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Clinical Observational Trial on the Efficacy of Jun Xiao Bai Toothpaste Containing Mesoporous Nano-Hydroxyapatite with a Purity of 99%+ in Reducing Dentin Hypersensitivity

Clinical Observational Trial on the Efficacy of Jun Xiao Bai Toothpaste Containing Mesoporous Nano-Hydroxyapatite with a Purity of 99%+ in Reducing Dentin Hypersensitivity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094579
Enrollment
Unknown
Registered
2024-12-25
Start date
2025-02-05
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Dentin Hypersensitivity

Interventions

Test group:Jun Xiao Bai Toothpaste Containing Mesoporous Nano-Hydroxyapatite with a Purity of 99%+
Control group:Baiyu Toothpaste

Sponsors

West China Hospital of Stomatology, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. The whole body is in good health and can participate in the examination at any time during the trial; 2. Age between 18-65 years, both genders are acceptable; 3. Good compliance with check-ups during the trial period, able to follow health guidance, and capable of completing follow-up visits effectively; 4. At least 2 teeth with dentin hypersensitivity, with a Schiff Cold Air Sensitivity Score for cold air stimulation >=2; and a Visual Analogue Scale (VAS) score for cold air stimulation >=30 mm; 5. Women must not be in pregnancy or lactation; 6. No allergies to toothpaste or its ingredients; 7. No use of the following medications in the month before participating in the study: anticonvulsants, antihistamines, antidepressants, sedatives, anxiolytics; 8. Not currently using anti-dentin hypersensitivity toothpaste; not concurrently participating in other similar experimental studies; 9. Only people with continuous or more severe dentin hypersensitivity symptoms during the washout period are included as participants.

Exclusion criteria

Exclusion criteria: 1. The participant has acute pulpitis or apical periodontitis, oral mucosal chronic diseases such as lichen planus, leukoplakia, pemphigus, etc.; has chronic systemic diseases that cause intermittent or persistent pain, such as arthritis; or has a history of allergy to the test product; 2. The patient has received periodontal treatment (including periodontal surgery) within the past 6 months; 3. The mobility of sensitive teeth is greater than Grade I; sensitive teeth have moderate or deep caries, large fillings or crowns, obvious cracks in the enamel, or teeth with full crowns, abutment teeth for fixed or removable partial dentures; 4. The symptoms of dentin hypersensitivity are related to gum pain caused by occlusal trauma, heat, or chemical burns; diseases in other parts of the body are the cause of dentin hypersensitivity; 5. Has undergone dental treatment for tooth sensitivity in the past; teeth whitening within the past 8 weeks; use of over-the-counter professional anti-dentin hypersensitivity toothpaste within the past 3 months; 6. Has a history of needing long-term use of anti-inflammatory drugs, regular analgesics, anticonvulsants, antihistamines, antidepressants, sedatives, and other psychotropic medications; has diseases related to eating disorders and vomiting; 7. Women who are pregnant or breastfeeding; 8. Smokers; 9. Subjects deemed ineligible for enrollment by the investigator.

Design outcomes

Primary

MeasureTime frame
Schiff Cold Air Sensitivity Scale;

Secondary

MeasureTime frame
Visual Analogue Scale for Pain;Side Effects;

Countries

China

Contacts

Public ContactZhao Lei

West China Hospital of Stomatology Sichuan University

jollyzldoc@163.com+86 135 5103 2465

Outcome results

None listed

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