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Crossover test for reducing oral malodor by the chewing gums containing Myrsine seguinii extracts

Crossover test for reducing oral malodor by the chewing gums containing Myrsine seguinii extracts - Oral malodor reducing effect by Myrsine seguninii chewing gum

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000023832
Enrollment
20
Registered
2016-08-31
Start date
2015-12-31
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

Physiological halitosis

Interventions

High-dose extract-containing Chewing gum Middle-dose extract-containing Chewing gum Low-dose extract-containing Chewing gum Control Chewing gum

Sponsors

Lotte Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: A. Normally eating three times daily. B. In the screening test, 1.5 ng or more than 1.5 ng of hydrogen sulfide in 10 mL mouth air by gas chromatography. C. No dental treatment now and at least 20 natural teeth. D. Without the habit to brush the tongue during toothbrushing (It was allowed who quitted the tongue brushing during the test period) E. Received the sufficient explanation about the purpose and the content of the study, had the consent ability, volunteered to voluntarily participate in to fully understand, and agreed to the study participation in writing

Exclusion criteria

Exclusion criteria: 1. Smokers 2. Suffering from diabetes mellitus, Chronic nephritis, stomach disorders, lung diseases, malignant tumors, hepatitis, taking medicines. 3. Utilizing mouthwash or anti-malodor products daily. 4. Currently participating or trying to participate in the studies of other medicines or foods. 5. At the screening test, being diagnosed with periodontitis or dental caries. 6. Wearing removable denture. 7. Taking antibiotics / antimicrobial within one month before the screening test. 8. With food allergies, lactose intolerance or feeling of unwellness by the dairy products. 9. Pregnant or with the intention of pregnancy or while breast-feeding during the test. 10. Judged to be inappropriate to the test by the chief researcher because of the other reasons than mentioned above.

Design outcomes

Primary

MeasureTime frame
The concentration of Volatile Sulfur Compounds (hydrogen sulfide and methyl mercaptan) in the oral air

Countries

Japan

Contacts

Public ContactKeishirou Yoshida

LOTTE CO., LTD. Central Laboratory, Food Function Development Section

yoshida_keishirou@lotte.co.jp048-837-0187

Outcome results

None listed

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