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Effectiveness on SDF Solution and PVP-I Combined NaF Varnish in Preventing Root Caries in Elders

Primary Purpose

Root Caries

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
PVP-I solution combined with NaF varnish
SDF solution
Sponsored by
The University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Root Caries

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • have at least 6 teeth which are not indicated for extraction, and
  • have basic self-care ability.

Exclusion Criteria:

  • have serious debilitating health/medical conditions, and
  • have cognitive problems or major problems in communication.

Sites / Locations

  • The University of Hong Kong

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

PVP-I solution combined with NaF varnish

SDF treated

Arm Description

4-monthly application of 10% povidone-iodine solution and 5% sodium fluoride varnish

Annual application of 38% SDF solution

Outcomes

Primary Outcome Measures

new root caries found in clinical examination
development of new carious lesion on exposed tooth root as assessed in clinical examination where there is a soft decayed root surface on gentle probing with a blunt probe

Secondary Outcome Measures

arrested root caries found in clinical examination
in the follow-up clinical examination, there is arrest of active caries lesions that were present at baseline and found to be a hard root surface upon gentle probing with a blunt probe

Full Information

First Posted
August 29, 2018
Last Updated
September 2, 2018
Sponsor
The University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT03654820
Brief Title
Effectiveness on SDF Solution and PVP-I Combined NaF Varnish in Preventing Root Caries in Elders
Official Title
Effectiveness of Using Silver Diammine Fluoride Solution and Combination of Povidone Iodine and Sodium Fluoride Varnish in Preventing Dental Root Caries in Elders: a Randomized, Double-blind, Non-inferiority Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Unknown status
Study Start Date
August 3, 2017 (Actual)
Primary Completion Date
January 15, 2020 (Anticipated)
Study Completion Date
January 15, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The University of Hong Kong

4. Oversight

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

5. Study Description

Brief Summary
The main objective of this study is to compare the effectiveness and cost-effectiveness of 4-monthly application of 10% povidone iodine solution followed by 5% sodium fluoride varnish with those of annual application of 38% silver diammine fluoride solution on the prevention of new dental root caries in elders. A secondary objective is to compare the effectiveness of the two interventions mentioned above on arresting (halting the progression) active root surface caries in the elders, thus avoiding the need for placing dental restorations. This proposed study is a randomized double-blind controlled clinical trial with 24-month follow-up. A total of 353 elders aged 60 years or above living in residential homes or attending long-term care facilities in different districts in Hong Kong were recruited. Baseline clinical examination will be conducted by two calibrated examiners in the homes using an intra-oral LED light, dental mirrors and probes. Subjects were randomly allocated to one of the two study groups: 1) positive control - received annual application of 38% silver diammine fluoride solution; and 2) test - received application of 10% povidone iodine solution followed by application of 5% sodium fluoride varnish every 4 months. Follow-up examinations will be carried out after 12 and 24 months by the same blinded examiners to assess the clinical outcomes, i.e. whether new dental caries has developed and whether the active root surface caries lesions found at baseline have become arrested (hardened).
Detailed Description
The study population of this proposed clinical trial is adults aged 60 years and above living in residential care homes or attending long-term care facilities in Hong Kong. Totally, 10 residential care homes or long-term care institutions served by NGO dental outreach teams in various districts with different background were selected by the PI in consultation with the NGOs. All elders living in the selected residential homes were invited to attend a free dental examination. Elders fulfilling the inclusion criteria were invited to participate in this study and informed written consent will be obtained before commencement of the study. Dental treatments other than the study interventions were provided by dentists from the NGOs which serve the residential homes. Totally, 353 elder adults enrolled in the trial. The baseline examination was carried out in the residential home by two calibrated examiners, and so will be as follow-up examinations after 12 and 24 months. A portable dental chair, an intra-oral LED light, disposable dental mirrors and CPI probes were used in the examination. For each tooth that was not indicated for extraction, status of its crown and its root were assessed and recorded separately. Caries diagnosis was based on visual and tactile inspection. No radiograph was taken. Plaque and food debris that obscures visual inspection of the tooth surfaces were removed. Four surfaces (mesial, distal, buccal and lingual) per tooth were examined and the status were recorded using the following codes which basically follow the criteria recommended by the International Caries Detection and Assessment System (ICDAS II) Coordinating Committee (2009). The oral hygiene status of the subject was assessed and recorded by using the Visible Plaque Index (Ainamo & Bay, 1975). The presence or absence of visible plaque were recorded on four surfaces (mesial, distal, buccal and lingual) per tooth. The gingival status of the subject was assessed and recorded using the Gingival Bleeding Index (Ainamo & Bay, 1975). The presence or absence of bleeding within 10 seconds after running a probe across the gingival margin was recorded on four surfaces (mesial, distal, buccal and lingual) per tooth. Other information that was recorded included whether the subject normally wears a removable partial denture or not, and the subject's general health status and medications that affect the saliva flow rate. The same calibrated two examiners were blinded by the assignment of the participants. A random sample of 10% of the subjects were re-examined during each examination to monitor intra-examiner reproducibility. At the examinations, the subjects were asked to report on their oral hygiene practices, use of fluoridated toothpaste and other topical fluoride agents, and use of dental services during the study period. Oral health education talk and instructions on how to keep good oral hygiene were provided at baseline and every year to all the elders in the selected residential homes. Standard fluoride toothpastes with 1000-1500 ppm fluoride were provided free to all the elders in the selected residential homes over the 24-month study period. After the baseline examination, subjects satisfying the inclusion criteria of the study were stratified into two groups according to the number of natural teeth with exposed root surfaces in their mouth, those with 12 or fewer teeth and those with 13 or more teeth. The subjects were assigned to one of the two study groups by a research assistant using a block randomization method with a block size of 6. The stratified randomization procedure will help to ensure that the numbers of teeth involved in the two study groups are balanced. The interventions for the two study groups were provided by other dentists and are described below: Group 1 - plaque on the root surfaces of all teeth in the subject's mouth was removed and a 38% SDF solution (Saforide, Toyo Chemical, Japan ) was applied onto the root surfaces using a microbrush/applicator. This will be repeated every year. Group 2 - plaque on the root surfaces of all teeth in the subject's mouth was removed and a 10% povidone iodine solution (Betadine, Mundipharma, Switzerland) was applied, then followed by application of a 5% sodium fluoride varnish (Duraflor, Medicom, Canada) using a microbrush/applicator. This will be repeated every 4 months.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
353 (Actual)

8. Arms, Groups, and Interventions

Arm Title
PVP-I solution combined with NaF varnish
Arm Type
Experimental
Arm Description
4-monthly application of 10% povidone-iodine solution and 5% sodium fluoride varnish
Arm Title
SDF treated
Arm Type
Active Comparator
Arm Description
Annual application of 38% SDF solution
Intervention Type
Device
Intervention Name(s)
PVP-I solution combined with NaF varnish
Intervention Description
4-monthly application of 10% povidone-iodine solution and 5% sodium fluoride varnish
Intervention Type
Device
Intervention Name(s)
SDF solution
Intervention Description
Annual application of 38% SDF solution
Primary Outcome Measure Information:
Title
new root caries found in clinical examination
Description
development of new carious lesion on exposed tooth root as assessed in clinical examination where there is a soft decayed root surface on gentle probing with a blunt probe
Time Frame
24 months
Secondary Outcome Measure Information:
Title
arrested root caries found in clinical examination
Description
in the follow-up clinical examination, there is arrest of active caries lesions that were present at baseline and found to be a hard root surface upon gentle probing with a blunt probe
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: have at least 6 teeth which are not indicated for extraction, and have basic self-care ability. Exclusion Criteria: have serious debilitating health/medical conditions, and have cognitive problems or major problems in communication.
Facility Information:
Facility Name
The University of Hong Kong
City
Hong Kong
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No

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Effectiveness on SDF Solution and PVP-I Combined NaF Varnish in Preventing Root Caries in Elders

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