Evaluation of different potassium oxalate concentrations in teeth hypersensitivity

Not Applicable

Recruiting

• Conditions: Stomatognathic diseases, tooth abrasion, dentin sensitivity, tooth erosion; C07.793.818.124; C07.793.266; C07.793.818.500

• Registration Number: RBR-3pr9pp
• Lead Sponsor: Hospital Odontológico da Universidade Federal de Uberlândia

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-08-07
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

The criteria for inclusion of the patients will be: healthy individuals who are interested in the treatment of Dentin Hypersensitivity; Agree to participate and sign the informed consent form (TCLE); Patients with all teeth in their mouth; Patients with at least two teeth with Dentin Hypersensitivity in different quadrants.

Exclusion Criteria

The criteria for exclusion of patients will be: presence of dentin hypersensitivity caused due to the presence of caries or unsatisfactory restorations; Patients in orthodontic or periodontal treatment; Patients performing dental whitening; Presence of spontaneous pain in the tooth with dentin hypersensitivity, characterizing pulpitis; Presence of periodontal disease; Unsatisfactory oral hygiene; Use of extensive prostheses; Patients with severe bruxism and loss of vertical dimension; Patients with uncontrolled gastroesophageal reflux disease; Patients with uncontrolled systemic and / or psychological diseases; Pregnancy and smokers.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduction in dentin hypersensitivity in patients<br>submitted to different concentration with twotypes of potassiun oxalate in 3 weeks follow-up. The evaluation will be carried out by visual analogy scale of pain from the observation of a range of at least 30% in the pre and post intervention measurements.

Secondary Outcome Measures

Name	Time	Method
To determine an effective treatment protocol for reduction in dentin hypersensitivity, regarding the desensitizing agent concentration.The effectiveness evaluation will be carried out by visual analogy scale.