Analysis of strategies for Dental Sensitivity reduction: a medical study

Phase 4

• Conditions: Dentin Sensitivity; C07.793

• Registration Number: RBR-10ksfmxx
• Lead Sponsor: Faculdade de Odontologia de Bauru - Universidade de São Paulo

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2024-01-12
• Last Update Posted: 23 January 2024
• Study Completion: 2025-02-01

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Participants who have at least one tooth with dentin hypersensitivity, with a score equal to or greater than 4 on the Analogic Visual Scale (VAS). Participants must be aged between 18 and 65. Both genders. Having overall good health. Being available to attend the scheduled appointments and treatment sessions throughout the study period

Exclusion Criteria

Individuals with active caries lesions and/or defective restorations on the selected and/or adjacent teeth; structural dentin loss requiring restoration or periodontal treatment; prior use of professional desensitizing agents in the last 6 months; smokers; pregnant individuals; those using anti-inflammatory and/or analgesic medications during the study period - or up to 72 hours before the initial assessment; those who regularly use anticonvulsants, antihistamines, sedatives, and/or anxiolytics; have orthodontic appliances; have a history of or current presence of neoplasms in the head and neck region; or are allergic to any component of the products used in the research

Study & Design

• Study Type: Intervention
• Study Design: Not specified