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
- HealthyElectrical multidirectional stimulationEMDSAbdominal contouring
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
Name Time Method Abdominal mass 1 mo MRI
- Secondary Outcome Measures
Name Time Method Abdominal contouring 1 mo, 2 mo, 3 mo photograph