Silver Diamine Fluoride and Gingivitis in Geriatric Patients
Primary Purpose
Gingivitis
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Silver Diamine Fluoride
Normal Saline
Sponsored by
About this trial
This is an interventional treatment trial for Gingivitis focused on measuring Gingivitis and geriatric patients, Silver Diamine Fluoride and gingivitis, Sliver Diamine Fluoride
Eligibility Criteria
Inclusion Criteria:
- Age group 65 years and older
- Males and females
- Minimum of 6 remaining teeth with gingivitis (at least one posterior tooth should be present)
- Every participant should agree to not brush or floss three days prior the data collection
- Every participant should agree to not use any mouthwash or Fluoride treatment for the entire study period
- All socioeconomic status included
Exclusion Criteria:
- Active chemotherapy or radiotherapy
- Known history of allergy to Silver Particles
- Uncontrolled diabetes
- Use of antibiotics in the last three months
- Periodontal therapy in the last 3 months
- Mouth rinse such as Chlorhexidine (CHX) at least 30 days prior to the study
- Smoking
- Epileptic patients on medication cause gingival overgrowth
- Patients who are unable to give consent
- Teeth with periodontitis
Sites / Locations
- Notre Dame Court (Seniors Independent Living)
- Dickinson Place (Seniors Independent Living)
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Silver Diamine Fluordie Application
Normal Saline
Arm Description
This group will receive Silver Diamine Fluoride (SDF) application once every week within three weeks period
This control group will receive normal saline application once a week within a a three-week period
Outcomes
Primary Outcome Measures
The change in Gingival Index GI (for Gingival Inflammation)
The change in Gingival Index GI (for Gingival Inflammation) from Baseline before the application of either Silver Diamine Fluoride or Chlorhexidine and at two weeks and four weeks after the final application of either Silver Diamine Fluoride or Chlorhexidine
The change in Plaque Index PI (for dental plaque accumulation)
The change in Plaque Index PI (for dental plaque accumulation) from baseline before the application of either Silver Diamine Fluoride or Chlorhexidine and at two weeks and four weeks after the final application of either Silver Diamine Fluoride or Chlorhexidine
Secondary Outcome Measures
Assessment of microbial counts in Dental Plaque
Dental Plaque sample taken from each participant, labeled and send to the lab for analysis of bacterial counts (using Ubiome dental kit)
Full Information
NCT ID
NCT03445286
First Posted
February 13, 2018
Last Updated
October 5, 2020
Sponsor
Texas A & M University Baylor College Of Dentistry
1. Study Identification
Unique Protocol Identification Number
NCT03445286
Brief Title
Silver Diamine Fluoride and Gingivitis in Geriatric Patients
Official Title
Effect of Silver Diamine Fluoride on the Treatment of Gingivitis in Geriatric Patients
Study Type
Interventional
2. Study Status
Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
January 29, 2019 (Actual)
Primary Completion Date
January 10, 2020 (Actual)
Study Completion Date
May 22, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Texas A & M University Baylor College Of Dentistry
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
Gingivitis in the geriatric population is one of the growing global public health concerns, thus finding the most effective and non-invasive approach to prevent and treat gingivitis in the geriatric population is essential to prevent tooth loss and maintain oral health and function. Silver Diamine Fluoride (SDF) is Class II medical device. It was cleared for use in US August 2014 and became commercially available in April 2015. It is a chemical agent which has bifunctional properties. The silver itself kills caries causing bacteria directly. Silver and fluoride together interact to form fluorapatite, in addition, assist in hardening the teeth and preventing further demineralization.
Even though SDF has been approved in dental caries prevention and treatment, there are no published studies or evidence that evaluated the direct effect of SDF on gingivitis. If SDF improves or prevents gingivitis is unknown. The main goal of this clinical study is to investigate the effect of SDF on gingival status in geriatric patients with gingivitis. There is an urgent need to solve this common oral disease in the geriatric population. The logic for this research in a geriatric population is to find the most effective approach to treat gingivitis to prevent tooth loss and maintain oral health and function.
To find an effective approach to treat gingivitis in the geriatric group, we will investigate the effectiveness of SDF application on gingival tissues in this group. The patients with gingivitis will be randomly allocated to two groups: group1(case group) will receive SDF application and group 2 (control group) will receive a normal saline application. The gingiva will be evaluated for both groups at baseline before the application. Then 2 weeks and 4 weeks after the last application of the intervention. In addition, a sample of plaque will be taken from the teeth selected in this study by swab using the dental kit (Ubiome) before and after both applications to quantify the presence of bacterial pathogen at baseline and follow up visits. The feasibility of this proposed therapy is supported by published literature that has shown that SDF was effective in dental and root caries prevention and treatment in geriatric patients.
Detailed Description
The Aims
Aim 1 To investigate the effect of SDF application on gingival status in elder patients with gingivitis. To accomplish this aim, the subjects with gingivitis will be randomly allocated to two groups: group 1(case group) will receive SDF application and group 2 (control group) will receive Normal Saline. The SDF and normal saline will apply on the selected teeth with gingivitis once a week during a three-week period. The gingival status will be evaluated at baseline before the application of either SDF or normal saline. Then at the second week and fourth week after the final application. The measurable outcomes will be Plaque Index (PI) and the Gingival Index (GI). In addition, record of existing brushing and flossing habits. If SDF application shows an improvement in the gingival condition (reduction in the plaque and gingival indices) in treatment group comparing to the control group it indicates that its effectiveness not only on dental caries as published, but it is also may extended to include gingivitis.
Aim 2 To quantify the presence of bacterial pathogen in the dental biofilm. To accomplish this aim, a sample of dental plaque will be taken from the teeth selected in this study by swab using the dental kit (Ubiome) before and after the SDF or normal saline application to quantify the presence of bacterial pathogen at baseline before the application, 2 weeks and 4 weeks after the application.
Summary:
The proposed therapeutic intervention of Silver Diamine Fluoride (SDF) in treating geriatric patients with gingivitis will establish a new adjunctive and inexpensive protocol for treatment of gingivitis. Gingivitis is inflammation of gingival tissues caused by dental biofilm bacterial infection. Left untreated, gingivitis will cause tooth loss. The preliminary results will provide new recommendations for treating geriatric patients in a safe, effective, and low-cost manner. This study will also address the gap in scientific knowledge regarding the use of SDF to treat gingivitis in elderly patients.
Research Hypothesis: The application of SDF varnish is expected to improve the gingival condition and can be an effective approach in the treatment of gingivitis in geriatric patients.
Null Hypothesis: The application of SDF varnish does not improve the gingival condition and cannot be an effective approach in the treatment of gingivitis in geriatric patients.
Research Question: Does the application of silver Diamine Fluoride on teeth with gingivitis will improve the gingival condition in geriatric patients with gingivitis
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gingivitis
Keywords
Gingivitis and geriatric patients, Silver Diamine Fluoride and gingivitis, Sliver Diamine Fluoride
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The participants with gingivitis are randomly allocated to two groups: group 1(case group) who will receive SDF application once every week within three weeks period and group 2 (control group) who will receive normal saline application once a week within three-week period
Masking
ParticipantOutcomes Assessor
Masking Description
The participants and outcome Assessor will be blinded The participants will be blinded about which interventions they will receive and the Outcomes Assessor who will evaluate the gingival condition will be blinded about the interventions, and also the care provider who will apply the intervention will be blinded
Allocation
Randomized
Enrollment
48 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Silver Diamine Fluordie Application
Arm Type
Experimental
Arm Description
This group will receive Silver Diamine Fluoride (SDF) application once every week within three weeks period
Arm Title
Normal Saline
Arm Type
Placebo Comparator
Arm Description
This control group will receive normal saline application once a week within a a three-week period
Intervention Type
Device
Intervention Name(s)
Silver Diamine Fluoride
Other Intervention Name(s)
Advantage Arrest
Intervention Description
Silver Diamine Fluoride (Advantage Arrest) for the experimental group
Intervention Type
Other
Intervention Name(s)
Normal Saline
Intervention Description
Normal Saline for the control group
Primary Outcome Measure Information:
Title
The change in Gingival Index GI (for Gingival Inflammation)
Description
The change in Gingival Index GI (for Gingival Inflammation) from Baseline before the application of either Silver Diamine Fluoride or Chlorhexidine and at two weeks and four weeks after the final application of either Silver Diamine Fluoride or Chlorhexidine
Time Frame
Assessment of the change from the baseline at 2 weeks and 4 weeks after the final application of either Silver Diamine Fluoride or Chlorhexidine
Title
The change in Plaque Index PI (for dental plaque accumulation)
Description
The change in Plaque Index PI (for dental plaque accumulation) from baseline before the application of either Silver Diamine Fluoride or Chlorhexidine and at two weeks and four weeks after the final application of either Silver Diamine Fluoride or Chlorhexidine
Time Frame
Assessment of the change from the baseline at 2 weeks and 4 weeks after the final application of either Silver Diamine Fluoride or Chlorhexidine
Secondary Outcome Measure Information:
Title
Assessment of microbial counts in Dental Plaque
Description
Dental Plaque sample taken from each participant, labeled and send to the lab for analysis of bacterial counts (using Ubiome dental kit)
Time Frame
Three times evaluation at baseline before the application of the intervention, then at 2 weeks and 4 weeks after the final application of either Silver Diamine Fluoride or Chlorhexidine
10. Eligibility
Sex
All
Minimum Age & Unit of Time
65 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Age group 65 years and older
Males and females
Minimum of 6 remaining teeth with gingivitis (at least one posterior tooth should be present)
Every participant should agree to not brush or floss three days prior the data collection
Every participant should agree to not use any mouthwash or Fluoride treatment for the entire study period
All socioeconomic status included
Exclusion Criteria:
Active chemotherapy or radiotherapy
Known history of allergy to Silver Particles
Uncontrolled diabetes
Use of antibiotics in the last three months
Periodontal therapy in the last 3 months
Mouth rinse such as Chlorhexidine (CHX) at least 30 days prior to the study
Smoking
Epileptic patients on medication cause gingival overgrowth
Patients who are unable to give consent
Teeth with periodontitis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
WEDAD ALSHEHRI, BSDH, MS.
Organizational Affiliation
Texas A&M University College of Dentistry
Official's Role
Study Director
Facility Information:
Facility Name
Notre Dame Court (Seniors Independent Living)
City
Dallas
State/Province
Texas
ZIP/Postal Code
75208
Country
United States
Facility Name
Dickinson Place (Seniors Independent Living)
City
Dallas
State/Province
Texas
ZIP/Postal Code
75246
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Silver Diamine Fluoride and Gingivitis in Geriatric Patients
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