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Clinical Trials/NCT04213573
NCT04213573
Suspended
Phase 2

Parental Perception of Silver Diamine Fluoride Staining and Its Efficacy on Caries Arrestment in Comparison to Sodium Fluoride With Casein Phosphopeptide-amorphous Calcium Phosphate

University of Baghdad1 site in 1 country60 target enrollmentJanuary 21, 2020

Overview

Phase
Phase 2
Intervention
silver diamine fluoride
Conditions
Dental Caries in Children
Sponsor
University of Baghdad
Enrollment
60
Locations
1
Primary Endpoint
caries arrestment
Status
Suspended
Last Updated
6 years ago

Overview

Brief Summary

This randomized clinical trial aims to compare the effectiveness of two topical fluoride application protocols, namely 38% silver diamine fluoride and sodium fluoride with added casein phosphopeptide-amorphous calcium phosphate (CPP-ACP) in arresting dental caries in children.

Detailed Description

The present randomized clinical study is aiming to evaluate the effectiveness of silver diamine fluoride (SDF) in arresting dentin caries lesions when compared to MI Varnish a 5% sodium fluoride varnish which also contains RECALDENT™\* (CPP-ACP): Casein Phosphopeptide-Amorphous Calcium Phosphate. For this, healthy children aged 4-8 years with at least one active dentin carious lesion will be allocated randomly to one of two treatment groups: Group (1) SDF and Group (2) MI Varnish. Each participant will be assigned to one treatment group to avoid the possible synergistic effect of the different agents. Parents/ guardians of each child will be fully informed regarding the study design, objectives and probable advantages and side effects especially the black discoloration of SDF before their involvement by written consent. The International Caries Detection and Assessment System (ICDAS II) will be used to determine caries diagnosis and activity.visual and tactile examination will be done with a WHO probe to assess the primary outcome. the secondary outcome will be conducted by a questionnaire given to the parents.

Registry
clinicaltrials.gov
Start Date
January 21, 2020
End Date
December 20, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Asmaa Mohammed Khammas

principle investigator

University of Baghdad

Eligibility Criteria

Inclusion Criteria

  • Normal healthy children without any systemic disease ASA 1 physical status.
  • Children with at least one carious dentin lesion in their primary teeth, code 5 (ICDAS II)

Exclusion Criteria

  • Children who suffer from major systemic diseases and require long term medications.
  • Children refuse the study intervention.
  • Children with silver or milk product sensitivity.
  • Presence of any gingival or perioral ulceration or stomatitis.
  • Tooth with abscess, fistula or severe pain.

Arms & Interventions

Group 1: topical application of silver diamine fluoride

38% silver diamine fluoride liquid

Intervention: silver diamine fluoride

Group 2: topical application of MI varnish.

MI Varnish:5% sodium fluoride varnish which also contains RECALDENT™\* (CPP-ACP): Casein Phosphopeptide-Amorphous Calcium Phosphate

Intervention: MI Varnish

Outcomes

Primary Outcomes

caries arrestment

Time Frame: 2 weeks

The measure will be done using international caries detection and assessment system II (ICDAS II) criteria for diagnosing active and arrested caries by WHO probe

Secondary Outcomes

  • Parent perception(0 - 2 weeks)

Study Sites (1)

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