Multiple CoolSculpting Treatment Study

Completed · Not applicable

Conditions studied: Body Fat Disorder

In brief

To evaluate the safety of same-day CoolSculpting treatments and to assess the impact on serum lipids and liver-related tests.

Key facts

Study ID

NCT01814007

Run by

Zeltiq Aesthetics

People needed

35

Starts

2013-03-01

Expected to finish

2013-10-22

Last updated by the study team

2021-05-17

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Male or female subjects > 18 years of age.
• Subject who has been assessed to receive multiple CoolSculpting treatments on the abdomen and flanks, defined as follows:
• Lower Abdomen - One 60 minute cycle with CoolMax,
• Right and Left Flank - One 60 minute cycle per flank, with CoolCurve+ or CoolCore, simultaneously.
• Subject has not had weight change exceeding 10 pounds in the preceding month.
• Subject with body mass index (BMI) up to 30. BMI is defined as weight in pounds multiplied by 703 divided by the square of the height in inches.
• Subject agrees to not making any major changes in their diet or lifestyle during the course of the study.
• Subject has read and signed a written informed consent form.

You may not qualify if…

• Subject has had an invasive (e.g., liposuction, mesotherapy, abdominoplasty) or non-invasive fat reduction and/or body contouring procedure in the area of intended treatment within the past 6 months.
• Subject needs to administer, or has a known history of subcutaneous injections into the area of intended treatment (e.g., heparin, insulin) within the past month.
• Subject has a known history of cryoglobulinemia, cold urticaria, or paroxysmal cold hemoglobinuria.
• Subject has a history of hernia in the area(s) to be treated.
• Subject is pregnant or intending to become pregnant during the study period (in the next 4 months).
• Subject is lactating or has been lactating during the past 3 months.
• Subject is unable or unwilling to comply with the study requirements, such as blood draw.
• Subject is currently enrolled in a clinical study of any other unapproved investigational drug or device.
• Subject has a history of lipodosis or other confounding metabolic diseases.
• Subject is taking or has taken medication within the past 3 months which may affect the metabolic function.
• Patient has a history of diabetes.
• Any other condition or laboratory value that would, in the professional opinion of the investigator, potentially affect the subject's response or the integrity of the data or would pose an unacceptable risk to the subject.

Where it is running

• Innovation Research Center — Pleasanton, California, United States
• Ed Becker, MD — Walnut Creek, California, United States
• Bowes Dermatology Group — Miami, Florida, United States

Full record on ClinicalTrials.gov

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