CompletedNot Applicable

A Comparison of Long-Term Effectiveness of Two Desensitizing Products

Turkey (Türkiye)50 participantsStarted 2019-02-01

Plain-language summary

This randomized, controlled, clinical trial aimed to compare the 6- month clinical performance of a desensitizer that contains calcium phosphate TM with a two-step self-etch adhesive SE and placebo (distilled water). At least 150 teeth wil be treated with desensitizing products and placebo randomly one third usig TM, one third using SE and one third using placebo. The efficiency of the materials will be evaluated at baseline, 1 week, 1 month, 3 months and 6 months after treatment.

Who can participate

Age range18 Years – 70 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓. Subjects with 3 or more hypersensitive teeth with a VAS (Visual Analog Scale) score
✓. Willingness to participate in the study

Exclusion criteria

✕. Subjects are unwilling to participate voluntarily
✕. Patients under 18 years old
✕. Those that were taking analgesic medicaments
✕. Pregnant and breastfeeding females
✕. The presence of a systemic disease that affects the participation
✕. Teeth with cervical loss of hard tissue that need restoration absolutely
✕. Large/defective restoration, caries or enamel cracks in sensitive teeth
✕. Teeth with vulnerability to hypersensitivity after root scaling

What they're measuring

The effectiveness of desensitizers through long-term period

Timeframe: 6 months

Trial details

NCT IDNCT03851900

SponsorBaskent University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-10-01

View on ClinicalTrials.gov More Dentin Hypersensitivity trials