Effect of Light Curable Resin Modified Glass Ionomer Varnish on Non-Cavitated Proximal Carious Lesions' Progression

Dental Caries Clinical Trial

Official title: The Effect of Light Curable Resin Modified Glass Ionomer Varnish on Inhibiting the Progression of Non-Cavitated Proximal Carious Lesions: A Randomized Controlled Trial

Status Recruiting

Clinical Trial Summary

The standard-of-care preventive measures to stop early tooth decay from becoming worse is by fluoride application, diet counseling, and oral hygiene instructions. This standard way is not always successful. The purpose of this study is to compare standard-of-care preventive measures to stop further tooth decay to standard-of-care preventive measures in addition to a light curable resin modified glass ionomer (RMGI) varnish material (Vanish XT). The material is used for root surface sensitivity treatment, site specific protective coating for newly erupted teeth and other tooth surfaces including early tooth decay.

To be in this study the child must be five to eight years old, medically healthy, attending the Pediatric Dentistry Clinics in King Abdulaziz University Dental Hospital (KAUDH),diagnosed to have at least two primary molars and/ or first permanent molars with early-stage caries (using bitewing radiographs, near infrared digital imaging transilluminaton (NIDIT), and visual assessment), and willing to return for follow up visits. If the child is eligible and the parents agree to the participation of their child in this study, the researcher will review the child's personal and medical history.

The child's two included molars diagnosed with early-stage caries will be randomly assigned to one of two groups: Control Group: will receive standard-of-care preventive measures. Test Group: will receive RMGI varnish application plus the standard-of-care preventive measures. The child will be followed up at six months and 12 months. A dental examination will be done using the same methods used in the first examination to determine whether the caries has become deeper or not. The child may be withdrawn from the study at this point if the caries has become too deep and the tooth will then need a filling.

The child's medical status will be up-dated, reinforcement of oral hygiene instruction and diet counseling will be provided, and fluoride varnish application will be applied to all the teeth in both six and 12 months follow-ups.The RMGI varnish will be reapplied to the test teeth at the six months follow up.

Clinical Trial Description

Materials and Methods Sample:It will be 88 contralateral matched primary molars and/or first permanent molars with non-cavitated proximal carious lesion to be treated in children attending the Pediatric Dentistry Clinics at KAUDH, Jeddah, Saudi Arabia.The included lesions will be randomly allocated in a split-mouth design to be either in the test group or control group:The control group: will be treated with standard-of-care preventive measures which includes application of 5% sodium fluoride (NaF) topical varnish (Vanish 5% Sodium Fluoride White Varnish with Tri-Calcium Phosphate, 3M ESPE, Dental product 44-0007-4718-6-B, St. Paul, MN, 55144-1000 U.S.A. ), oral hygiene instruction, and dietary counseling.The test group: will be treated with light curable RMGI varnish (Vanish™ XT Extended Contact Varnish, 3M ESPE, Dental product 44-0007-4718-6-B, St. Paul, MN, 55144-1000 U.S.A.) in addition to standard-of-care preventive measures.

The Sample size:It was calculated based on the assumptions of odds of caries prevention for the light curable RMGI varnish and the fluoride varnish will be 5.6 and 1.9 respectively based on the literature. The estimated sample is a minimum of 80 pairs (160 lesions) of non-cavitated proximal carious lesions in primary molars and/or first permanent molars are required by the end of the study to detect a statistical difference between the groups at significance level of 0.05 with a power of 80% the sample size was calculated using GPower 3.1 software .To compensate for loss to follow up or other causes of attrition, an additional 10% will be added to the sample size, thus eight pairs will be added with a total of 88 pairs (176 lesions) needed at the start of the study.

Materials and Equipment:

For the lesion diagnosis: Bitewing radiographic examination will be performed using an XCP extension cone paralleling system with photo-stimulable phosphor (PSP) plate biteblocks. The NIDIT examination will be performed using the DIAGNOcam device (DIAGNOcam 2170, Sn 1001941; Kavo). Clinical examination will be performed using mouth mirrors, Community Periodontal Index probe, dental floss without wax, orthodontic elastic separators, a plier for teeth separation for the visual examination, and dental chair light.

Consent and ethical approval:Approval will be obtained from King Abdulaziz University, Research Ethics Committee of the Faculty of Dentistry. The nature of the study will be explained to the parents of the children who meet the inclusion criteria. An informed written consent form will be obtained from all the parents who agree to have their children participate in the study.

Study design:The study design will be a split mouth,triple-blinded, randomized controlled clinical trial following CONSORT guidelines.The teeth will be randomly assigned to one of the two study groups in 1:1 ratio.

Recruitment of the Participants:

Children who are attending the Pediatric Dentistry Clinics in KAUDH during the years 2017 and 2018 over a period of three to six months, who fulfill the subject's inclusion criteria will be initially screened by the primary investigator using bitewing radiographs for the presence of at least two matched bilateral primary molars and/or first permanent molars with non-cavitated proximal carious lesion in the same surfaces. For children who meet all the inclusion criteria, a written consent will be obtained from their parents/guardians to allow their participation in the study. If the subject is diagnosed with more than one qualified pair of lesions, the pairs will be included in the study.

Personal and Medical Information:Before examination, the subject's medical history will be reviewed by the primary investigator along with the age, gender, and nationality.

Lesion Selection and Clinical Assessment:

Radiographic examination:The baseline screening bite-wing radiographs will be taken on both sides of the mouth of the participants . The radiographs will be assessed by two calibrated trained examiners using the following score system: 0: No radiolucency. E1: Radiolucency within outer half of the enamel. E2: Radiolucency in the inner half of the enamel. D1: Radiolucency in the outer third of the dentin. D2: Radiolucency in the middle third of the dentin. D3: Radiolucency in the inner third of the dentin. Disagreements between the first two examiners will be resolved by a third calibrated trained examiner.Teeth that are scored E1, E2, and D1 by two calibrated trained examiners will be included in the study.

Near Infrared Digital Imaging Transillumination: the tooth will be examined by two calibrated trained examiners using the DIAGNOcam according to manufacture instructions. The following scoring system will be used: 0: Sound surface.1: First visible sign of enamel caries. 2: Established enamel caries lesion.3: Established enamel caries lesion with an isolated spot reaching the EDJ.4: Dentin caries penetrating the EDJ lineary. 5: Deep dentin caries lesion. Disagreements between the first two examiners will be resolved by a third calibrated trained examiner. An orthodontic elastic separator will be placed in the corresponding interproximal area to facilitate the subsequent visual examination of the lesion after two days.

Visual Caries Assessment:The orthodontic elastic separators will be removed, and caries will be scored clinically by two calibrated trained examiners using the ICDAS II visual scoring system: 0:clinical sound surfaces 1 and 2: non-cavitated lesions (in 1 air-drying is required to see the lesion and in 2 the lesion is visible without air-drying). 3:Localized enamel breakdown due to caries with no visible dentin. 4:Underlying dark shadow from dentin with or without localized enamel breakdown. 5 and 6:increasing stages of dentine cavitation. Disagreements between the first two examiners will be resolved by a third calibrated trained examiner.Teeth that are scored one and two by two calibrated trained examiners will be included in the study.Other variables that will be recorded at this visit: (1) decayed, missing, filled permeant tooth due to caries (DMFT) and decayed, missing, filled primary tooth due to caries (dmft) score ; (2) plaque score of the included teeth at the time of teeth treatment ; (6) presence of gingival bleeding at the included interproximal site at the time of tooth treatment; (7) and the restoration status of adjacent surface.

Treatment of Lesions: The test group: the lesions will be treated with Vanish XT varnish according to the manufacturer's instructions.

The control group: the lesion will be treated with the Vanish 5% NaF White Varnish according to the manufacturer's instructions. To blind the patient and the parents to which treatment is done to the control tooth, a simulation of the light curable RMGI varnish application will be done, i.e. a thin layer of the fluoride varnish will be applied to the control tooth surface and the light-cure will be held for 20 seconds without turning it on for the purpose of blinding. Then all the teeth will receive an application of the 5% NaF varnish as part of standard of care preventive measures along with oral hygiene instruction and diet counseling.

Follow-up The included subjects will be followed up at six and 12 months for clinical, radiographic, and NIDIT evaluation. At the six months' follow up, the light curable RMGI varnish will be applied in the test group lesions. All the teeth in both groups (test and control) will receive 5% NaF varnish application, along with reinforcement of oral hygiene instruction and diet counseling will be provided.every 6 months. At the six and 12 months follow ups, the subjects will be re-examined as at baseline by two calibrated trained examiners who will be blinded to which treatment group the lesion belongs. Disagreements between the first two examiners will be resolved by a third calibrated blinded examiner. If two of the examiners agree that there is no caries progression, the lesion will be regarded as an arrested lesion. If they agree that there is caries progression, the lesion will be regarded as to have progressed.

Randomization:The subjects will be included after at least one pair of qualified non-cavitated proximal carious lesion meeting the inclusion criteria are identified. Then randomization for the materials for both sides will be done.To ensure the balance of the treatment materials in both sides, block randomization will be generated, different sequence will be randomized for subjects according to the number of molar pairs that will be included in the study in that subject.

Training in the Caries Recording Systems:Inter-examiner and intra-examiner calibration will be done for radiographic, clinical and DIAGNOcam by calibrated examiners. Intra-examiner calibration will be done for DMFT/dmft index. Training will be done until the desired inter- and intra-examiner agreement is achieved.

Statistical analysis:The data will be collected and statistically analyzed using Windows IBM SPSS (Version 22). A P value of < 0.05 will be considered statistically significant. ;

Related Conditions & MeSH terms

• Dental Caries
• Dental White Spot

• NCT number: NCT03685058
• Study type: Interventional
• Source: King Abdulaziz University
• Contact: Najlaa M Alamoudi, BDS,MSc,DSc
• Phone: 00966126402000
• Email: nalamoudi@kau.edu.sa
• Status: Recruiting
• Phase: N/A
• Start date: January 11, 2018
• Completion date: November 2019