Effect of Application Time of 38% Silver Diamine Fluoride Solution on Arresting Dental Caries in Preschool Childre

Sponsor
The University of Hong Kong (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04655430
Collaborator
(none)
414
1
9
22.9
18.1

Study Details

Study Description

Brief Summary

To determine the optimal application time of silver diamine fluoride (38% SDF) in arresting dental caries in the primary teeth of preschool children.

Condition or Disease Intervention/Treatment Phase
  • Other: 3-second SDF application
  • Other: 5-second SDF application
  • Other: 10-second SDF application
  • Other: 15-second SDF application
  • Other: 30-second SDF application
  • Other: 45-second SDF application
  • Other: 60-second SDF application
  • Other: 120-second SDF application
  • Other: 180-second SDF application
Phase 2/Phase 3

Detailed Description

Methods: The randomized double blinded clinical trial will recruit 414 healthy kindergarten children aged 3-5 years old with caries and with parental consent. The sample size is sufficient for the appropriate statistical analyses. The children will receive 0.004 mL 38% SDF (typical amount applied per manufacturer's instructions) to treat each caries lesion. The children will be classified into high and low caries rates and equably allocated into nine groups of SDF application time: 3, 5, 15, 30, 45, 60, 120 and 180 seconds. The children will be followed up for 6-months in their kindergartens. Clinical examinations after 6-months will be conducted to assess whether the caries is arrested. Information on confounding factors, such as oral hygiene habits and the use of other fluoride agents, will be collected through a parental questionnaire at the baseline and 6-months follow-up. The examiner, the children and the children's parents will be blind to the treatment allocation. The analysis will determine the significance of differences between the means of arrested caries at the various follow-ups; and Cochran-Armitage test will be used to evaluate the exposure (SDF-application time) to response relationship.

Significance: This study will help determine the optimal application time in SDF treatment. The study provides an evidence-based protocol for the use of silver diamine fluoride to arrest tooth decay in primary teeth of young children.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
414 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Effect of Application Time of 38% Silver Diamine Fluoride Solution on Arresting Dental Caries in Preschool Children: a Randomized Double Blinded Controlled Trial
Anticipated Study Start Date :
Sep 1, 2021
Anticipated Primary Completion Date :
Jan 31, 2023
Anticipated Study Completion Date :
Jul 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: 3-second SDF application

3-second application time of silver diamine fluoride (38% SDF) in arresting dental caries in the primary teeth of preschool children.

Other: 3-second SDF application
Dosage: 3-second 38% SDF solution application

Experimental: 5-second SDF application

5-second application time of silver diamine fluoride (38% SDF) in arresting dental caries in the primary teeth of preschool children.

Other: 5-second SDF application
Dosage: 5-second 38% SDF solution application

Experimental: 10-second SDF application

10-second application time of silver diamine fluoride (38% SDF) in arresting dental caries in the primary teeth of preschool children.

Other: 10-second SDF application
Dosage: 10-second 38% SDF solution application

Experimental: 15-second SDF application

15-second application time of silver diamine fluoride (38% SDF) in arresting dental caries in the primary teeth of preschool children.

Other: 15-second SDF application
Dosage: 15-second 38% SDF solution application

Experimental: 30-second SDF application

30-second application time of silver diamine fluoride (38% SDF) in arresting dental caries in the primary teeth of preschool children.

Other: 30-second SDF application
Dosage: 30-second 38% SDF solution application

Experimental: 45-second SDF application

45-second application time of silver diamine fluoride (38% SDF) in arresting tooth decay (dental caries) in the primary teeth of preschool children.

Other: 45-second SDF application
Dosage: 45-second 38% SDF solution application

Experimental: 60-second SDF application

60-second application time of silver diamine fluoride (38% SDF) in arresting dental caries in the primary teeth of preschool children.

Other: 60-second SDF application
Dosage: 60-second 38% SDF solution application

Experimental: 120-second SDF application

120-second application time of silver diamine fluoride (38% SDF) in arresting dental caries in the primary teeth of preschool children.

Other: 120-second SDF application
Dosage: 120-second 38% SDF solution application

Experimental: 180-second application time

180-second application time of silver diamine fluoride (38% SDF) in arresting dental caries in the primary teeth of preschool children.

Other: 180-second SDF application
Dosage: 180-second 38% SDF solution application

Outcome Measures

Primary Outcome Measures

  1. The visible plaque index (VPI). [at 6-months follow-up]

    Two areas (buccal and lingual) of each of the six index teeth (55/51/63/71/75/83) will be examined and recorded (presence/absence) without visible plaque.

  2. dmft index [at 6-months follow-up]

    The tooth discoloration, tooth status (decayed, missing or filled teeth teeth (dmft) index) and tooth mobility

Eligibility Criteria

Criteria

Ages Eligible for Study:
3 Years to 5 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

(a) 3-5 year old children attending the first to the third year of kindergarten; (b) free from any systemic conditions and generally healthy; (c) parents sign informed consent (d) having at least 1 tooth with cavitated dentine carious lesion.

Exclusion Criteria:
  • uncooperative and difficult to manage, have major systemic diseases such as porphyria, or are on long-term medication such as anti-epileptic drugs.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Local kindergartens Hong Kong Hong Kong

Sponsors and Collaborators

  • The University of Hong Kong

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Chun-Hung Chu, Professor, The University of Hong Kong
ClinicalTrials.gov Identifier:
NCT04655430
Other Study ID Numbers:
  • HKU20201127
First Posted:
Dec 7, 2020
Last Update Posted:
Aug 17, 2021
Last Verified:
Aug 1, 2021
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
Keywords provided by Chun-Hung Chu, Professor, The University of Hong Kong
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 17, 2021