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Clinical Trial Study on Toothpaste Containing Stannous Components Inhibiting Dental Plaque

Clinical Trial Study on Toothpaste Containing Stannous Components Inhibiting Dental Plaque

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111733
Enrollment
Unknown
Registered
2025-11-05
Start date
2025-03-08
Completion date
Unknown
Last updated
2025-11-11

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

Conditions

Plaque

Interventions

BAA Series Group:First cycle (5 days) product used: test toothpaste, Brushing method: under staff supervision, use a standardized brushing method to brush only the lingual surfaces of the teeth
Washout period (9 days) product used: control toothpaste, Brushing method: return to personal usual brushing habits, brush the entire mouth
Second cycle (5 days) product used: control toothpaste, Brushing method: under staff supervision, use a standardized brushing method to brush only the lingual surfaces of the teeth
Third cycle (5 days) product used: control toothpaste, Brushing method: under staff supervision, use a standardized brushing method to brush only the lingual surfaces of the teeth.
ABB Series Group:First Cycle (5 days) Product used: control toothpaste, Brushing method: under staff supervision, use a standardized brushing method to brush only the lingual surfaces of the teeth
Washout Period (9 days) Product used: control toothpaste Brushing method: return to personal usual brushing habits, brushing the entire mouth
Second Cycle (5 days) Product used: test toothpaste Brushing method: under staff supervision, use a standardized brushing method to brush only the lingual surfaces of the teeth
Washout Period (9 days) Product used: control toothpaste, Brushing method: return to personal usual brushing habits, brushing the entire mouth
Third Cycle (5 days) Product used: test toothpaste, Brushing method: under staff supervision, use a standardized brushing method to brush only the lingual surfaces of the teeth.

Sponsors

Peking University School of Stomatology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Overall good health, with more than 20 teeth available for examination (including at least four molars, excluding third molars); 2. Age between 19 and 70 years; women must not be pregnant or breastfeeding; 3. Possess an appropriate level of plaque (PLI >= 1.5); 4. Not participating in other similar clinical studies at the same time; 5. Signed informed consent and able to complete the clinical trial as required.

Exclusion criteria

Exclusion criteria: 1. History of allergy to the ingredients of the test toothpaste; 2. Currently taking or using medications that may affect the test results; 3. Use of antibiotics within one month prior to participating in the study; 4. Suffering from moderate to severe periodontitis; 5. Having more than two open caries or oral mucosal lesions; 6. Women who are pregnant, breastfeeding, or planning to become pregnant during the study period; 7. Presence of crowns, implants, orthodontic appliances, wearing removable partial dentures or orthodontic retainers in the mouth; 8. Smokers or those with a recent history of smoking, including e-cigarettes; 9. Having systemic diseases (such as blood disorders, liver diseases, diabetes, etc.).

Design outcomes

Primary

MeasureTime frame
Turesky-modified Quigley-Hein Plaque Index;

Countries

China

Contacts

Public ContactLiu Xuenan; Zhou Shuangying

Peking University School of Stomatology

shyingzhou@126.com+86 186 1831 1068

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026