Influence of low-level laser therapy on cheek fat removal on face measures, satisfaction with facial aesthetics and quality of life: a clinical trial

Not Applicable

Recruiting

• Conditions: Cheek; A01.456.505

• Registration Number: RBR-8cyqk93
• Lead Sponsor: Centro Universitário Christus - UNICHRISTUS

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-05-10
• Study Completion: 2023-02-03
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

Healthy individuals (American Society of Anesthesiologists - ASA I) of both sexes; aged between 18-30 years; with the need to partially remove the buccal extension of the Bichat ball bilaterally

Exclusion Criteria

Smoking volunteers; pregnant or lactating women; signs of any preoperative inflammatory or infectious condition; systemic diseases

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary outcome of the present study will be the perception of postoperative pain using a 10-point visual analogue scale in the first seven days after the surgical procedure. Pain assessment will be performed considering the right and left sides. The differences obtained between the preoperative values and those obtained in the postoperative evaluations (24 hours, 7 days, 1 month, 3 months and 6 months) will be compared.