Thigh Circumference Reduction Study
Stopped early · Not applicable
Conditions studied: Reduction of Localized Excess Fat
In brief
The purpose of this study is to evaluate the Cutera radio frequency (RF) device for the new indication of reduction of thigh circumference.
Key facts
- Study ID
- NCT00953290
- Run by
- Cutera Inc.
- People needed
- 4
- Starts
- 2009-01-01
- Expected to finish
- 2010-01-01
- Last updated by the study team
- 2011-05-10
Who can join
Age: 18 and older, up to 70. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Body Mass Index between 20 and 35
- Presence of cellulite grades II, III or IV according to GLD scale
- Visible bi-lateral thigh fat Thigh area to be treated to measure at least 30.0mm in vertical fold, as measured with industry standard fat caliper
- Subject must be able to read, understand and sign the Consent Form
- Subject must adhere to the follow-up schedule and study instructions
- Subject must adhere to the same diet and/or exercise routine throughout the study
You may not qualify if…
- Significant weight fluctuation (+/-10 lbs) in the past 6 months
- Taking weight-loss medications/supplements
- Participation in any other clinical study
- Cellulite treatment within 3 months of the treatment
- Surgical or non-surgical treatments to the target area in the last 12 months, e.g., liposuction
- Prior treatment to the target area within the last 12 months
- Arteriosclerosis or weakened blood vessels
- Heart disease
- Thromboembolic disease
- Diagnosed or documented immune system disorders
- Bleeding disorders.
- Presence of uncontrolled hypertension
- Taking prescription anticoagulants
- History of keloid formation
- Malignant tumors in the target area
- Diabetes
- Any disease or condition that could impair wound healing
- Skin abnormalities in the target area, e.g., cuts, scrapes, wounds, scars
- Infection in the target area
- Implanted electrical device(s)
- Pregnant or lactating
Where it is running
- Blackhawk Plastic Surgery — Danville, California, United States
Full record on ClinicalTrials.gov
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