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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02896556
Other study ID # HUDHF-2-Icon
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 31, 2017
Est. completion date April 30, 2022

Study information

Verified date June 2022
Source Hacettepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the esthetic performance of resin infiltration technique on superficial hypo-mineralized and demineralized enamel lesions of anterior teeth


Description:

The teeth that meet the inclusion criteria will be cleaned from debris and clinical intra-oral photos of the lesions will be taken before and after the treatment. Resin infiltration technique will be performed according to manufacturer's instructions under rubber-dam isolation. Intra-oral photos will be taken directly after infiltration (1 day), and 1 week and 6 months later. The system of the Commission Internationale de l'Eclairage (CIE) involving 3 color parameters: lightness (L), red/ green chromaticity (a), and yellow/blue chromaticity (b), will be used to assess the extent and durability of color and lightness changes between lesion and sound enamel areas before and after resin infiltration. The extent of assimilation and durability of effect will be assessed by comparing CIE L*a*b data collected before infiltration (baseline), directly after infiltration (1 day), and 1 week and 6 months later. The color assessments were standardized using a spectrophotometer (SpectroShade, Italy). Lesion areas will be measured for each time point by using an image analysis toolkit (ImageJ, National Institutes of Health, Bethesda, Md.). Multifactorial analysis of variance with repeated measures will be used for statistical analyses.


Recruitment information / eligibility

Status Completed
Enrollment 33
Est. completion date April 30, 2022
Est. primary completion date December 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 7 Years to 17 Years
Eligibility Inclusion Criteria: - Patients and parents of patients who accept to participate and sign the informed consent. - At least one non-cavitated anterior teeth with a superficial discoloration on enamel due to demineralization or hypo mineralization - Fully erupted anterior teeth with closed apices. Exclusion Criteria: - Patients and parents of patients who accept to participate. - Teeth having absence of active cavitated-caries lesions, root canal treatment or restorations - Teeth with ICDAS code 3 lesions (localized enamel breakdown due to caries with no visible dentin) - Teeth that have a previously esthetic procedure (e.g. bleaching) - Patients who are not in cooperation with the procedure. - Fully erupted teeth with open apices

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Resin infiltrate
A resin that used for micro-invasive treatment of enamel-restricted, non-cavitated caries or hypo/demineralized smooth enamel surfaces.

Locations

Country Name City State
Turkey Hacettepe University Ankara

Sponsors (1)

Lead Sponsor Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

References & Publications (3)

Kim S, Kim EY, Jeong TS, Kim JW. The evaluation of resin infiltration for masking labial enamel white spot lesions. Int J Paediatr Dent. 2011 Jul;21(4):241-8. doi: 10.1111/j.1365-263X.2011.01126.x. Epub 2011 Mar 14. — View Citation

Knösel M, Eckstein A, Helms HJ. Durability of esthetic improvement following Icon resin infiltration of multibracket-induced white spot lesions compared with no therapy over 6 months: a single-center, split-mouth, randomized clinical trial. Am J Orthod Dentofacial Orthop. 2013 Jul;144(1):86-96. doi: 10.1016/j.ajodo.2013.02.029. — View Citation

Senestraro SV, Crowe JJ, Wang M, Vo A, Huang G, Ferracane J, Covell DA Jr. Minimally invasive resin infiltration of arrested white-spot lesions: a randomized clinical trial. J Am Dent Assoc. 2013 Sep;144(9):997-1005. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Esthetic success of resin-infiltration technique after 6 months as assessed by spectrophotometry 6 months
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