Effectiveness of an ICCMS™ Caries Management Program.

December 15, 2020 updated by: Stefania Martignon, Universidad El Bosque, Bogotá

Effectiveness of an ICCMS™ Caries Management Program. A Schoolchildren Multicenter Randomized Controlled Trial.

The aim of this study is to compare in schoolchildren the effectiveness of an updated caries management program based on the current caries paradigm with the ICCMS™ system (International Caries Classification and Management System) versus an adjusted Colombian dental public health service caries management program, in terms of: 1- caries risk probability, 2- caries lesions, 3- parents' knowledge, attitudes and practices regarding children's oral health.

Null hypothesis: the caries management program based on its current paradigm offers the same degree of effectiveness than the conventional caries management program.

Alternative hypothesis: the caries management program based on its current paradigm offers a different degree of effectiveness than the conventional caries management program.

Study Overview

Status

Completed

Conditions

Detailed Description

This study counts with ethical approval from the Ethics Board in Universidad El Bosque (UEB 008-2014).

Population:

The study population will be 6-7 year-old schoolchildren from the six participant dental schools.

Baseline examination:

The baseline examination will be conducted by the site coordinator examiner. Once the informed consent is signed by the parents and the children give their acceptance, a comprehensive examination will be performed, including:

  • Parents' knowledge, attitudes and practices survey regarding children's oral health.
  • Caries risk probability assessment through individual caries risk assessment plus patient current caries status: low, moderate, high.
  • Radiographic caries detection using the ICCMS™ criteria.
  • Clinical examination:

    • dmf/DMF T/S
    • PUFA Index
    • Dental surface restoration conditions
    • ICCMS™ caries visual detection: Cs: Sound Surfaces (ICDAS code 0); Ci: Initial-stage caries lesion (ICDAS codes 1 y 2); Cm3/Cm4: Moderate-stage caries lesion (ICDAS codes 3-microcavity y 4-dentin shadow) and Ce: Extensive-stage caries lesion (ICDAS codes 5 y 6)
  • Progression assessment of present caries lesions using ICCMS™ criteria in terms of Active or Inactive.

Synthesis and analysis:

The synthesis and analysis of the gathered information will conduce to the ICCMS™ caries management decision plan in terms of caries risk likelihood management and caries lesions management with a structure conservative approach.

This study counts with ethical approval from the Ethics Board in Universidad El Bosque (UEB 008-2014).

Population:

The study population will be 6-7 year-old schoolchildren from the six participant dental schools.

Baseline examination:

The baseline examination will be conducted by the site coordinator examiner. Once the informed consent is signed by the parents and the children give their acceptance, a comprehensive examination will be performed, including:

  • Parents' knowledge, attitudes and practices survey regarding children's oral health.
  • Caries risk probability assessment through individual caries risk assessment plus patient current caries status: low, moderate, high.
  • Radiographic caries detection using the ICCMS™ criteria.
  • Clinical examination:

    • dmf/DMF T/S
    • PUFA Index
    • Dental surface restoration conditions
    • ICCMS™ caries visual detection: Cs: Sound Surfaces (ICDAS code 0); Ci: Initial-stage caries lesion (ICDAS codes 1 y 2); Cm3/Cm4: Moderate-stage caries lesion (ICDAS codes 3-microcavity y 4-dentin shadow) and Ce: Extensive-stage caries lesion (ICDAS codes 5 y 6)
  • Progression assessment of present caries lesions using ICCMS™ criteria in terms of Active or Inactive.

Synthesis and analysis:

The synthesis and analysis of the gathered information will conduce to the ICCMS™ caries management decision plan in terms of caries risk likelihood management and caries lesions management with a structure conservative approach.

The first step of the management plan considers the caries risk likelihood.

The management options include:

  • Low likelihood: Tooth brushing 2/day with a fluoride toothpaste (≥1,000 ppm F-), following the dental team instructions; motivational engagement (discuss with patients how to improve oral health behaviors - including amount of sugar); cross-brushing for erupting first molars; use of dental floss; recalls every 6 months, including professional cleaning.
  • Moderate likelihood: Previous activities plus prescribed F- mouthrinse; sealants in caries risk surfaces, F- varnish 2 times/year; motivational interviewing; recalls every 3 months, including professional cleaning.
  • High likelihood: Previous activities and increase F- varnish to 4 times/year plus Topical F- application; counseling: reduce sugar amount & frequency; recalls every 3 months, including professional cleaning.

The patient's caries risk factors management plan is tailored at the individual level and involves actions to protect sound tooth surfaces from developing new caries lesions, and all current active and inactive lesions from progressing. In addition, it aims at lowering the caries risk likelihood of the patient when moderate or high, and to maintain it if low.

The second step is the caries diagnosis decision making at the surface level which conducts to the surface diagnosis decision matrix. This decision relies on the clinical classification of dental caries using ICCMS™ criteria and the radiographic extent of the lesion (enamel or dentin) plus the activity status of the lesions. Only active caries lesions require caries management. The level of intervention depends on the clinical caries classification of the surface or tooth and the radiological extent (when information is available) of the lesion in enamel or dentin. Management levels of active caries lesions are classified as follows:

  • MInitial: Initial caries management stage (non-operative care (NOC)-control)
  • MModerate: Moderate caries management stage (minimally invasive surgical caries management with no or minimal dentin removal)
  • MExtensive: Extensive caries management stage (invasive surgical caries management with dentin removal).

For sound surfaces, risk based prevention is performed. For inactive lesions, restorations might be performed depending on esthetic and plaque retention reasons.

Intervention:

The children will be randomized in two groups as follows:

Group A (Experimental): ICCMS™ caries management according to the surface diagnosis decision matrix of active Ci, Cm3/4, and Ce caries lesions. Individual management according to the future patient caries risk likelihood with specific prevention strategies.

Group B (Control): conventional caries management. Operative treatment of Cm and Ce caries lesions (caries shadows and cavities) with conventional restorative treatment. Systematic caries risk management with twice-a-year fluoride gel application, sealants on all occlusal surfaces and oral health literacy.

When the management plan is finalized in both groups, patients must continue attending the clinic according to their group for the following three years.

Follow-up assessments will be conducted at one and three years after baseline, with the baseline indicators as described above.

Study Type

Interventional

Enrollment (Actual)

240

Phase

  • Not Applicable

Contacts and Locations

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

Study Locations

    • D.c:
      • Bogotá, D.c:, Colombia, 11001
        • Universidad El Bosque

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

6 years to 7 years (CHILD)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Children from 6 to 7 years old
  • Informed consent signed
  • Children in standard good general health

Exclusion Criteria:

  • Children with physical disability and/or cognitive diseases
  • Children whose family will is planning to move from the city in the following 36 months
  • Children with orthopedic/orthodontic appliances at baseline

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

  • Primary Purpose: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: DOUBLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Experimental group
caries management based on the ICCMSTM: Patient intervention according to the caries risk likelihood: high, moderate or low. Surfaces intervention according to the surface diagnosis decision matrix (ICCMSTM): Mi: Initial caries management, Mm: Moderate caries management, and Me: Extensive caries management.
Caries management based on the ICCMSTM: Patient intervention according to the caries risk likelihood: high, moderate or low. Surfaces intervention according to the surface diagnosis decision matrix (ICCMSTM): Mi: Initial caries management, Mm: Moderate caries management, and Me: Extensive caries management.
Other Names:
  • ICCMS™ group
ACTIVE_COMPARATOR: Control group
Systematic patient caries risk intervention (all managed as high risk patients). Surfaces intervention with conventional caries management of cavitated/dentin caries lesions (restorative treatment).
Systematic patient caries risk intervention (all managed as high risk patients). Surfaces intervention with conventional caries management of cavitated/dentin caries lesions (restorative treatment).
Other Names:
  • Colombian Health System

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evolution of ICCMSTM caries likelihood after 1 and 3 years.
Time Frame: up to 36 months
Change in ICCMSTM caries likelihood subjects' distribution after 1 and 3 years
up to 36 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Presence of new caries lesions in terms of ICCMSTM categories after 1 and 3 years.
Time Frame: up to 36 months
Change in the presence of new caries lesions in terms of ICCMSTM categories after 1 and 3 years.
up to 36 months
Number of appointments after 1 and 3 years.
Time Frame: up to 36 months
Total number of appointments after1 and 3 years.
up to 36 months
Progression of existing caries lesion in terms of ICCMSTM categories after 1 and 3 years.
Time Frame: up to 36 months
Change in the progression of existing caries lesion in terms of ICCMSTM categories after 1 and 3 years.
up to 36 months

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Stefania Martignon, PhD, UNICA - Unidad de Investigación en Caries, Facultad de Odontología

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)

March 1, 2014

Primary Completion (ACTUAL)

November 1, 2017

Study Completion (ACTUAL)

May 1, 2019

Study Registration Dates

First Submitted

May 10, 2019

First Submitted That Met QC Criteria

December 15, 2020

First Posted (ACTUAL)

December 19, 2020

Study Record Updates

Last Update Posted (ACTUAL)

December 19, 2020

Last Update Submitted That Met QC Criteria

December 15, 2020

Last Verified

December 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • 008-2014

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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