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Non-invasive Caries Management: Clinical Study (NICM)

Primary Purpose

Caries,Dental, Caries Arrested

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Resin Infiltration
Sodium Fluoride Varnish
Sponsored by
Western University, Canada
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Caries,Dental

Eligibility Criteria

15 Years - 50 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients must present at least two non-cavitated proximal caries lesions
  • Patients must be able to give informed consent in English
  • Patients must be resident in London, Ontario, or nearby locales with community fluoridation

Exclusion Criteria:

  • Patients presenting proximal caries that are beyond the outer third of dentin
  • Patients suffering from a disability that impairs dental hygiene performance
  • Patients that are unable to perform her/his own oral hygiene

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Resin Infiltration

    Sodium Fluoride Varnish

    Arm Description

    The interproximal surface with initial dental caries that are selected for this group will be treated using the resin infiltration ICON (DMG, Germany) and 5% Sodium Fluoride Varnish

    The interproximal surface with initial dental caries that are selected for this group will be treated using topical application of 5% Sodium Fluoride Varnish.

    Outcomes

    Primary Outcome Measures

    Caries lesion progression
    Evaluate caries lesion progression after using DMG Icon-infiltrative resin and/or 5% NaF Varnish by comparison of baseline and one year post-treatment radiographics.

    Secondary Outcome Measures

    Caries risk assessment
    Evaluate non-invasive and minimally-invasive therapies on the progression of the caries lesions correlated with the patient's caries risk.

    Full Information

    First Posted
    April 28, 2020
    Last Updated
    May 4, 2020
    Sponsor
    Western University, Canada
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04373356
    Brief Title
    Non-invasive Caries Management: Clinical Study
    Acronym
    NICM
    Official Title
    Non-invasive and Minimal Intervention in Dental Caries Management: Randomized Clinical Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2020
    Overall Recruitment Status
    Unknown status
    Study Start Date
    July 1, 2020 (Anticipated)
    Primary Completion Date
    October 30, 2021 (Anticipated)
    Study Completion Date
    November 30, 2021 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Western University, Canada

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    Clinical trial to compare non-invasive and minimally-invasive therapies on the progression of the caries lesions. Clinical investigation of resin infiltration versus sodium fluoride (5% NaF) varnish application.
    Detailed Description
    Dental caries is the most globally prevalent disease that affects thousands of adults and children. Caries is a biofilm-mediated, sugar-driven, multifactorial, and dynamic disease that results from the imbalance between demineralization and remineralization of the dental hard tissues. Preventing the onset of the disease should be the primary goal; however, once the disease is present efforts should be made by both patient and clinician to successfully reestablish the mineralization balance by the use of preventive and/or minimally-invasive methods when possible. The sodium fluoride (5% NaF) varnish is one of the most common therapies used as a non-invasive approach for caries prevention and remineralization; and, the resin infiltration materials are indicated for the minimal intervention of non-cavitated occlusal and proximal caries. The minimal intervention has been considered the new concept of caries management. Although several studies discussing minimal intervention or non-intervention are available, there is a lack of published randomized controlled trials (RCTs) providing data about the use of non-invasive therapies on incipient lesions, and its correlation with the patient's caries risk. The aim of this study is to evaluate the efficacy non-invasive and minimally-invasive therapies on the progression of the caries lesions considering the patient's caries risk. This study will be conducted in the province of Ontario, Canada. A total of thirty patients (15 to 50 years old), who present with a minimum of two incipient proximal carious lesions on the proximal surfaces of posterior teeth (non-cavitated lesions identified as small, faint radiolucent areas seen on the intra-oral radiographs) will be asked to participate in this study. The radiologic assessment of incipient lesions will be performed by a dental radiologist, blinded to the selected treatment groups, by comparison of the radiographs imaging over time.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Caries,Dental, Caries Arrested

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    30 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Resin Infiltration
    Arm Type
    Experimental
    Arm Description
    The interproximal surface with initial dental caries that are selected for this group will be treated using the resin infiltration ICON (DMG, Germany) and 5% Sodium Fluoride Varnish
    Arm Title
    Sodium Fluoride Varnish
    Arm Type
    Active Comparator
    Arm Description
    The interproximal surface with initial dental caries that are selected for this group will be treated using topical application of 5% Sodium Fluoride Varnish.
    Intervention Type
    Device
    Intervention Name(s)
    Resin Infiltration
    Intervention Description
    Patients will be instructed about enhancing their oral hygiene, and will be asked to brush their teeth twice a day with fluoride toothpaste, and use dental floss daily. In short, teeth will be isolated with a rubber dam and ICON will be applied following the manufacturer's instructions. After that, the rubber dam will be removed and 5% NaF Varnish will be applied. Standardized digital bitewing radiograph will be taken at baseline and one year after treatment for caries lesion progression comparison.
    Intervention Type
    Device
    Intervention Name(s)
    Sodium Fluoride Varnish
    Intervention Description
    Patients will be instructed about enhancing their oral hygiene, and will be asked to brush their teeth twice a day with fluoride toothpaste, and use dental floss daily. In short, teeth will be isolated with cotton roll and 5% NaF varnish will be applied following the manufacturer's instructions. Standardized digital bitewing radiograph will be taken at baseline and one year after treatment for caries lesion progression comparison.
    Primary Outcome Measure Information:
    Title
    Caries lesion progression
    Description
    Evaluate caries lesion progression after using DMG Icon-infiltrative resin and/or 5% NaF Varnish by comparison of baseline and one year post-treatment radiographics.
    Time Frame
    One year follow up
    Secondary Outcome Measure Information:
    Title
    Caries risk assessment
    Description
    Evaluate non-invasive and minimally-invasive therapies on the progression of the caries lesions correlated with the patient's caries risk.
    Time Frame
    One year follow up

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    15 Years
    Maximum Age & Unit of Time
    50 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients must present at least two non-cavitated proximal caries lesions Patients must be able to give informed consent in English Patients must be resident in London, Ontario, or nearby locales with community fluoridation Exclusion Criteria: Patients presenting proximal caries that are beyond the outer third of dentin Patients suffering from a disability that impairs dental hygiene performance Patients that are unable to perform her/his own oral hygiene

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Non-invasive Caries Management: Clinical Study

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