A Pilot Study Testing a Noninvasive Cryolipolysis Device Versus a High Intensity Focused Ultrasound Device for Fat Reduction

Exclusion Criteria

• •1. Pregnant or lactating or intends to become pregnant in the next 9 months.
• •2. Unable to understand the protocol or to give informed consent.
• •3. Any previous and/or pending procedures at the treatment area or that may likely affect the treatment area.
• •4. Pending and/or anticipated major change in diet or exercise pattern in the six weeks following the last treatment or who has taken diet pills within the last 6 months..
• •5. History of asthma or chronic obstructive pulmonary diseases.
• •6. Active skin disease or skin infection in the treatment area.
• •7. Bleeding tendency or coagulopathy.
• •8. Subjects who are allergic to lidocaine.
• •9. Any other condition that would, in the professional opinion of the investigator, potentially affect response or participation in the clinical study, or would pose as an unacceptable risk to the subject.