Evaluation of the Efficacy of Endermologie in Treatment of Cellulite and Body Contouring

The present study is a clinical, opened trial and single-center.

The patients were treated by endermologie device. Mechanical massage were performed for 12 weeks in a total of 24 treatment sessions: twice a week.

A set of photographs were took at visit 1 (baseline), visit 2, 3 and 4 with standardized positions and lighting conditions.

Inclusion criteria

• Written Informed Consent;
• Subjects agreeing to take part of all procedures of the study (including mechanical massage, photographs), after being fully informed on the objectives and nature of the investigations;
• Female subjects between 25-45 years;
• Subjects presenting with cellulite grades I-III on buttocks and thighs;
• Medical history and physical examination which, based on the investigator's opinion, do not prevent the patient from taking part in the study and use the device under investigation;
• Female subjects of childbearing age should present a negative urine pregnancy test and should be using an effective contraceptive method (3 months before the enrollement untill the end of the study);
• Body Mass Index (BMI = weight/height2) beetwen 20,0-25,0 and 25,0-29,9;
• Availability of the subject throughout the duration of the study (90 days);
• Availability of the subject in maintaining a stable weight during the study (variation less than 2 kg)
• Subjects with sufficient schooling and awareness to enable them to cooperate to the degree required by this protocol.

Exclusion criteria

• Pregnant women or women intending to become pregnant during the study (next 3 months);
• BMI superior 30,0;
• Subjects with diabetes mellitus, cardiac insufficiency, asthma, or bronchitis;
• Subjects participating in other clinical trials;
• Subjects with neoplastic disorders, uncontrolled thyroid disorders or uncontrolled hypertension;
• Subjects with coagulation disorders, using anticoagulants or tendency of bruises;
• Subjects with vascular disorders (phlebitis or varicose veins) in the area to be treated;
• Any prior aesthetic surgery affecting the area to be treated (liposuction, Subcision®), 3 months before the study, that may interfere with results;
• Any other prior anti-cellulite treatment or body measures treatment, 30 days prior to the study;
• Subjects with inflammation or active infection in the area to be treated.
• Subjects with a history of adverse effects, which in the investigator's opinion should prevent the patient from participating in the study;
• Patients with cutaneous or vascular alterations, that difficult visualization and documentation of cellulite;
• Subjects with a history of medical treatment non-adherence or showing unwillingness to adhere to the study protocol;
• Subjects who can not come to the visits (one missing visit/ month is allowed);
• Subjects intending to initiate any intensive sport;
• Subjects using analgesics, non-hormonal antiinflammatories, antihistaminics, corticosteroids, or diuretics;
• Subjects tanned, or intending to expose the area of study to sun, artificial UV, or self-tanning during the study;
• Any condition that, in the opinion of the investigator, can compromise the evaluation of the study.