Efficacy and safety of monopolar Radiofrequency for treatment of lower facial laxity in Asia

Phase 4

Recruiting

• Conditions: Healthy; Monopolar radiofrequency; Laxity

• Registration Number: TCTR20210326002
• Lead Sponsor: Faculty of Medicine Siriraj Hospital, Mahidol University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-03-26
• Study Completion: 2021-09-24
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Healthy volunteer with lower face laxity
BMI < 25 kg/m2
mild to moderate lower face laxity

Exclusion Criteria

- Pregnancy or breastfeeding
- Had any electronically, magnetically, or mechanically activated implant
- Swollen, infected, or inflamed facial skin
- History of herpes infection
- Current smoking
- Previous facial treatment of botulinum toxin or radiofrequency or focused ultrasound within 6 months
- Previous facial treatment of filler within 12 months

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Face volume baseline, immediate, 1 month, 3 month, 6 month after treatment VECTRA3D analysis,Physician improvement scale immediate, 1 month, 3 month, 6 month after treatment quartile grading scale,Patient satisfaction scale immediate, 1 month, 3 month, 6 month after treatment quartile grading scale

Secondary Outcome Measures

Name	Time	Method
Safety immediate, 1 month, 3 month, 6 month after treatment Adverse event