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Evaluation of the Dental Root Sensitivity treatment comparing two types of products

Evaluation of the Efficacy of Dentinic Hypersensitivity treatment using two types of Desensitizing Agents

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-67645p
Enrollment
Unknown
Registered
2019-03-20
Start date
2018-02-04
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

Treatment of dentin hypersensitivity in areas of root exposure (gingival recession) with the application of two desensitizing products that will be compared: Test: glass ceramic (Biosilicate) and cont

Sponsors

Univerdade Federal de Goiás
Lead Sponsor
Faculdade de Odontologia da Universidade Federal de Goiás
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Participants should present at least 2 teeth with dentin hypersensitivity and that have not had root scraping in the last 6 months; nor treatment for dentin hypersensitivity in the last 6 months

Exclusion criteria

Exclusion criteria: those participants with a very acidic diet; pregnant or lactating; patients who use chronic analgesics or anti-inflammatories; dentures fixed or removable dentures; patients with orthodontic appliances

Design outcomes

Primary

MeasureTime frame
Expected outcome 1: Reduction of dentin sensitivity for both groups, by the mean difference of the initial and final VAS value (Visual Analog Scale). Reduction of at least 5 points in the value of the EVA scale for each group;Expected outcome 2: It is expected that there will be greater reduction on dentin sensitivity for the biosilicate group, in comparison to Duraphat group

Secondary

MeasureTime frame
Secondary outcomes are not expected

Countries

Brazil

Contacts

Public ContactVirgilio Roriz

Faculdade de Odontologia da Universidade Federal de Goiás

vmroriz@hotmail.com+55 (62) 3209-6051

Outcome results

None listed

Source: REBEC (via WHO ICTRP)