Labial surface restorations.
Intrinsic and extrinsic stains.
Patients who have a significant medical history or if they are smokers.
Trial design
Design model
Parallel
Treatments tested in this trial
S-PRG barrier coat
Other interventionvarnish containing Surface pre-reacted glass-ionomer technology
Profluorid Varnish
Other interventionFluoride varnish
Treatment groups
60 Participants
are divided into 2 treatment groupsGroup A: S-PRG barrier coatExperimental treatment 1 intervention
Group B: Profluorid VarnishActive comparator 1 intervention
Trial outcomes
Primary outcomes
1
Patients tooth caries lesion state
FDI Criteria (Visual examination of active caries lesion)
Time frame
6 monthsSecondary outcomes
1
Patients' tooth color change
VITA Easy Shade (ΔE)
Time frame
6 monthsLocations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: