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Recruiting NCT07628712

Dentine Hypersensitivity Using Dentine Adhesive With Strontium-doped Bioactive Glass-Ceramic

Conditions: Dentine Hypersensitivity

Sex: All
Ages: 18 Years – 69 Years
Healthy volunteers: No
Phase: NA
Enrollment: 142
Sponsor: The University of Hong Kong

Location: Clinical Research Center, the Prince Philips Dental Hospital Hong Kong

Summary

The goal of this clinical trial is to determine whether strontium-doped bioactive glass-ceramic (SBGC)-filled dentine adhesive is effective in relieving dentine hypersensitivity. The main question it aims to answer is: Is SBGC-filled dentine adhesive more effective in reducing dentine hypersensitivity than non-SBGC-filled dentine adhesive? Researchers will compare SBGC-filled dentine adhesive to a dentine adhesive to see if SBGC-filled dentine adhesive is more effective at relieving dentine hypersensitivity. Participants will receive a single application of either SBGC-filled dentine adhesive (intervention group) or dentine adhesive (control group) on the root surfaces of teeth presenting with pain subject to an air-blast test. The degree of pain will be assessed using a Sensitivity Score at baseline, immediately after application of either the intervention dentine adhesive or control dentine adhesive. The participants will visit the clinic at 1 month, 3 months and 6 months for re-assessment of the severity of dentine hypersensitivity.

Eligibility Criteria

Inclusion Criteria: * individuals who experienced cervical dentine sensitivity for 1 month or more Exclusion Criteria: * 1\) \

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07628712). StuddyBuddy aggregates publicly available trial information.