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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04671134
Other study ID # 581/3287
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2017
Est. completion date June 1, 2019

Study information

Verified date December 2020
Source Al-Azhar University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to evaluate the effect of Biomimetic remineralizing agent and resin modified glass ionomer varnish on color shade and state of white spot lesions immediately, after 3 months, and after 6 months. (An in vivo study).


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date June 1, 2019
Est. primary completion date December 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: 1. Patients included in this clinical trial were less than 30 years old. 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: 1. Patients with any systemic disease that may affect normal healing. 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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Biomimetic remineralizing agent
Self-assempling peptide
Resin Modified Glass Ionomer Varnish
Resin Modified Glass Ionomer Varnish

Locations

Country Name City State
Egypt Al-Azhar University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Al-Azhar University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary state of lesions Digital scores 6 months.
Secondary shade of lesions Digital scores 6 months
See also
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