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A clinical study evaluating the effectiveness of a DARLIE anti-sensitivity toothpaste in relieving dentin hypersensitivity symptoms

Clinical study on the relief of dentin hypersensitivity symptoms by novel phosphorus-calcium toothpaste

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115399
Enrollment
Unknown
Registered
2025-12-25
Start date
2016-03-03
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Dentin hypersensitivity

Interventions

Experimental group:Use the experimental toothpaste every morning and evening, brushing for 2 minutes each time.
Positive control:Use the positive control toothpaste every morning and evening, brushing for 2 minutes each time.
Negative control:Use the negative control toothpaste every morning and evening, brushing for 2 minutes each time.

Sponsors

School & Hospital of Stomatology Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Age between 20 and 55 years old; 2. Good overall health; 3. Symptoms of tooth sensitivity, with at least two teeth (the two sensitive teeth should be in different quadrants and not adjacent) having exposed root dentin. When tested using the Schiff cold air method, at least two teeth must score greater than or equal to 2, with a VAS score greater than or equal to 4, and the tooth sensitivity threshold must be below 20 grams when tested using the Yeaple probe. 4. Must have a daily brushing habit (twice a day, morning and evening).

Exclusion criteria

Exclusion criteria: 1. History of severe oral disease, chronic illness, or allergy to the test product; 2. Progressive periodontal disease or periodontal treatment (including periodontal surgery) within the past year; 3. Mobility of sensitive teeth greater than 1; 4. Extensive dental restorations, suspected pulpitis, caries, enamel cracks, or abutment teeth for removable partial dentures; 5. Taking or currently taking the following medications within one month prior to participation in the study: anticonvulsants, antihistamines, antidepressants, sedatives, tranquilizers, anti-inflammatory agents, and analgesics; 6. Patients with intermittent pain (e.g., lower back pain, arthritis); 7. Participation in a desensitizing toothpaste study within the past 3 months or daily use of other desensitizing toothpastes; 8. Currently participating in other clinical trials; 9. History of allergy to personal care products or toothpaste ingredients; 10. Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Schiff index;

Secondary

MeasureTime frame
Yeaple index;

Countries

China

Contacts

Public ContactBaojun Tai

School & Hospital of Stomatology Wuhan University

duminquan@whu.edu.cn+86 27 8768 6227

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 2, 2026