Evaluation of State and Shade of White Spot Lesions After Using Different Remineralizing Agents (An in Vivo Study)
NCT ID: NCT04671134
Last Updated: 2020-12-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
20 participants
INTERVENTIONAL
2017-06-01
2019-06-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Biomimetic remineralizing agent
Biomimetic remineralizing agent
Self-assempling peptide
Resin Modified Glass Ionomer Varnish
Resin Modified Glass Ionomer Varnish
Resin modified glass ionomer varnish
Biomimetic remineralizing agent
Self-assempling peptide
Resin Modified Glass Ionomer Varnish
Resin Modified Glass Ionomer Varnish
Interventions
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Biomimetic remineralizing agent
Self-assempling peptide
Resin Modified Glass Ionomer Varnish
Resin Modified Glass Ionomer Varnish
Eligibility Criteria
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Inclusion Criteria
2. Patients with good general health.
3. Patients who will agree to the consent and will commit to follow-up period.
4. Fully erupted anterior teeth with no cavitated lesions.
Exclusion Criteria
2. Patient with bad oral hygiene.
3. Tetracycline or florosis staining.
4. Patients who could/would not participate in all times of follow-up.
5. Untreated periodontal disease was not allowed.
6. Active caries or defective Restorations in 6 anterior teeth.
7. Bleaching history
8. Patients participating in more than 1 dental study.
9. Patient received fluoride varnish before.
18 Years
30 Years
ALL
Yes
Sponsors
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Al-Azhar University
OTHER
Responsible Party
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Hany Helmy Elsayed Mohammed
Principle Investigator
Locations
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Al-Azhar University
Cairo, , Egypt
Countries
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Other Identifiers
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581/3287
Identifier Type: -
Identifier Source: org_study_id