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A study to verify the halitosis improvement and oral rinsing effects

A study to verify the halitosis improvement and oral rinsing effects: an open-label trial - A study to verify the halitosis improvement and oral rinsing effects

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000049663
Enrollment
10
Registered
2022-12-01
Start date
2022-12-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Healthy Japanese subjects

Interventions

Duration: Four weeks Test product: Mouthwash (containing 0.005% hypochlorous acid) Administration: On the day of screening (before using test product
Scr), after each pre-use measurement, rinse your mouth with approximately 20 ml of test product for approximately 20 seconds and spit it out. After that, receive each measurement again. After the sta

Sponsors

ORTHOMEDICO Inc.
Lead Sponsor
Medical Corporation Seishinkai, Takara Clinic Nerima Medical Association, Minami-machi Clinic Medical Corporation Yuseikai, Horiuchi Dental Clinic
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Japanese 2. Men or women 3. Adults 4. Healthy subjects 5. Subjects who are concerned about their halitosis 6. Subjects will be selected based on the results of halitosis measurement at Scr

Exclusion criteria

Exclusion criteria: Subjects who 1. are undergoing medical treatment or have a medical history of malignant tumor, heart failure, and myocardial infarction 2. have a pacemaker or an implantable cardioverter defibrillator (ICD) 3. are currently undergoing treatment for any of the following chronic diseases: cardiac arrhythmia, liver disorder, kidney disorder, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension, or any other chronic diseases 4. use or take "Foods for Specified Health Uses," or "Foods with Functional Claims" in daily 5. are currently taking medications (including herbal medicines) and supplements 6. are allergic to medicines and/or the test food related products 7. show allergic reactions to hypochlorous acid 8. are pregnant, lactating, or planning to become pregnant during this trial 9. suffer from COVID-19 10. have been enrolled in other clinical trials within the last 28 days before the agreement to participate in this trial or plan to participate another trial during this trial 11. are judged as ineligible to participate in this study by the physician 12. take functional food/beverage to improve halitosis 13. use artificial tooth, post crowns, dentures, implants or bridges 14. regularly use gargle medicine, medicated toothpaste, floss, interdental brush, and mouthwash 15. have a medical history or current history of Sjogren's syndrome, or who are suspected it 16. have diseases associated with salivary gland such as dry mouse and salivary stone disease 17. are undergoing medical treatment for periodontosis or dental caries 18. are dental treatment or have dental diseases 19. are smokers, or started smoking cessation within one year before the agreement to participate in this trial 20. plan to receive dental maintenance care (such as removing dental plaque) at the dental clinic during this trial 21. are more likely to get stomatitis 22. cannot brush their teeth three times a day

Design outcomes

Primary

MeasureTime frame
1. B/B value

Secondary

MeasureTime frame
1. Amount of adenosine triphosphate (ATP) in saliva

Countries

Japan

Contacts

Public ContactNaoko Suzuki

ORTHOMEDICO Inc. R&D Department

nao@orthomedico.jp03-3818-0610

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026