Effectiveness of Silver Diamine Fluoride as Cavity Disinfectant After Atraumatic Restorative Treatment in Primary Teeth

Sponsor
Nourhan M.Aly (Other)
Overall Status
Completed
CT.gov ID
NCT03855527
Collaborator
Alexandria University (Other)
60
1
3
14.2
4.2

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the effectiveness of silver diamine fluoride (SDF) compared to chlorhexidine (CHX) as a cavity disinfectant in primary molars after Atraumatic Restorative Treatment approach (ART).

Condition or Disease Intervention/Treatment Phase
  • Drug: Silver Diamine Fluoride
  • Drug: Chlorhexidine
  • Procedure: Atraumatic Restorative Treatment without Disinfection
Phase 2

Detailed Description

This study is a three arm randomized controlled clinical trial, where children with an age range of 4-6 years indicated for Atraumatic Restorative Treatment (ART) are selected from the outpatient clinic of Pediatric Dentistry and Public Health Department, Faculty of Dentistry, Alexandria University after securing necessary consents. Sixty teeth are randomly allocated into 3 groups of Atraumatic restorative treatment approaches. Group I is assigned to silver diamine fluoride as an antibacterial agent, Group II is assigned to chlorhexidine as an antibacterial agent, and Group III serves as a negative control.

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This study is a three arm randomized controlled clinical trial, where children indicated for Atraumatic Restorative Treatment (ART) will be selected.This study is a three arm randomized controlled clinical trial, where children indicated for Atraumatic Restorative Treatment (ART) will be selected.
Masking:
Triple (Participant, Care Provider, Outcomes Assessor)
Masking Description:
The operator will not be blinded to the type of treatment as each antibacterial agent has different consistency, color and application technique. However the expert assessing the microbiologic sample and statistician will be blinded to the treatment groups.
Primary Purpose:
Treatment
Official Title:
Effectiveness of Silver Diamine Fluoride as Cavity Disinfectant After Atraumatic Restorative Treatment in Primary Teeth: A Randomized Clinical Trial
Actual Study Start Date :
Jan 12, 2018
Actual Primary Completion Date :
Jan 18, 2019
Actual Study Completion Date :
Mar 20, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Silver Diamine Fluoride (SDF) group

Atraumatic restorative technique will be performed. Then the cavities will be dried with a gentle flow of compressed air. One drop of silver diamine fluoride (Advantage Arrest Silver Diamine Fluoride 38% - Bottle) will be dispensed into a dappen dish. A micro brush will be bent, dipped into SDF and dabbed on the side of the dappen dish to remove excess liquid before application. SDF will be applied directly to affected tooth surface and dried with gentle flow of compressed air for 1 minute. Excess SDF will be removed with cotton roll. Teeth will be restored with glass ionomer cement (GC Fuji IX).

Drug: Silver Diamine Fluoride
SDF will be applied as a cavity disinfected after atraumatic restorative technique (Antimicrobial effect)
Other Names:
  • SDF
  • Active Comparator: Chlorhexidine group

    Atraumatic restorative treatment will be performed. Then, the cavities will be disinfected by placing a cotton pellet soaked in chlorhexidine solution (Consepsis®2% Chlorhexidine Antibacterial Solution) for 1 minute, air dried and restored using glass ionomer cement.

    Drug: Chlorhexidine
    Chlorhexidine will be applied as a cavity disinfected after atraumatic restorative technique (Antimicrobial effect)
    Other Names:
  • CHG
  • Sham Comparator: Atraumatic Restorative Treatment without Disinfection

    Cavities will be cleaned according to the ART approach.The cavity will be enlarged if needed using sterile hatchet.The carious dentin will be removed with excavators starting at the enamel-dentine junction. The unsupported thin enamel will be fractured off with the hatchet. The caries will be removed carefully until firm dentin is reached (physically resistant to hand excavation). The cavity will be cleaned with wet cotton pellets. Cavities will be restored immediately using conventional glass ionomer cement. All the cavities in the 3 groups will be temporary restored with glass ionomer cement handled according to manufacturer's instructions, however acid etching will not be carried out in order to make sample collection easier following the experimental period.

    Procedure: Atraumatic Restorative Treatment without Disinfection
    Atraumatic Restorative Technique will be performed without cavity disinfection

    Outcome Measures

    Primary Outcome Measures

    1. Microbiological assessment of total viable bacterial count [First day (baseline)]

      The first dentin sample will be collected with a sterile spoon excavator from the firm dentin in the center of the cavity. Two microliters of the samples collected will be inoculated on blood agar for total viable count.

    2. Microbiological assessment of streptococcus mutans count [First day (baseline)]

      The first dentin sample will be collected with a sterile spoon excavator from the firm dentin in the center of the cavity. Two µl of the samples will be inoculated on mitis salivarius agar supplemented with 15 percent sucrose and bacitracin (0.2 U/ml) for selective isolation of Streptococcus mutans.

    3. Microbiological assessment of lactobacilli count [First day (baseline)]

      The first dentin sample will be collected with a sterile spoon excavator from the firm dentin in the center of the cavity.Two µl of the samples will be inoculated on Rogosa agar, a medium selective for Lactobacilli.

    4. Change in the total viable count. [14 days]

      A second dentin sample will be taken from the same position with a sterile round bur for bacteriologic assessment.

    5. Change in the lactobacilli count. [14 days]

      A second dentin sample will be taken from the same position with a sterile round bur for bacteriologic assessment.

    6. Change in the streptococcus mutans count. [14 days]

      A second dentin sample will be taken from the same position with a sterile round bur for bacteriologic assessment.

    Secondary Outcome Measures

    1. Clinical changes in the dentin color [14 days]

      Restoration will be removed and the dentin will be checked using visual-tactile method of examination.

    2. Clinical changes in the dentin consistency [14 days]

      Restoration will be removed and the dentin will be checked using visual-tactile method of examination.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    4 Years to 6 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Children free of any systemic disease or special health care needs.

    • Class I cavity involving dentin in primary molars.

    • Lesion wide enough to allow access of instruments.

    • Informed consent fulfilled.

    Exclusion Criteria:
    • Signs of irreversible pulpitis or pulp necrosis.

    • Patients allergic to silver products.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Faculty of Dentistry, Alexandria University Alexandria Egypt 21512

    Sponsors and Collaborators

    • Nourhan M.Aly
    • Alexandria University

    Investigators

    • Principal Investigator: Lina A Matar, BDS, Alexandria University
    • Study Director: Karin ML Dowidar, PhD, Alexandria University
    • Study Director: Dalia AM Talaat, PhD, Alexandria University
    • Study Director: Dina AE Kholeif, PhD, Faculty of Medicine, Alexandria Univerity

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Nourhan M.Aly, Clinical Instructor and statistician, University of Alexandria
    ClinicalTrials.gov Identifier:
    NCT03855527
    Other Study ID Numbers:
    • SDF as cavity disinfectant
    First Posted:
    Feb 26, 2019
    Last Update Posted:
    Apr 10, 2020
    Last Verified:
    Apr 1, 2020
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Nourhan M.Aly, Clinical Instructor and statistician, University of Alexandria
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 10, 2020