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SDF for the Management of Dental Caries in Children in Primary Dental Care: Protocol for a Feasibility Study

Primary Purpose

Dental Caries in Children

Status
Recruiting
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Silver diamine fluoride
Usual dental care
Sponsored by
Sheffield Teaching Hospitals NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dental Caries in Children

Eligibility Criteria

2 Years - 6 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Children aged 2-6 years Cavitated dentinal caries in any primary tooth No carious involvement of the tooth pulp No dental infection secondary to a non-vital tooth Parent/carer able to complete consent forms (with the support of an interpreter if necessary) Exclusion Criteria: Allergy to any treatment component Caries effecting the pulp Infection secondary to a non-vital tooth Conditions requiring special considerations for the child's dental management where randomisation would not be appropriate for example a medical history including cardiac defects, oncology, hereditary bleeding, or being immunocompromised. Dental anomalies effecting the carious teeth involved: amelogenesis imperfecta, dentinogenesis imperfecta, molar incisor hypomineralisation, abnormal morphology such as double teeth.

Sites / Locations

  • University of SheffieldRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Silver Diamine Fluoride

Usual Care

Arm Description

SDF treatment for caries in the primary teeth of children included

Usual care determined by child's dentist for caries in their primary teeth

Outcomes

Primary Outcome Measures

Data quality of candidate primary outcome measures - ICDAS
• International Caries Detection and Assessment System (ICDAS) - by measuring percentage of completion and data quality
Data quality of candidate primary outcome measure - pain and infection including PUFA
Occurrence or report of pain or infection and Pulpal involvement, Ulceration, Fistula, Abscess (PUFA) index by measuring percentage of completion and data quality
Data quality of candidate secondary outcome measure; referral to secondary care
Referral to secondary care; measuring percentage of completion and data quality
Data quality of candidate secondary outcome measure; Completion course of treatment
Completion course of treatment; measuring percentage of completion and data
Data quality of candidate secondary outcome measure; number of appointments taken for completion of a course of treatment
The number of appointments taken for completion of a course of treatment; measuring percentage of completion and data quality
Data quality of secondary outcome measure; Adherence to intervention protocol or usual care guidelines.
Adherence to intervention protocol or usual care guidelines. ; measuring percentage of completion and data quality
Data quality of candidate secondary outcome measure; Adverse effect(s).
Adverse effect(s). ; measuring percentage of completion and data quality
Data quality of candidate secondary outcome measure; Appointment length
Appointment length; measuring percentage of completion and data quality
Data quality of candidate secondary outcome measure; • number of units of dental activity claimed
Number of units of dental activity claimed; measuring percentage of completion and data quality
Data quality of candidate secondary outcome measure; child and parental/carer reported experience of treatment
Child and parental/carer reported experience of treatment. measuring percentage of completion and data quality
Data quality of candidate secondary outcome measure; Parental/carer reported oral health-related quality of life; P-CPQ16
Parental/carer reported oral health-related quality of life; measuring percentage of completion and data quality
Variability of primary outcome measure; ICDAS or pain and infection
This will be calculated once the specific measure has been chosen based on completion rates and data quality, and discussion with the study panel. Calculation of the variability of the primary outcome measure that is ultimately chosen for a trial should it be deemed feasible.
recruitment, randomisation and retention rates of child participants
Percentage rates of recruitment, randomisation and retention of child participants
recruitment and retention rates of dental professionals
Percentage rates of recruitment and retention of dental professionals
rate of dentists' adherence to the study protocol (treatment allocation)
Percentage of dentists which adhered to the randomisation determined treatment choice for the child
Data quality and percentage completion rates of cost effectiveness data; cost data completed in case report forms by dental professional
Data quality and percentage completion rates of cost effectiveness data; cost data completed in case report forms (time of appointments, treatment carried out, number of UDAs claimed) by dental professional
Data quality of cost effectiveness data; parental questionnaires
Data quality and percentage completion rates of cost effectiveness data; cost questionnaires completed by parents

Secondary Outcome Measures

Full Information

First Posted
June 15, 2023
Last Updated
October 13, 2023
Sponsor
Sheffield Teaching Hospitals NHS Foundation Trust
Collaborators
University of Sheffield, National Institute for Health Research, United Kingdom
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1. Study Identification

Unique Protocol Identification Number
NCT06092151
Brief Title
SDF for the Management of Dental Caries in Children in Primary Dental Care: Protocol for a Feasibility Study
Official Title
A Feasibility Study to Determine Whether a Randomised Controlled Trial of Silver Diamine Fluoride Compared to Usual Care for the Management of Caries in Children's Primary Teeth is Feasible in UK Primary Dental Care
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 22, 2023 (Actual)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
February 28, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sheffield Teaching Hospitals NHS Foundation Trust
Collaborators
University of Sheffield, National Institute for Health Research, United Kingdom

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Dental caries remains a significant health problem in England, effecting 11% of 3-year-olds and 23% of 5-year- olds. Children with dental caries suffer pain, infection and poor oral health-related quality of life. There are different approaches for the management of childhood dental caries but it remains the most common reason for a hospital admission in the UK for children aged 5-9 years, costing the NHS £50 million in 2015-2016. While current approaches have been extensively investigated, their ability to: 1) control pain and infection; 2) prevent hospital admissions, and 3) be implemented within the current NHS contractual arrangements, remains unsatisfactory. Silver diamine fluoride (SDF) is an alternative and non-invasive approach that is applied topically (simple to manage for children) and has proven efficacy in arresting caries progression in primary teeth, principally from studies conducted outside Europe. Its use in primary dental care practice in the UK is limited despite acknowledged need. However, the clinical and cost effectiveness of SDF has not been compared to usual care in the UK, so it is unknown which treatment is more effective. Before a pragmatic randomised controlled trial (RCT) can be conducted into the clinical and cost effectiveness of SDF compared to usual care, there are several uncertainties related to recruitment, retention and fidelity that require investigation in a feasibility study. Research Question Is a randomised controlled trial (RCT) to compare the effectiveness of silver diamine fluoride (SDF) to usual care for the treatment of caries in children's primary teeth feasible in UK primary dental care? Aim The overall aim is to establish whether conducting a RCT to compare SDF to usual care for the treatment of caries in children's primary teeth is feasible. Methods This mixed-method study is a feasibility study with an embedded process evaluation, to compare SDF with usual treatment in primary dental care in the UK. It will be individually randomised, with at least eight dentists, each in a different dental practice and a sample size of 80 participants. There will be ten participants per dentist and equal arm allocation. Follow-up will be for one year. The study will inform whether an RCT is feasible by resolving several key uncertainties. Acceptability and implementation of SDF and the research processes will be explored. Patient and Public Involvement and Engagement (PPIE) representatives will be involved throughout, further informing design including recruitment/retention strategies, participant documentation, analysis, engagement and dissemination.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dental Caries in Children

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
feasibility study
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Silver Diamine Fluoride
Arm Type
Experimental
Arm Description
SDF treatment for caries in the primary teeth of children included
Arm Title
Usual Care
Arm Type
Active Comparator
Arm Description
Usual care determined by child's dentist for caries in their primary teeth
Intervention Type
Device
Intervention Name(s)
Silver diamine fluoride
Intervention Description
silver diamine fluoride - maximum 1 drop to be applied per visit (manufacturer advises this would treat up to 5 teeth)
Intervention Type
Procedure
Intervention Name(s)
Usual dental care
Intervention Description
Usual restorative or preventative care determined by the child's dentist - for examples fillings or crowns
Primary Outcome Measure Information:
Title
Data quality of candidate primary outcome measures - ICDAS
Description
• International Caries Detection and Assessment System (ICDAS) - by measuring percentage of completion and data quality
Time Frame
18 months
Title
Data quality of candidate primary outcome measure - pain and infection including PUFA
Description
Occurrence or report of pain or infection and Pulpal involvement, Ulceration, Fistula, Abscess (PUFA) index by measuring percentage of completion and data quality
Time Frame
18 months
Title
Data quality of candidate secondary outcome measure; referral to secondary care
Description
Referral to secondary care; measuring percentage of completion and data quality
Time Frame
18 months
Title
Data quality of candidate secondary outcome measure; Completion course of treatment
Description
Completion course of treatment; measuring percentage of completion and data
Time Frame
18 months
Title
Data quality of candidate secondary outcome measure; number of appointments taken for completion of a course of treatment
Description
The number of appointments taken for completion of a course of treatment; measuring percentage of completion and data quality
Time Frame
18 months
Title
Data quality of secondary outcome measure; Adherence to intervention protocol or usual care guidelines.
Description
Adherence to intervention protocol or usual care guidelines. ; measuring percentage of completion and data quality
Time Frame
18 months
Title
Data quality of candidate secondary outcome measure; Adverse effect(s).
Description
Adverse effect(s). ; measuring percentage of completion and data quality
Time Frame
18 months
Title
Data quality of candidate secondary outcome measure; Appointment length
Description
Appointment length; measuring percentage of completion and data quality
Time Frame
18 months
Title
Data quality of candidate secondary outcome measure; • number of units of dental activity claimed
Description
Number of units of dental activity claimed; measuring percentage of completion and data quality
Time Frame
18 months
Title
Data quality of candidate secondary outcome measure; child and parental/carer reported experience of treatment
Description
Child and parental/carer reported experience of treatment. measuring percentage of completion and data quality
Time Frame
18 months
Title
Data quality of candidate secondary outcome measure; Parental/carer reported oral health-related quality of life; P-CPQ16
Description
Parental/carer reported oral health-related quality of life; measuring percentage of completion and data quality
Time Frame
18 months
Title
Variability of primary outcome measure; ICDAS or pain and infection
Description
This will be calculated once the specific measure has been chosen based on completion rates and data quality, and discussion with the study panel. Calculation of the variability of the primary outcome measure that is ultimately chosen for a trial should it be deemed feasible.
Time Frame
18 months
Title
recruitment, randomisation and retention rates of child participants
Description
Percentage rates of recruitment, randomisation and retention of child participants
Time Frame
18 months
Title
recruitment and retention rates of dental professionals
Description
Percentage rates of recruitment and retention of dental professionals
Time Frame
18 months
Title
rate of dentists' adherence to the study protocol (treatment allocation)
Description
Percentage of dentists which adhered to the randomisation determined treatment choice for the child
Time Frame
18 months
Title
Data quality and percentage completion rates of cost effectiveness data; cost data completed in case report forms by dental professional
Description
Data quality and percentage completion rates of cost effectiveness data; cost data completed in case report forms (time of appointments, treatment carried out, number of UDAs claimed) by dental professional
Time Frame
18 months
Title
Data quality of cost effectiveness data; parental questionnaires
Description
Data quality and percentage completion rates of cost effectiveness data; cost questionnaires completed by parents
Time Frame
18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Children aged 2-6 years Cavitated dentinal caries in any primary tooth No carious involvement of the tooth pulp No dental infection secondary to a non-vital tooth Parent/carer able to complete consent forms (with the support of an interpreter if necessary) Exclusion Criteria: Allergy to any treatment component Caries effecting the pulp Infection secondary to a non-vital tooth Conditions requiring special considerations for the child's dental management where randomisation would not be appropriate for example a medical history including cardiac defects, oncology, hereditary bleeding, or being immunocompromised. Dental anomalies effecting the carious teeth involved: amelogenesis imperfecta, dentinogenesis imperfecta, molar incisor hypomineralisation, abnormal morphology such as double teeth.
Facility Information:
Facility Name
University of Sheffield
City
Sheffield
ZIP/Postal Code
S102TA
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Miss Timms
Phone
0114 2159310
Email
l.timms@sheffield.ac.uk

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

SDF for the Management of Dental Caries in Children in Primary Dental Care: Protocol for a Feasibility Study

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