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The effect of laser application and desensitizing gel in the treatment of dentinal hypersensitivity

Protocols for the treatment of Dentinal Hypersensitivity with Low-level Laser and Potassium Nitrate in a risk group: a longitudinal clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-977fm24
Enrollment
Unknown
Registered
2022-03-03
Start date
2019-09-01
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

Dentin Sensitivity

Interventions

At the first visit, study participants will receive verbal instructions about the study, including all procedures involved. Each study participant will also be informed of the possible risks involved
E07.632.490

Sponsors

Faculdade de Odontologia da Universidade de São Paulo
Lead Sponsor
Faculdade de Odontologia da Universidade de São Paulo
Collaborator

Eligibility

Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Both genders, aged between 18 and 45 years old; have good general health; agree to participate in accordance with the Informed Consent Form (TCLE); present at least one tooth with Hypersensitivity reported in the cervical region, which will have to have a graded sensitivity equal to or greater than 4 on the VAS scale

Exclusion criteria

Exclusion criteria: Present active carious lesions or with defective restorations in the tooth to be analyzed; have enough dentin loss that requires restorative treatment; having undergone any professional desensitizing treatment in the past 6 months; use of desensitizing pastes within 3 months; use of anti-inflammatory drugs or analgesics at the time of recruitment; volunteers who are pregnant or breastfeeding

Design outcomes

Primary

MeasureTime frame
Cervical dentin hypersensitivity level after evaporative stimulation; Analysis Method: Visual Analog Scale.

Secondary

MeasureTime frame
Secondary outcomes are not expected

Countries

Brazil

Contacts

Public ContactAna Cecilia Aranha

Faculdade de Odontologia da Universidade de São Paulo

acca@usp.br+55 (11) 3091 7843

Outcome results

None listed

Source: REBEC (via WHO ICTRP)