The primary objective of this protocol is the continued collection of data specific to the submental, inner thigh and back/bra body areas with CoolSculpting Elite. The study aims to collect post-market safety data while allowing for the collection of standardized photos and satisfaction questionnaires after treatment with commercial treatment parameters.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
102
CoolSculpting Elite Applicator
Pacific Clinical Innovations
Vista, California, United States
Number of Participants with Device and/or Procedure-Related Adverse Events (AEs)
Frequency of device and procedure-related AEs including serious device-related adverse events (SADEs), will be analyzed per cohort.
Time frame: Up to Approximately 6 Months
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