Potassium Nitrate Gel and Diode Laser in the Treatment of Dentinal Hypersensitivity
NCT ID: NCT06923904
Last Updated: 2025-04-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
12 participants
INTERVENTIONAL
2025-04-15
2025-10-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Patients with dental sensitivity
With a split-mouth design the dental elements will be divided into the Trial group, treated with a 980 nm diode laser and desensitizing topical gel, and the Control group, treated only with the same gel.
Trial group, treated with a 980 nm diode laser and desensitizing topical gel
The study aims to evaluate the actual efficacy of diode lasers in laser desensitization by comparing the topical gel Emoform Actisens, containing 5% potassium nitrate, alone and in combination with a diode laser.
Interventions
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Trial group, treated with a 980 nm diode laser and desensitizing topical gel
The study aims to evaluate the actual efficacy of diode lasers in laser desensitization by comparing the topical gel Emoform Actisens, containing 5% potassium nitrate, alone and in combination with a diode laser.
Eligibility Criteria
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Inclusion Criteria
The exclusion criteria will be: (a) individuals taking pain relievers; (b) individuals undergoing orthodontic treatment; (c) non-vital teeth; (d) teeth with restorative materials; and (e) pregnant or breastfeeding women
18 Years
ALL
Yes
Sponsors
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University of Pavia
OTHER
Responsible Party
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Andrea Scribante
Associate Professor
Central Contacts
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Other Identifiers
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PotassiumNitrateLaser
Identifier Type: -
Identifier Source: org_study_id
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