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
About this trial
This is an interventional treatment trial for Caries,Dental
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
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
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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