Pulse oximeter evaluation in the reading of tooth oxygenatio

Not Applicable

• Conditions: Pathological conditions, signs and symptoms; Pulpitis; Dental Pulp Necrosis; C07.793.237.820; C07.793.237.315

• Registration Number: RBR-68xbth
• Lead Sponsor: niversidade Federal de Santa Catarina

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-09-04
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Data analysis completed
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Healthy volunteers; non smokers; both genders; intact permanent teeth without cavities or restorations; teeth with pulp vitality without internal resorption or calcification; teeth with complete root apex without signs of periodontal or periapical lesions

Exclusion Criteria

Smoking patients; patients who suffered external tooth whitening; patients with parafunctional habits; patients with a history of dental trauma; pregnant women; lactating women; patients using orthodontic appliances; patients with previous dental pain

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
It is expected to find changes in the pulp oxygen saturation levels, observed with the use of the pulse oximeter, from the observation of a variation of at least 5% in the pre and post-intervention measurements (use of the bleaching gels).

Secondary Outcome Measures

Name	Time	Method
It is expected to verify less dental sensitivity with the use of the whitening gel associated with the desensitizer, by comparing the results obtained between the whitening gels, after the filling of the analogue pain scale by the patients, from the finding of a variation of at least 5% in the patients. pre- and post-intervention results.<br>;Check the increase in the painful sensitivity of the dental elements, with the use of an analogue pain scale completed by the patient after each intervention, based on the observation of a variation of at least 5% in the pre and post-intervention measurements.