Fat Reduction in the Flanks Area vs. Control

Exclusion Criteria

• •1. History of hypertension, ischemic heart disease, valvular heart disease, congestive heart failure, pacemaker/defibrillator, abdominal aortic aneurism
• •2. Known hyperlipidemia, diabetes mellitus, hepatitis, liver disease, HIV positive status, blood coagulopathy or excessive bleeding, autoimmune or connective tissue disease
• •3. Having or undergoing any form of treatment for active cancer, or having a history of skin cancer or any other cancer in the areas to be treated, including presence of malignant or pre-malignant pigmented lesions
• •4. Having any active electrical implant anywhere in the body, such as a pacemaker or an internal defibrillator
• •5. Having a permanent implant in the treated area, such as metal plates or an injected chemical substance such as silicone
• •6. Having undergone any other surgery in the treated areas within 12 months of treatment or during the study, including liposuction
• •7. Previous body contouring procedures in the treatment area within 12 months
• •8. History of skin disease in the treatment area, known tendency to form keloids or poor wound healing
• •9. Suffering from significant skin conditions in the treated areas or inflammatory skin conditions, including, but not limited to, open lacerations or abrasions and active cold sores or herpes sores prior to treatment (duration of resolution as per the Investigator's discretion) or during the treatment course
• •10. Skin lesions in the treatment area other than simple nevi on physical examination (e.g., atypical nevus, tattoo, abrasions) including depressed scars in the treatment area
• •11. Very poor skin quality (i.e., severe laxity)
• •12. Abdominal wall diastasis or hernia on physical examination
• •13. Abnormal kidney, liver or coagulation functions, abnormal lipid profile or blood count within the last 3 months
• •14. Obesity (BMI above 30)
• •15. Childbirth within the last 12 months or breastfeeding women. Any acute or chronic condition which, in the opinion of the investigator, could interfere with the conduct of the study
• •16. Unstable weight within the last 6 months (i.e., ± 3% weight change in the prior six months)
• •17. Fat thickness lower than 2.5 cm after strapping at the treated area.
• •18. Participation in another clinical study involving same anatomical areas within the last 6 months (or 30 days in case different anatomical areas were treated in previous trial/s).
• •19. As per the Investigator's discretion, any physical or mental condition which might make it unsafe for the subject to participate in this study.