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Suppression effect on tooth staining evaluated in the newly developed tea beverage/ Randomized controlled trials with double blind crossover study

Suppression effect on tooth staining evaluated in the newly developed tea beverage/ Randomized controlled trials with double blind crossover study - Suppression effect on tooth staining evaluated in the newly developed tea beverage

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000029616
Enrollment
14
Registered
2017-10-18
Start date
2017-10-23
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

None (Healthy adults)

Interventions

Drink the test tea once a day for 3 weeks followed by washout-period, after which drink the placebo tea once a day for 3 weeks. Drink the placebo tea once a day for 3 weeks followed by washout

Sponsors

Tsurumi University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1)Japanese Females aged from 18 to 29, when giving the informed consent. (2)Subjects who never smoke tobacco.

Exclusion criteria

Exclusion criteria: 1. Subjects who are judged as unsuitable for lifestyle questionnaires. 2. Subjects who may have allergy to test foods. 3. Subjects with big covered product or fillings of the front teeth. 4. Subjects who have chronic diseases requiring regular administration, or who have severe diseases. 5. Subjects who have a medical history of serious disease e.g., diabetes, liver disease, kidney disease, and/or heart disease, thyroid gland disease, adrenal gland disease, and/or metabolic disorder. 6. Individuals who have a medical history of diseases affecting digestion and absorption. 7.Subjects who have participated other clinical studies within 1 month of giving the informed consent or who are planning to participate other clinical studies during this study. 8. Subjects who have a medical history of drug. dependence or alcohol dependence. 9. Subjects who are or willing to be pregnant, or who are breast-feeding during this study. 10. Subjects who are planning to have dental work done during this study. 11.Subjects who work in a company developing or manufacturing functional foods. 12. Subjects who are judged as unsuitable by doctor for other reasons.

Design outcomes

Primary

MeasureTime frame
Tooth staining

Countries

Japan

Contacts

Public ContactKaoru Ohmori

Tsurumi University School of Dental Medicine Department of Operative Dentistry

omori-k@tsurumi-u.ac.jp045-580-8427

Outcome results

None listed

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