The primary objective of this study is to demonstrate the efficacy and safety of the carbon dioxide for subcutaneous fat reduction.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
25
Northwestern University
Chicago, Illinois, United States
Reduction of flank circumference
Time frame: 6 months
10-point pain visual analog scale
Time frame: 4 weeks
Any adverse events
Time frame: 6 months
Patient satisfaction, determined by using patient satisfaction questionnaires.
Time frame: 6 months
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