NCT00399854已完成4 期
Clinical Study for Evaluation of the Efficacy of Mechanical Massage by Endermologie (Dhermia® - Industra Mecânica Fina Ltda) in Treatment of Cellulite and Body Contouring
Hexsel Dermatology Clinic0 个研究点目标入组 45 人开始时间: 2006年3月1日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 45
- 主要终点
- Assessment of effectiveness of treatment based on current classification of cellulite and evaluation of the corporal measures
研究概览
简要总结
The purpose of this study is to perform a clinical assessment of the efficacy of the device DHERMIA® (Industra Mecânica Fina Ltda)in the treatment of cellulite and body contouring
详细描述
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 25 Years 至 45 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •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.
排除标准
- •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.
结局指标
主要结局
Assessment of effectiveness of treatment based on current classification of cellulite and evaluation of the corporal measures
次要结局
- Assessment of subject's satisfaction
- Visual assessments of the treated area before and after treatment
- Safety analysis
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