Comparison of the efficacy and safety of surgical laser with electrocautery in the treatment of gingiva increase by denture

Not Applicable

Recruiting

• Conditions: Gingival hyperplasia; Gingival and edentulous alveolar ridge lesions associated with trauma.; C07.465.714.258.428.250; K06.2

• Registration Number: RBR-27fpmt
• Lead Sponsor: niversidade federal de Minas Gerais

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-03-02
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Healthy volunteers; age greater than 18 years; both genders; with clinical diagnosis inflammatory fibrous hyperplasia.

Exclusion Criteria

Volunteers using analgesic medication; with systemic diseases.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Comparison of the efficacy and safety of surgical diode laser with electrocautery in the treatment of inflammatory fibrous hyperplasia, evaluated by the following parameters:<br>postoperative bleeding (according to the indexes: absent, discrete, moderate and intense, the amount of anesthesia used, edema and postoperative pain (visual analogue scale), tissue healing (measurement of the healed area and / or scarring). According to scientific literature, both treatments presents 100% of lesion resolution, and will be observated for 4 weeks postoperative. Lesions with several sizes present the same treatment efficacy and safety. From the statistical analysis, it will be possible to verify if there are differences in postoperative surgical characteristics, as well as the most effective and safe technique for the treatment of inflammatory fibrous hyperplasia.

Secondary Outcome Measures

Name	Time	Method
Secondary outcomes are not expected.