Effects of High Power Diode Laser Photobiomodulation on Bichat Ball Removal: a Split-Mouth Controlled Clinical Trial
- Conditions
- Adipose TissueE06.892
- Registration Number
- RBR-5g6jk5c
- Lead Sponsor
- niversidade Federal do Maranhão
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
aesthetic-functional need for bilateral partial surgical removal of the buccal fat pads; complaint of unilateral or bilateral nibbling on the buccal mucosa; complaint of disproportionality of the lower third of the face; good systemic health condition, therefore no comorbidities
present systemic comorbidities; smokers; pregnant or breastfeeding women; signs of any pre-operative inflammatory or infectious condition; are using any medication that interferes with the pain mechanism; history of allergies or adverse effects that prevent the use of medications that will be used in the study; present any significant facial asymmetry; have progressive hemifacial atrophy; underwent facial liposuction, lipolysis injection or bichectomy procedure prior to the research; they wish to have the surgery just for aesthetic reasons.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Effects of photobiomodulation of high-power diode laser in the postoperative period of removal of buccal fat pads (CAB).
- Secondary Outcome Measures
Name Time Method Analyze postoperative pain using a visual analogue scale (VAS); Analyze postoperative trismus by measuring maximum mouth opening with a Willis caliper; Evaluate the characteristics of the surgical wound through photographic images; From the photographic record of participants in pre-established conditions, analyze results on facial changes judged by evaluating photographs in pre- and post-operative moments (immediately, 7, 14, 30 and 6 months, 1 year); Evaluate the health-related quality of life of research participants on the 1st, 3rd, 5th and 7th postoperative days using the OHIP-14 questionnaire; Evaluate the aesthetic satisfaction of research participants in the pre- and post-operative period of 6 and 1 year using the FACE-Q scale.