12 Month Follow up in Vivo Icon Study on Fluorotic Teeth

Fluorosis Clinical Trial

Official title:

In Vivo Action of Infiltrating Resin Icon® on Fluorosis - a 12 Month Follow up Trial

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT02925780
• Other study ID #: RIAFLUOR
• Status: Withdrawn
• Phase: N/A
• Start date: December 2019
• Est. completion date: December 2021

Study information

• Verified date: June 2023
• Source: DMG Dental Material Gesellschaft mbH
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Clinical trial to investigate the clinical efficiency of resin infiltration compared to microabrasion in the improvement of dental fluorosis.

Description:

Dental fluorosis is an endemic public health concern that develops if infants are subjected to excessive amounts of fluoride during enamel formation. Anatomopathologically, dental fluorosis presents itself as a hypermineralized surface layer and subsurface hypomineralization involving the external third of the thickness of the enamel, which is equivalent to early carious lesions. In addition, fluorosis features a number of clinical changes in the enamel surface, ranging from the appearance of thin white lines up to severe structural defects, thereby compromising overall esthetics, which sometimes leads to children dropping out of school due to its psychological impact. The aim of this controlled clinical trial is to evaluate the efficacy of enamel microabrasion and resin infiltration in improving the dental esthetic of patients with fluorosis. Resin infiltration is a microinvasive technique that can improve the esthetics by infiltrating a low-viscosity resin (that has a similar refractive index to enamel) into the porose hypomineralized enamel of fluorosed white spots. This approach thus largely preserves the enamel compared to more invasive techniques such as microabrasion and has been shown to be efficient in previous studies. This study will be conducted in the provinces of Pichincha and Cotopaxi, Ecuador and patients between 10 to 12 years of age with stage 1, 2, and 3 fluorosis according to the Thylstrup and Fejerskov (TF) scale or questionable, very mild, and mild fluorosis according to Dean's Index will be recruited. In addition to the immediate esthetic improvement, long term stability of the outcome will be assessed at 3, 6 and 12 months.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: December 2021
• Est. primary completion date: June 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 10 Years to 12 Years

Eligibility

Inclusion Criteria:

• Questionable, Very mild, and Mild (Dean's Index) dental fluorosis as well as TF scale grades 1, 2, and 3 of the upper anterior teeth.
• Parents of children who accept and commit to the informed consent letter collaborate with the study taking their children to each of the scheduled follow ups.

Exclusion Criteria:

• Teeth without fluorosis.
• Teeth with hypoplasia.
• Teeth with incipient caries lesions observed at gingival level and differentiated by the Presence of plaque.
• Teeth previously restored or with aesthetic corrective treatments
• Teeth with endodontic treatment.
• Patients with low or questionable hygiene.
• Malnourished patients or that have some underlying disease.
• Teeth with less than two thirds of its visible crown.
• Children that have less than six teeth in their oral cavity.
• Allergic reaction to methylmethacrylate.

Related Conditions & MeSH terms

• Fluoride Poisoning
• Fluorosis
• Fluorosis, Dental
• Oral Deseases

Intervention

Device:
• Resin infiltration
Teeth selected for this group will be treated with the resin infiltrant Icon according to the manufacturer's instructions. In short, teeth will be isolated with a rubber dam and the labial tooth surface cleaned with non-fluoride prophylactic paste and pumice. After an etching and drying step (to open the lesion surface), Icon will be applied following the manufacturer's instructions and subsequently light cured, followed by polishing. Digital images are taken before and after the treatment as well as at the follow-up visits (3, 6, 9 and 12 months).
• Microabrasion
The labial surfaces of teeth selected for this group will be isolated and precleaned. Subsequently, the microabrasive material, Opalustre, will be applied according to the manufacturer's instructions, using a rubber cup at low speed (5 times each for 5 seconds). Between each of the applications the surface is washed by flushing water using a syringe. Digital images are taken before and after the treatment as well as at the follow-up visits (3, 6, 9 and 12 months).

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
DMG Dental Material Gesellschaft mbH

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	action of DMG Icon-infiltrative ® resin and micro abrasion to mask fluorotic enamel	Evaluate the action of DMG Icon-infiltrative resin and micro abrasion immediately after application to mask fluorotic teeth by comparison of pre- vs. post-treatment photographs	immediate after treatment
Secondary	Surface changes	changes that occur on the surface of the teeth with fluorosis, which have been treated with DMG Icon ® and micro-abrasion assessed via photographs	12 month
Secondary	Clinical characteristics Icon	clinical characteristics of the tooth surfaces that have been treated with DMG Icon ® and micro-abrasion and its relationship to the degree of fluorosis	3, 6, 9, 12 month
Secondary	Efficacy of infiltration to mask fluorotic teeth long-time	Compare the benefit of the infiltrative resin DMG Icon related to micro abrasion Opalustre ULTRADENT as control procedure, focus: stabilisation of masking quantified by photographs	12 month