Expired Study
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Chicago, Illinois 60611


Purpose:

This study intends to investigate and compare the changes that may occur in response to cryolipolysis (localized cool exposure) and subcision (surgical technique) on cellulite. The cryolipolysis cooling device that will be used is FDA approved for skin cooling, but still investigational in the treatment of cellulite. It has previously been used for fat reduction on love handles or back fat. During cryolipolysis, the system will draw fat tissue into an applicator then expose the extracted fat tissue to cold temperatures. The cold exposure causes fat cells to die, with the goal to decrease the raised areas of cellulite. Subcision is a process used to treat scars left behind by acne or other skin diseases and has been noted to improve moderate to severe cellulite. Subcision is a simple surgical procedure that is performed by inserting a specially designed needle under the skin after local numbing medication is injected. The needle is moved in a repetitive motion parallel to the skin to separate the surface tissue from the deeper scar tissue with the goal to improve the dimpling caused by these tissues sticking together. This study is a pilot study designed to determine feasibility of these procedures.


Criteria:

Inclusion Criteria: - Healthy female patients 18-60 years of age with more than one evident depressed lesion of cellulite on the upper thighs and/or buttocks. - All subjects must have the affected areas that show the mattress phenomenon spontaneously when standing or while both lying and standing (Stage 2 or 3 of Nurnberger-Muller grading scale of cellulite7). - Subjects who are willing and have the ability to understand and provide informed consent for participation in the study and are able to communicate with the investigator. Exclusion Criteria: - Pregnant or lactating - Subjects who are unable to understand the protocol or to give informed consent. - Subjects currently under treatment with an antiplatelet or anticoagulant for any medical problem or patients who have coagulation disorder. - Subjects who have a known history of cold-induced disease such as cryoglobulinemia, paroxysmal cold hemoglobinuria, or cold urticaria. - Subjects who have active skin disease or skin infection in treatment area. - Subjects who are allergic to lidocaine or prilocaine. - Subjects who are allergic to both cephalexin (and penicillin) AND levofloxacin (or another quinolone antibiotic). - Subjects who have history of abnormal scarring.


NCT ID:

NCT01209767


Primary Contact:

Principal Investigator
Murad Alam, MD
Northwestern University


Backup Contact:

N/A


Location Contact:

Chicago, Illinois 60611
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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