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The efficacy and safety of electrical multi-directional stimulation (EMDS) alone and the combination of EMDS and non-invasive radiofrequency for abdominal contouring

Phase 4
Recruiting
Conditions
Healthy
Electrical multidirectional stimulation
EMDS
Abdominal contouring
Registration Number
TCTR20200605003
Lead Sponsor
Faculty of Medicine Siriraj Hospital, Mahidol University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
26
Inclusion Criteria

Healthy volunteer age 18-60 years

Exclusion Criteria

Patients were not treated if they had contraindications to the truSculpt flex, including cardiac pacemaker, known myocardial arrhythmia, swollen, infected, or inflamed skin, or cancer. Additionally, patients were excluded if they had any electronically, magnetically, or mechanically activated implant; if they had any metal implant; skin abnormality; cancer treatment within the prior three months; history of seizure disorder or epilepsy, or pregnancy.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Abdominal mass 1 mo MRI
Secondary Outcome Measures
NameTimeMethod
Abdominal contouring 1 mo, 2 mo, 3 mo photograph
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