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Comparative analysis of oral and intestinal environment in healthy subject and patients with oral disease.

Comparative analysis of oral and intestinal environment in healthy subject and patients with oral disease. - Comparative analysis of oral and intestinal environment in healthy subject and patients with oral disease.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000031334
Enrollment
150
Registered
2018-02-16
Start date
2018-02-17
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Men and women

Interventions

None listed

Sponsors

Hiyoshi Oral Health Clinics
Lead Sponsor
Lion Corporation
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (A-1) Males and females aged 20 to 65 years old. (A-2) Subjects who don't regularly use specific medicines. (A-3) Subjects who show understanding of the study procedures and agreement with participating the study by written informed consent prior to the study. (B-1) Males and females aged 20 to 79 years old. (B-2) Subjects who are found carious pit that are required therapy in adult tooth by visual or X-ray. (B-3) Subjects who show understanding of the study procedures and agreement with participating the study by written informed consent prior to the study. (C-1) Males and females aged 20 to 79 years old. (C-2) Subjects who have at least 1 periodontal pockets that are 4 mm or deeper with bleeding. (C-3) Subjects who do not have carious pit. (C-4) Subjects who show understanding of the study procedures and agreement with participating the study by written informed consent prior to the study. (D-1) Males and females aged 20 to 79 years old. (D-2) Subjects who do not have periodontal pockets that are 4 mm or deeper. (D-3) Subjects who have 10% or less bleeding tooth surface. (D-4) Subjects who do not have carious pit. (D-5) Subjects who show understanding of the study procedures and agreement with participating the study by written informed consent prior to the study. (E-1) Males and females aged 80 to 100 years old. (E-2) Subjects who have 26 or greater original teeth. (E-3) Subjects who did not receive treatment of carious or periodontal disease during last 10 years. (E-4) Subjects who show understanding of the study procedures and agreement with participating the study by written informed consent prior to the study.

Exclusion criteria

Exclusion criteria: (A-1) Subjects who have denture or implants. (A-2) Smoker (A-3) Subjects who consumed antibiotics during last 6 months. (A-4) Subjects who did mouth cleaning, eating, or drinking except water during last 1 hour. (A-5) Subjects who did mouth cleaning from last night to sampling. (A-6) Subjects who is pregnant. (A-7) Subjects who have been determined ineligible by principal investigator. (B-1) Subjects who have denture or implants. (B-2) Smoker (B-3) Subjects who consumed antibiotics during last 6 months. (B-4) Subjects who is in orthodontic treatment. (B-5) Subjects who did mouth cleaning, eating, or drinking except water during last 1 hour. (B-6) Subjects who is pregnant. (B-7) Subjects who have been determined ineligible by principal investigator. (C-1) Subjects who have denture or implants. (C-2) Smoker (C-3) Subjects who consumed antibiotics during last 6 months. (C-4) Subjects who is in orthodontic treatment. (C-5) Subjects who did mouth cleaning, eating, or drinking except water during last 1 hour. (C-6) Subjects who is pregnant. (C-7) Subjects who have been determined ineligible by principal investigator. (D-1) Subjects who have denture or implants. (D-2) Smoker (D-3) Subjects who consumed antibiotics during last 6 months. (D-4) Subjects who is in orthodontic treatment. (D-5) Subjects who did mouth cleaning, eating, or drinking except water during last 1 hour. (D-6) Subjects who is pregnant. (D-7) Subjects who have been determined ineligible by principal investigator. (E-1) Subjects who did mouth cleaning, eating, or drinking except water during last 1 hour. (E-2) Subjects who have been determined ineligible by principal investigator.

Design outcomes

Primary

MeasureTime frame
16S rRNA gene-based metagenome analysis and metabolome analysis of oral cavity samples

Secondary

MeasureTime frame
* 16S rRNA gene-based metagenome analysis and metabolome analysis of fecal samples * Background research * Questionnaire

Countries

Japan

Contacts

Public ContactShinnosuke Murakami

Metabologenomics, Inc. Headquarters

clinical-trials@metagen.co.jp+81-235-64-0330

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026