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The use of a Topical Anesthetic (EMLA) to assess decreased pain during the Periodontal Probing exam

Phase 1
Conditions
C07.465.714
Chronic Periodontitis
Registration Number
RBR-8h7b5dw
Lead Sponsor
niversidade Estadual de Ponta Grossa
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruitment completed
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Volunteers aged between 18 and 60 years; of both genders, with at least five teeth in each hemi-arch (including 16, 22, 36 and 32); who had probing sensitivity and features of chronic periodontitis with probing depth greater than or equal to 5mm

Exclusion Criteria

Use of prophylactic antibiotics before periodontal probing; psychiatric disorders or chronic pain; clotting disorders; anticoagulation therapy; pregnant or lactating women; congenital or idiopathic methemoglobinemia; treatment with methemoglobin inducing agents; allergic to anesthetics; use of steroidal or non-steroidal anti-inflammatory drugs in the three days prior to the start of the study and patients with acute periodontal pain, pulpitis, abscesses or other acute infections

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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