Evaluation of Different Non-Invasive Methods in the Treatment of Dentin Hypersensitivity Associated With Non-Carious Cervical Lesions: A Split-Mouth Clinical Study
Starting soon · Not applicable
Conditions studied: Non-Carious Cervical Lesions (NCCLs), Dentin Hypersensitivity
In brief
The aim of this split-mouth clinical study is to compare the effectiveness of D Blue diode laser application and ProSylc bioactive glass powder application in reducing dentin hypersensitivity in patients with non-carious cervical lesions (NCCLs). Different treatment modalities will be applied within the same participant, and changes in dentin hypersensitivity will be evaluated following treatment. The primary outcome measure will be the reduction in dentin hypersensitivity after the interventions. The findings of this study are expected to contribute to the identification of effective non-invasive treatment approaches for the management of dentin hypersensitivity associated with non-carious cervical lesions.
Key facts
- Study ID
- NCT07648147
- Run by
- Cukurova University
- People needed
- 30
- Starts
- 2026-07-20
- Expected to finish
- 2027-01-20
- Last updated by the study team
- 2026-06-15
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Individuals aged between 18 and 65 years. Systemically healthy individuals. Individuals with dentin hypersensitivity. Presence of two permanent teeth with similar severity of dentin hypersensitivity in the same participant.
- Participants who agree to participate in the study and sign the informed consent form
You may not qualify if…
- Presence of active caries in the study teeth. Presence of cervical restoration in the study teeth. Presence of pulpal pathology. History of desensitizing treatment within the last 3 months. Pregnancy. Presence of systemic disease. Use of analgesics within the last 48 hours.
Where it is running
- Çukurova University — Adana, sarıçam, Turkey (Türkiye)
Full record on ClinicalTrials.gov
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