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NCT04671134 Clinical Trial

Evaluation of State and Shade of White Spot Lesions After Using Different Remineralizing Agents (An in Vivo Study)

White Spot Lesion Clinical Trial

Official title:
Evaluation of State and Shade of White Spot Lesions After Using Different Remineralizing Agents (An in Vivo Study)

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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Active, not recruiting NCT04342858 - Prospective Randomized Controlled Trial for Prevention of Demineralization During Fixed Orthodontic Treatment Phase 2
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Completed NCT06200129 - İmportance of Scattered White Spots Detected in the Duodenum and Their Relationship wıth Zonulin N/A
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Not yet recruiting NCT06051981 - White Spot Lesions Treatment in Orthodontic Phase 4
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Completed NCT05775250 - Evaluation of Two Varnishes on the Improvement of White Spot Lesions in Children N/A
Not yet recruiting NCT06358066 - The Remineralization of Early Enamel Caries in Permanent Teeth Phase 1
Completed NCT03114475 - Effect of CO2 Laser on Enamel White Spot Lesion Formation Around Orthodontic Brackets N/A
Active, not recruiting NCT06403371 - The Effect of Fluoride Varnish on White Spot Lesion in Clear Aligner Orthodontic Patients N/A
Completed NCT05771077 - Effect of Poly Amido Amine Dendrimer, Nano-hydroxyapatite Phase 1