Functional Validation of Lactobacillus Containing Oral Tablet
Primary Purpose
Periodontal Disease
Status
Completed
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
troches
Sponsored by
About this trial
This is an interventional prevention trial for Periodontal Disease focused on measuring Caries, Periodontal disease
Eligibility Criteria
Inclusion Criteria:
- 20~65 years old
- At least 20 teeth except wisdom teeth
Exclusion Criteria:
- Smoking habits
- Oral cancer or other serious oral diseases.
- Pregnancy
- Severe chronic diseases
- Coagulation diseases
- Long-term or regular use of medication (anti-epileptics, antihistamines, anti-inflammatory, sedatives, tranquilizers, analgesics, Chinese herbs)
- Allergy to test products
Sites / Locations
- National Cheng Kung University Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Troches
Troches do not contain probiotics
Arm Description
25 persons take one probiotic troche after each meal.
25 persons take one troche that does not contain probiotics after each meal.
Outcomes
Primary Outcome Measures
Periodontal pocket depth
The probe should be walked around each tooth, and the probing depth of each tooth will be recorded in its six aspect (MB, M, DB, ML, L, DL)
Secondary Outcome Measures
Gingival index
The scores from the six areas of the tooth may be added and divided by six to give the GI for the tooth.
By adding the indices for the teeth and dividing by the total number of teeth examined, the Gl for the individual is obtained.
Plaque index
The disclosing solution is painted on all exposed tooth surfaces. After the patient has rinsed, the operator, using an explorer or the tip of a probe, examines each stained surface for soft accumulations at the dentogingival junction. When found, they are recorded by making a dash in the appropriate spaces on the record form.Silmilar to the gingival index, each of the six gingival areas of the tooth will be examined and recorded.
The overall plaque index is calculated by dividing the number of plaque containing surfaces with the total number of available surfaces.
Plaque microorganisms
The ratio of Firmicutes/ Bacteroidetes/Streptococcus mutans/Porphyromonas gigivalis, as well as total count of microorganisms from the plaque collected.
Full Information
NCT ID
NCT04873505
First Posted
April 22, 2021
Last Updated
May 30, 2023
Sponsor
National Cheng-Kung University Hospital
Collaborators
Grape King Bio Ltd.
1. Study Identification
Unique Protocol Identification Number
NCT04873505
Brief Title
Functional Validation of Lactobacillus Containing Oral Tablet
Official Title
Functional Validation of Lactobacillus Containing Oral Tablet
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
October 30, 2020 (Actual)
Primary Completion Date
January 29, 2022 (Actual)
Study Completion Date
April 29, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Cheng-Kung University Hospital
Collaborators
Grape King Bio Ltd.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Dental caries and periodontal disease are the two most common diseases in dentistry. Caries was caused by the acidic environment produced through the interaction of oral flora (biofilm) and fermentable food residues on the tooth surface over time thus to destroying the tooth structure. Periodontal disease was also highly associated with microorganisms in the periodontal tissues and the inflammatory response of the host that irritate and destruct periodontal and bone tissues. Recent studies have found that both stress and eating habits are associated with decline in oral health. Probiotics have been traditionally used for prevention and treatment of gastrointestinal diseases. In the past decade, accumulated studies further indicate that imbalance of oral microflora is highly related to oral diseases thus probiotics has been suggested for maintaining oral health. It is thus conceivable that probiotics as a buccal tablet may potentially restore the balance of oral flora providing a novel strategy to combat oral diseases. Such strategy may also harbor great opportunities for the long-term management of dental caries and periodontal infections. In order to evaluate the efficacy of probiotics buccal tablet in rebalancing oral flora and control to reduce the incidence of dental caries and periodontal diseases, the investigators aimed to conduct a comprehensive clinical trials for subsequent product optimization.
Grape King Biotechnology Co., Ltd. has successfully developed oral tablet mainly composed of Lactobacillus plantarum GKD7 and Pediococcus acidilactici GKA4. These two probiotics were found to inhibit caries through producing protective biofilms thus are more effective than commercially available anti-tooth decay products. To evaluate the future potential of clinical applications of the related products series and the impact on oral health-related indicators, the investigators will explore the changes in the the following disease associated indexes before and after using the oral tablet. These include periodontal pocket depth, the gingival inflammation index, the plaque index, and the ratio of Firmicutes, Bacteroidetes, Streptococcus mutans, and Porphyromonas gigivalis, as well as quantification of total bacteria. This clinical study will be performed in Department of Stomatology in NCKUH in collaboration with periodontics session and Family Dentistry session. A total of 50 healthy individuals within the range of 20~65 years old will be enrolled.
Detailed Description
The following parameters will be collected and analyzed: periodontal pocket depth, the gingival inflammation index, the plaque index, and the ratio of Firmicutes/ Bacteroidetes/Streptococcus mutans/Porphyromonas gigivalis, as well as total count of microorganisms from the plaque collected.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Periodontal Disease
Keywords
Caries, Periodontal disease
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Troches
Arm Type
Experimental
Arm Description
25 persons take one probiotic troche after each meal.
Arm Title
Troches do not contain probiotics
Arm Type
Placebo Comparator
Arm Description
25 persons take one troche that does not contain probiotics after each meal.
Intervention Type
Dietary Supplement
Intervention Name(s)
troches
Intervention Description
Take one troche after each meal.
Primary Outcome Measure Information:
Title
Periodontal pocket depth
Description
The probe should be walked around each tooth, and the probing depth of each tooth will be recorded in its six aspect (MB, M, DB, ML, L, DL)
Time Frame
1 hour
Secondary Outcome Measure Information:
Title
Gingival index
Description
The scores from the six areas of the tooth may be added and divided by six to give the GI for the tooth.
By adding the indices for the teeth and dividing by the total number of teeth examined, the Gl for the individual is obtained.
Time Frame
30 minutes
Title
Plaque index
Description
The disclosing solution is painted on all exposed tooth surfaces. After the patient has rinsed, the operator, using an explorer or the tip of a probe, examines each stained surface for soft accumulations at the dentogingival junction. When found, they are recorded by making a dash in the appropriate spaces on the record form.Silmilar to the gingival index, each of the six gingival areas of the tooth will be examined and recorded.
The overall plaque index is calculated by dividing the number of plaque containing surfaces with the total number of available surfaces.
Time Frame
1 hour
Title
Plaque microorganisms
Description
The ratio of Firmicutes/ Bacteroidetes/Streptococcus mutans/Porphyromonas gigivalis, as well as total count of microorganisms from the plaque collected.
Time Frame
30 minutes
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
20~65 years old
At least 20 teeth except wisdom teeth
Exclusion Criteria:
Smoking habits
Oral cancer or other serious oral diseases.
Pregnancy
Severe chronic diseases
Coagulation diseases
Long-term or regular use of medication (anti-epileptics, antihistamines, anti-inflammatory, sedatives, tranquilizers, analgesics, Chinese herbs)
Allergy to test products
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ying-Ying Chang
Organizational Affiliation
National Cheng-Kung University Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
National Cheng Kung University Hospital
City
Tainan
Country
Taiwan
12. IPD Sharing Statement
Plan to Share IPD
No
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Functional Validation of Lactobacillus Containing Oral Tablet
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