The study to evaluate the efficacy and safety of linear high intensity focus ultrasound for lower face sagging in Thailand, A pilot study

Phase 4

Completed

• Conditions: Healthy human volunteers; High intensity focused ultrasound; Face; Skin

• Registration Number: TCTR20220629011
• Lead Sponsor: Dermatologic Surgery, Dermatology department, Siriraj hospital, Thailand

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2022-06-29
• Study Completion: 2023-04-03
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

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

Inclusion Criteria

1. Having skin laxity grading scale: grade 1-2.5
2. Thais

Exclusion Criteria

1. pregnant or lactating woman
2. Having the skin disease around the treated area
3. Using an energy-based device or other interventions around treated area 6 months prior

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Face volume loss Before the treatment, 2, 4, 8, 12, and 24 weeks after the treatment cc/Vectra 3d camera to evaluate the volume change

Secondary Outcome Measures

Name	Time	Method
Subject self assessment score Before the treatment, 2, 4, 8, 12, and 24 weeks after the treatment percentage of Subject self assessment score,Physicians assessment score Before the treatment, 2, 4, 8, 12, and 24 weeks after the treatment percentage of Physicians assessment score