Effectiveness of SDF With Different Post-treatment Protocols in Arresting Dental Caries

Sponsor
The University of Hong Kong (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05655286
Collaborator
(none)
254
2
24

Study Details

Study Description

Brief Summary

To compare the effectiveness of the semi-annual application of 38% SDF with two post-treatment protocols in arresting dental caries in preschool children

Condition or Disease Intervention/Treatment Phase
  • Drug: 38% SDF treatment
  • Behavioral: not to rinse for at least 30 minutes after SDF treatment
  • Behavioral: rinse mouth immediately after SDF treatment
N/A

Detailed Description

Methods: The randomized double blinded clinical trial will recruit 254 healthy kindergarten children aged 3-5 years old with caries and with parental consent. All the tooth surfaces with carious lesions will receive the semi-annual application of 38% SDF solution. After the treatment, children will be allocated to two groups by an independent research assistant. Two post-treatment protocols are as follows.

Group A - Children are instructed to rinse their teeth with a cup of water containing about 50 ml immediately after SDF treatment. Afterwards, no post-treatment protocol is given to children.

Group B - Children are instructed not to eat and drink for at least 30 minutes. 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 12-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.

Significance: This study will help determine the optimal post-op treatment 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 :
254 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The Effectiveness of Silver Diamine Fluoride Treatment With Different Post-treatment Protocols in Arresting Dental Caries in Primary Teeth of Preschool Children
Anticipated Study Start Date :
Jan 1, 2023
Anticipated Primary Completion Date :
Jun 30, 2024
Anticipated Study Completion Date :
Dec 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group A- immediately rinse mouth

Children are instructed to rinse their teeth with a cup of water containing about 50 ml immediately after SDF treatment. Afterwards, no post-treatment protocol is given to children.

Drug: 38% SDF treatment
Children with active caries will receive 38% silver diamine fluoride treatment

Behavioral: rinse mouth immediately after SDF treatment
After receiving 38% silver diamine fluoride treatment, Children will be asked to rinse their mouths immediately.

Experimental: Group B- not to rinse for at least 30 minutes

Children are instructed not to eat and drink for at least 30 minutes.

Drug: 38% SDF treatment
Children with active caries will receive 38% silver diamine fluoride treatment

Behavioral: not to rinse for at least 30 minutes after SDF treatment
After receiving 38% silver diamine fluoride treatment, Children will be asked not to rinse their mouths for at least 30 minutes.

Outcome Measures

Primary Outcome Measures

  1. Caries status [at 12-month follow-up]

    The proportion of the soft (active) carious tooth lesion surfaces that harden (arrested) at 12 months of follow-up will be measured

Secondary Outcome Measures

  1. The visible plaque index (VPI) [at 12-month 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) the status of visible plaque.

  2. dmft index [at 12-month follow-up]

    The caries experience will be recorded to assess the caries increment by using dmft index at baseline and 12 months later

Eligibility Criteria

Criteria

Ages Eligible for Study:
3 Years to 5 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. 3-5 year old children attending the first to the third year of kindergarten;

  2. free from any systemic conditions and generally healthy;

  3. parents sign informed consent;

  4. having at least 1 tooth with cavitated dentine carious lesion

Exclusion Criteria:
  1. are uncooperative to accept oral examination or treatment;

  2. have a significant systematic disease or long-term medications;

  3. have abnormal dentition.

  4. Teeth having signs or symptoms of irreversible pulpitis and non-vitality will be excluded.

Contacts and Locations

Locations

No locations specified.

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:
NCT05655286
Other Study ID Numbers:
  • HKU20221001
First Posted:
Dec 19, 2022
Last Update Posted:
Dec 19, 2022
Last Verified:
Dec 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
Keywords provided by Chun-Hung Chu, Professor, The University of Hong Kong
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 19, 2022