Cariostatic and Remineralizing Effects of Three Different Dental Varnishes

Sponsor
Nisreen Ibrahim khan (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04887389
Collaborator
(none)
115
1
3
17
6.8

Study Details

Study Description

Brief Summary

This study is a randomly, controlled, prospective in vivo study.

The objective of this study is:

To evaluate the cariostatic and re-mineralizing effects of Nano silver fluoride, Nano

Hydroxyapatite and sodium fluoride varnishes in caries prevention through:
  1. Clinical evaluation using international caries detection and assessment system (ICDAS II visual scoring criteria)

  2. Calcium and fluoride content using enamel biopsy

Condition or Disease Intervention/Treatment Phase
  • Drug: Nano Silver Fluoride varnish
  • Drug: nano-hydroxyapatite varnish
  • Drug: sodium Fluoride Varnish
Phase 4

Detailed Description

Dental caries is a chronic, multi factorial, transmissible, infectious disease. Caries prevalence in young children in Egypt is very high, and most of the decayed teeth are left untreated, The increase prevalence of dental caries in children globally and in developing countries such as Egypt particularly makes the need for preventive treatment is necessary, one of the ways to prevent dental caries is the application of fluoride which can prevent dental caries by inhibiting demineralization of the crystal structures inside the tooth and enhancing remineralization.

Subsequently over the years various topical fluoride agents have been evolved but NaF (a 22,600 ppm F- preparation) is the most commonly used agent, Based on systematic studies, 5% NaF varnish was more effective in re-mineralizing early enamel caries.

Another anti caries product is a nano-hydroxyapatite (n-HAP), it has antibacterial effect, higher solubility, surface energy and bio activity, there are several studies concluded that 10% (n-HAP) may be optimal for remineralization of early enamel caries Nano-Silver Fluoride (NSF) is a new experimental formulation containing silver nanoparticles, it was introduced by Targino AG et al.(2014) to combat the problem of black discoloration of Silver Diamine Fluoride. It is safe to be used in humans and has effective antimicrobial properties against the pathogens responsible for the development of dental caries.

most of the studies have been evaluated the effectiveness of anti-caries agent in In Vitro and to the best of our knowledge, there are no published studies in Egypt on the effectiveness of these agent. As such, due to the continuous development of new remineralizing agents, research is needed to investigate the newer remineralizing agents under different circumstances. The present study will be carried out to evaluate the efficacy of Nano silver fluoride, Nano Hydroxyapatite and Sodium fluoride varnishes in caries prevention.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
115 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Selected children will be divided randomly into three groups: Group 1: Children receiving Nano Silver Fluoride varnish (NSF) (n =39). Group 2 Children receiving Nano-hydroxyapatite varnish (n = 37). Group 3: Children receiving Sodium Fluoride Varnish (n = 39) Procedure for material application The application of single drop (0.1 mL) of either (5%) NSF, (10%) n-HAP, (5%) NaF varnishes with a disposable micro-applicator tip for 10 seconds. NSF will be used in a single application and no repetition. While n-HAP, NaF varnishes will be applied each 6 months .Selected children will be divided randomly into three groups:Group 1: Children receiving Nano Silver Fluoride varnish (NSF) (n =39). Group 2 Children receiving Nano-hydroxyapatite varnish (n = 37). Group 3: Children receiving Sodium Fluoride Varnish (n = 39) Procedure for material application The application of single drop (0.1 mL) of either (5%) NSF, (10%) n-HAP, (5%) NaF varnishes with a disposable micro-applicator tip for 10 seconds. NSF will be used in a single application and no repetition. While n-HAP, NaF varnishes will be applied each 6 months .
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Cariostatic and Remineralizing Effects of Three Different Dental Varnishes (A Clinical Trial)
Actual Study Start Date :
Aug 1, 2021
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Jan 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group of • Nano Silver Fluoride varnish ( NSF)

Selected children will be divided randomly into three groups: Group 1: Children receiving Nano Silver Fluoride varnish (NSF) (n =50).

Drug: Nano Silver Fluoride varnish
Nano Silver Fluoride(5%) is a new experimental formulation containing silver nanoparticles, chitosan and fluoride combines preventive and antimicrobial properties. It is a yellow solution and safe to be used in humans
Other Names:
  • ( NSF)
  • Experimental: group of Nano hydroxyapatite varnish (n-HAP)

    Group 2 Children receiving Nano-hydroxyapatite varnish (n = 50)

    Drug: nano-hydroxyapatite varnish
    nano-hydroxyapatite (10%) has antibacterial effect, higher solubility, surface energy and bioactivity and its structure is similar to dental apatite.
    Other Names:
  • (n-HAP)
  • Experimental: group of Sodium Fluoride Varnish (NaF)

    Group 3: Children receiving Sodium Fluoride Varnish (n = 50)

    Drug: sodium Fluoride Varnish
    Fluoride varnish (5%) applied every six months is effective in preventing caries in the primary and permanent dentition of children and adolescents
    Other Names:
  • NaF
  • Outcome Measures

    Primary Outcome Measures

    1. a. Clinical evaluation using international caries detection and assessment system (ICDAS II visual scoring criteria [1. All children will be assessed clinically in four visits along one year, at the baseline as well as at 3rd, 6th and 12th month of follow up visit]

      After taking the personal data of the participant, dental examination will be conducted by one trained and calibrated examiner under the standard situation including semi-supine position of the subject, good illumination and taking into account all methods of infection control. Baseline dental examination for all surfaces of included teeth according to ICDAS II was recorded. Only the surfaces with 0, 1 and 2 score will be included in the follow up assessment (Drying of the tooth surface is the key for detecting non-cavitated lesions). Diagnostic criteria for newly dental caries : In order to compare the preventive efficacy of the three preventive agent, any change in the baseline recording of score 0, 1, or 2 will be recorded in each visit of all three groups, and an comparison will be made between the mean of tooth surfaces with score 0, 1 or 2 in the baseline visit and during all follow-up visits in each group and after that comparing among all groups.

    2. Enamel biopsy for detecting Calcium and Fluoride content . [Fluoride and calcium content will be evaluated at the baseline as well as at the last follow-up visit through study completion, an average of 1 year"]

      The tooth on which the biopsy had to be done will be isolated with the help of cotton rolls and high volume suction to eliminate any chances of saliva contamination. Sticking plaster will be used to cover the tooth to be subjected for biopsy. A 6 mm circular punch will be made in the sticking plaster keeping in mind that it should be present on the buccal surface of molar. A 6 mm non-fluoride containing circular blotting paper will wetted with 5 µL of 30% phosphoric acid and immediately placed on the punched window for 4 s . This filter paper will then transferred to plastic tube which had 0.1 ml of double distilled water pipetted using a micro-pipette. Equal amount of total ionic strength adjustment buffer (TISAB-II) will added using a micropipette to the plastic tube, after which it will be stored for 3 days. After that it will send to laboratory for fluoride and calcium analysis.At the end -fluoride varnish will be applied to the surface.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    7 Years to 10 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • The inclusion criteria of participated children :
    1. Age rang 7-10 years.

    2. Teeth with score 0, 1 or 2 according to (international caries detection and assessment system) ICDAS II index.

    3. Patient did not receive any re-mineralizing agent other than the regular toothpaste during the past three months.

    4. No known history of allergy against silver particles or colophonium.

    5. written informed consent from the parents/guardians.

    Exclusion Criteria:
    1. Teeth with score 3 or more according to ICDAS II index.

    2. Partially erupted permanent teeth.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Faculty of Dentistry / Mansoura University Mansoura Dakahlia Egypt 35511

    Sponsors and Collaborators

    • Nisreen Ibrahim khan

    Investigators

    • Principal Investigator: Salwa A Hegazy, PhD, Head of Dental Public Health department

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Nisreen Ibrahim khan, Lecturer of Dental Public Health and Preventive Dentistry, Mansoura University
    ClinicalTrials.gov Identifier:
    NCT04887389
    Other Study ID Numbers:
    • A07071020
    First Posted:
    May 14, 2021
    Last Update Posted:
    Jun 8, 2022
    Last Verified:
    Jun 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by Nisreen Ibrahim khan, Lecturer of Dental Public Health and Preventive Dentistry, Mansoura University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 8, 2022