Influence of different products on the effectiveness and duration of treatment of sensitive teeth and patients' well-being

Not Applicable

Recruiting

• Conditions: Dentin sensitivity; C07.465

• Registration Number: RBR-109h3wcv
• Lead Sponsor: niversidade Federal de Uberlândia

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-05-02
• Last Update Posted: 27 May 2024
• Study Completion: 2026-03-20

Recruitment & Eligibility

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

Inclusion Criteria

Patients with dentin hypersensitivity in at least 3 teeth with loss of tooth structure of less than 1mm; moderate to severe dentin hypersensitivity (pain greater than 3); Individuals who are interested in the treatment of dentin hypersensitivity; agree to participate and sign the free and informed consent form; participants aged between 18 and 60

Exclusion Criteria

Presence of dentin sensitivity caused by the presence of caries or unsatisfactory restorations; patient undergoing orthodontic or periodontal treatment; patients undergoing teeth whitening; presence of spontaneous pain in the tooth with dentin hypersensitivity, characterizing pulpitis; presence of periodontal disease; poor and unsatisfactory oral hygiene; use of extensive prostheses; patients with severe bruxism and changes in vertical dimension; patients with uncontrolled gastroesophageal reflux disease; patients with uncontrolled systemic or psychological illnesses; patients who use controlled medications that interfere with salivary flow; pregnant and lactating women; smokers

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
It is expected that the universal adhesive system and flow resin as obliterating agents improve the effectiveness and durability of the treatment of dentin hypersensitivity when compared to the use of potassium nitrate associated with glutaraldehyde, control group

Secondary Outcome Measures

Name	Time	Method
Evaluate the periodontal condition of patients, determined through clinical assessment before the intervention and within 7, 30, 90 and 180 days for follow-up;Evaluate patients' quality of life, determined through the quality of life questionnaire, before the intervention and within 90 and 180 days for follow-up