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Pulse oximeter evaluation in the reading of tooth oxygenation

Pulse oximeter evaluation in oxygen saturation reading of the dental pulp

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-68xbth
Enrollment
Unknown
Registered
2020-09-04
Start date
2017-08-18
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pathological conditions, signs and symptoms

Interventions

Experimental group: 17 patients underwent tooth whitening of the anterior, upper and lower teeth (112 teeth in total). Each patient had the pulp vitality of the teeth measured by the pulse oximeter, b
Other
E06.420.750

Sponsors

Universidade Federal de Santa Catarina
Lead Sponsor
Programa de Pós-Graduação em Odontologia
Collaborator

Eligibility

Age
18 Years to 25 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.;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.

Countries

Brazil

Contacts

Public ContactDilma Henriques

Universidade Federal de Santa Catarina

henridilma8@hotmail.com+55-048-37215840

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 13, 2026