Colorimetric, Ultra-structural and Elemental Comparison of Dental Enamel Defects (COLOEMAIL)

October 17, 2022 updated by: Assistance Publique - Hôpitaux de Paris

Colorimetric Comparison of Email Defects Using Spectrophotometric and Computer Techniques and Biological, Structural and Physico-chemical Analyses of Teeth or Pathological Enamel

The study focuses on the analysis of enamel defects grouping together hypomineralization and hypoplasia. It focuses on 3 very characteristic enamel pathologies that are most often encountered in dental consultations: Molar Incisor Hypomineralization (MIH), dental fluorosis (FD) and amelogenesis imperfecta (AI). The research focuses on the use of a spectrophotometer for measuring tooth colors: the Zfx SpectroShade® (MHT) and its software as a means of early diagnosis of pre-eruptive enamel abnormalities. The main objective of the study is to analyze the color parameters of teeth affected with one of the 3 enamel abnormalities for use of the spectrophotometer as a non-invasive diagnostic tool for enamel defects.

The secondary objective is focused on the biological, structural and physicochemical characterizations of these different enamel pathologies from extracted teeth or enamel biopsies that must be ground to achieve a restoration.

Study Overview

Detailed Description

Methodology:

V1 inclusion visit (D1):

The subjects will be screened during a consultation carried out as part of the treatment in the participating dentistry departments. The inclusion and non-inclusion criteria for participants will be verified and the study will be offered to eligible patients and controls. The research briefing note will be given and the non-objection of the participants (adults and representative (s) of parental authority) will be collected. The investigator will then take the photographs and spectrophotometer shots (at least 2 teeth per participant).

V2 follow-up visit (within 2 months of the inclusion visit (D2 to M2)):

The patients will be reviewed in consultation as part of the treatment for selective grinding for dental restoration or extraction (if the tooth (s) is (are) no longer storable). The teeth or pathological enamel samples will be recovered and centralized at the Laboratory of Oral Molecular Physiopathology.

Biological, structural and physico-chemical analyzes will be carried out from these samples.

In order to ensure follow-up of participants, the principal investigator of each center will maintain a correspondence table including the participant's identity and his research identification number. He will also keep a register of oppositions up to date.

The subject's opposition or participation will be notified in his medical file. A copy of the briefing notes and non-objection forms signed by the dentist will be kept on site with the research documents. Minors who become adults during their participation will benefit from appropriate information and their non-objection will be collected.

Primary endpoint Analysis, using the spectrophotometer, of the numerical values of the color of the teeth in each of the populations studied (Hereditary amelogenesis imperfecta (AIH), dental fluorosis (FD), Hypomineralization Incisors and Molar (MIH) and control).

For each pathology, the values of these parameters will be compared. Secondary endpoints

  • Intra-pathology classification according to the severity of each pathology.
  • Characterization and biological, structural and physicochemical analysis of these different pathologies from extracted teeth or enamel biopsy to be ground to achieve a restoration.

Sample analysis The teeth samples will be stored at room temperature in the Oral Molecular Physiopathology laboratory in the Research Center.

During the research, biological, structural and physicochemical analyzes will be carried out at the laboratory or in another laboratory in France or abroad. A contract will be established upstream of these analyzes with the partner laboratory.

At the end of the research, samples not destroyed by destructive analysis techniques will be embedded in the resin and stored for 10 years before being destroyed. These samples can be used for additional analyzes (biological, structural and physico-chemical) according to the request of the references for the publication process.

Study Type

Observational

Enrollment (Anticipated)

80

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Paris, France, 75013
        • Recruiting
        • Service d'odontologie, Hôpital Pitié-Salpêtrière
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

8 years to 55 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Major or minor patients with Hereditary Imperfect Amelogenesis Imperfecta (HIA), Dental Fluorosis (DF), Incisor and Molar Hypomineralization (MIH) or Control

Description

For patients :

Inclusion Criteria :

  1. Age between 8 and 55 years old
  2. Carrier of one of the following 3 quantitative pre-eruptive enamel anomalies : AIH, dental fluorosis or MIH
  3. Information and collection of the non-opposition of the adult patient or of the representative(s) of parental authority present for the minors.

Criteria for non-inclusion :

  1. Pregnant or breastfeeding woman
  2. Under guardianship or curators
  3. Opposition of the minor patient
  4. Presenting pre-eruptive anomalies only on the molars (the spectrophotometer can only take pictures of the anterior dental sector (incisors and canines)).
  5. Other types of hypomineralization (post-eruptive, of traumatic or infectious origin, idiopathic).
  6. Having undergone radiotherapy or chemotherapy inducing dental and periodontal damage.
  7. Having systemic abnormalities (unbalanced diseases), haemochromatosis, porphyria
  8. Under medication likely to disturb the coloring of the teeth

For witnesses :

Inclusion Criteria :

  1. Age between 8 and 55 years old
  2. Information and collection of the non-opposition of the adult witness or of the representative(s) of parental authority present for the minors.
  3. Free of any anomaly of tooth structure, exogenous dyschromia and carious lesions.

Criteria for non-inclusion :

  1. Pregnant or breastfeeding woman
  2. Under guardianship or curators
  3. Opposition of the minor witness
  4. Carrier of a quantitative pre-eruptive enamel anomaly
  5. Polycarpus (preventing the diagnosis of amyl hypomineralization)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Other
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
spectrophotometer, and numerical values of tooth color in the populations studied
at the first visit Shooting with Spectrophotometer and at the second visit for all patients except control population: Tooth extraction or restorative treatment Collection of teeth or enamel debris for analysis
  • Calibration of the spectrophotometer (calibration of white and green color on the provided support),
  • Placing the patient or witness in the chair,
  • Placement of intraoral retractors,
  • Photographs of the dental arch in occlusion as well as slightly open mouth to visualize the mandibular incisors,
  • If MIH is suspected, occlusal images of the occlusal surfaces of the first molars will be taken with the help of a dental mirror,
  • Shooting with the spectrophotometer centered on each of the teeth of interest in the anterior sector with verification of the good quality of the shot according to the axis (validated in green on the camera),
  • Backup of images with coded identification number
  • Chemical analysis of enamel mineral.
  • Techniques of spectrometry and spectroscopy (Raman and FTIR)
  • Atomic Probe Tomography and Protein Mass Spectrometry (ICP-MS).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
analyze the color parameters of teeth presenting one of the 3 enamel anomalies in order to use the spectrophotometer as a non-invasive diagnostic tool for enamel dyschromia.
Time Frame: at the first visit = inclusion visit
at the first visit = inclusion visit

Secondary Outcome Measures

Outcome Measure
Time Frame
Biological characterization of the proteins of the dental enamel matrix by Western Blot and/or mass spectrometry from samples (extracted teeth or enamel biopsies to be ground during the treatment).
Time Frame: at the second visit, 2 months after inclusion visit and after tooth extraction
at the second visit, 2 months after inclusion visit and after tooth extraction
Ultra-structural characterization under electron microscope and biomechanics by nanoindentation of enamel pathologies from extracted teeth or enamel biopsies to be ground during the treatment.
Time Frame: at the second visit, 2 months after inclusion visit and after tooth extraction
at the second visit, 2 months after inclusion visit and after tooth extraction
Physico-chemical characterization by different spectroscopic techniques of enamel pathologies from extracted teeth or enamel biopsies to be ground during the treatment.
Time Frame: at the second visit, 2 months after inclusion visit and after tooth extraction
at the second visit, 2 months after inclusion visit and after tooth extraction
Physico-chemical characterization by atomic probe tomography of enamel pathologies from extracted teeth or enamel biopsies to be ground during the treatment.
Time Frame: at the second visit, 2 months after inclusion visit and after tooth extraction
at the second visit, 2 months after inclusion visit and after tooth extraction

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 18, 2022

Primary Completion (Anticipated)

July 18, 2024

Study Completion (Anticipated)

September 18, 2024

Study Registration Dates

First Submitted

December 18, 2020

First Submitted That Met QC Criteria

January 7, 2021

First Posted (Actual)

January 11, 2021

Study Record Updates

Last Update Posted (Actual)

October 18, 2022

Last Update Submitted That Met QC Criteria

October 17, 2022

Last Verified

October 1, 2022

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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