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Clinical Trials/NCT06362681
NCT06362681
Recruiting
Not Applicable

Randomized Clinical Trial to Evaluate the Effectiveness of Three Remineralizing Agents on Mineral Density in Permanent Teeth and Molars With Molar Incisor Hypomineralization

Universidad Nacional Autonoma de Mexico1 site in 1 country100 target enrollmentMarch 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Molar Incisor Hypomineralization
Sponsor
Universidad Nacional Autonoma de Mexico
Enrollment
100
Locations
1
Primary Endpoint
Mineral Density
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The aim of this study was to present a comparative evaluation of the long-term efficacy of fluoride varnish( Flúor protector), Clinpro™ White Varnish and pastes containing CPP-ACP in the remineralization of creamy-white and yellow brown defects in incisors and permanent first molars with Molar Incisor Hypomineralization (MIH) in schoolchildren 6-12 years-old in Mexico.

Detailed Description

The study included 208 teeth with yellow-brown or creamy-white defects in children aged 6-12 years who were newly diagnosed with MIH with no substance loss or caries or prior restorative treatment. The children will be randomly divided into the experiment groups: control (oral hygiene motivation only), fluoride varnish, clinpro white Varnish and pastes containing CPP-ACP and followed up for 24 months. The evaluations will be made based on the ICDAS criteria and the measurements which were performed using the laser fluorescence method (DIAGNOdent, KaVo, Biberach, Germany) in the follow-ups.

Registry
clinicaltrials.gov
Start Date
March 1, 2024
End Date
March 30, 2026
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Universidad Nacional Autonoma de Mexico
Responsible Party
Principal Investigator
Principal Investigator

Alvaro García Perez

Dr.

Universidad Nacional Autonoma de Mexico

Eligibility Criteria

Inclusion Criteria

  • Children between 6 to 12 years
  • They live in the selected study area
  • Have at least one permanent incisor or molar with mild or moderate MIH (creamy white and/or yellow or brown opacities)
  • That their parents authorize participation in the study through informed consent.
  • No proven or suspected allergy and/or sensitivity to milk protein, as it is a component of the CPP-ACP product.

Exclusion Criteria

  • Defects in enamel development related to syndromes, dental fluorosis, amelogenesis imperfecta, dentinogenesis imperfecta.
  • Presence of orthodontic appliances.
  • Teeth with MIH with restorations, or severe MIH (affected enamel develops post-eruptive enamel breakdown), or carious lesions classified as score \>0 according to the ICDAS.
  • Children who do not show cooperation in the use of remineralizing agents.

Outcomes

Primary Outcomes

Mineral Density

Time Frame: 24 months

evaluate and compare variations in mineral density (MD) using laser induced fluorescence (LF) after applying Fluoride Varnish, Clinpro or Casein phosphopeptide amorphous calcium phosphate on teeth with Molar Incisor Hypomineralization (MIH).

Study Sites (1)

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