Sponsored Interventional Single-center Study for the Assessment of the Efficacy and Tolerability of a Medical Device in Crema-gel for the Treatment of PEF (Edemato-fibrosclerotic Panniculopathy of 2nd and 3rd Degree)
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 56
- 试验地点
- 2
- 主要终点
- First day of study initiation: clinical history; personal and demographic data and previous or concomitant treatments
研究概览
简要总结
Post-marketing clinical study conducted on a CE medical device, named Defense Body, cellulite treatment, edematous fibrosclerotic panniculopathy (2nd and 3rd stage pathology), reducing draining cream-gel, to verify its effectiveness and tolerability on a panel of 56 subjects females affected by 2nd and 3rd degree PEF. The effectiveness of the device is measured in terms of reduction in thigh circumference, improvement in the appearance of the skin with reduction of the orange peel appearance and improvement in skin smoothness.
详细描述
Post-marketing, sponsored, interventional, single-centre clinical study conducted on a medical device, already CE marked, named Defense Body cellulite treatment edematous fibrosclerotic panniculopathy (2nd and 3rd stage pathology) draining reducing gel-cream, to verify the its efficacy and tolerability on a panel of 56 female subjects, aged between 18 and 55, in good general health, and suffering from 2nd and 3rd degree PEF.
A comparison study will be carried out between the clinical condition of the subjects at baseline T0, compared to the condition at the end of treatment T2, with provision for an intermediate visit halfway through treatment, T1.
At the first enrollment visit (T0), the patient will be subjected to anthropometric measurements, measurement of the skin profile of the thigh, measurement of the thigh circumference and evaluation by the clinician of the degree of cellulite using pinch tests and digital photographs of the area. treated in profile and three-quarter view.
After 4 (± 3 days) (T1) and 8 weeks (± 4 days) (T2) from the start of the study, the patient is visited again.
The Doctor will repeat the assessments described at T0, with the addition of verifying continued compliance with the enrollment criteria; overall evaluation by the patient of satisfaction and compliance; recording of each AE or AED or drop-off; recording of any concomitant pharmacological treatment.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 55 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Female sex;
- •Age between 18 and 55;
- •Presence of grade II or III symmetrical cellulite on the right and left lower limbs;
- •BMI between 18.5 and 30;
- •Good state of health and absence of chronic pathologies;
- •Willingness not to change one's lifestyle during study;
- •Willingness to join the study and sign the information consent.
排除标准
- •Subjects being treated with other topical products in the lower limbs;
- •Subjects being treated with other topical or systemic cellulite products;
- •Subjects with skin conditions and/or inflammatory conditions underway or had in the period immediately preceding the start of the study;
- •Subjects with a history of venous or lymphatic insufficiency in the lower limbs;
- •Subjects with known allergies or intolerances to one of the components of the product;
- •Pregnant or breastfeeding subjects;
- •Subjects undergoing slimming therapy, whether pharmacological or dietary;
- •Subjects who practice intense or competitive sporting activity.
结局指标
主要结局
First day of study initiation: clinical history; personal and demographic data and previous or concomitant treatments
时间窗: First day: within 24 hours
The following activities are planned on the first day: * clinical history of the recruited subjects; * personal and demographic data; * previous and/or concomitant treatments.
First day of study initiation: pinch test
时间窗: First day: within 24 hours
The clinician evaluates the degree of cellulite using a pinch test by applying pressure on the skin between thumb and index finger and assigns a grade from 0 to 4 according to a specific table.
First day of study initiation: digital photographs of the area to be treated
时间窗: First day: within 24 hours
digital photographs of the area to be treated, taken in profile and three-quarter view with a model camera Nikon Digital Camera.
First day of study initiation: Measurement of waist circumference, hip circumference and thigh circumference
时间窗: First day: within 24 hours
Measurement of: * waist circumference; * hip circumference * thigh circumference These measurements are taken using a flexible tape measure with the subject barefoot, in an upright position and, in the specific case of the measurement of the thigh, 1 cm below the crease of the buttock.
First day of study initiation: BMI
时间窗: First day: within 24 hours
Evaluation of height (cm) and weight (Kg) for the calculation of the body mass index, considered in the range 18.5 - 30.
First day of study initiation: skin profilemetry of the thigh
时间窗: First day: within 24 hours
Evaluation of the skin profilemetry of the thigh in a predetermined target area, through a computerized analysis Antera 3D CS Camera and 3.X software set (Mitavex, Dublin, Ireland). The images obtained allow the operator to measure the volume of protrusion and skin depressions in the area, expressed in mm3.
次要结局
- After 28 days of treatment: recording of any concomitant pharmacological treatments that have occurred.(On the 28th day of treatment)
- After 28 days of treatment: digital photographs of the area to be treated(On the 28th day of treatment)
- After 28 days of treatment: Measurement of waist circumference, hip circumference and thigh circumference(On the 28th day of treatment)
- After 56 days of treatment: recording of any concomitant pharmacological treatments that have occurred.(On the 56th day of treatment)
- After 56 days of treatment: digital photographs of the area to be treated(On the 56th day of treatment)
- After 56 days of treatment: skin profilemetry of the thigh(On the 56th day of treatment)
- After 56 days of treatment: pinch test(On the 56th day of treatment)
- After 56 days of treatment: overall rating of product satisfaction(On the 56th day of treatment)
- After 28 days of treatment: BMI(On the 28th day of treatment)
- After 56 days of treatment: AE or AED or Drop-off(On the 56th day of treatment)
- After 28 days of treatment: pinch test(On the 28th day of treatment)
- After 56 days of treatment: BMI(On the 56th day of treatment)
- After 28 days of treatment: skin profilemetry of the thigh(On the 28th day of treatment)
- After 28 days of treatment: AE or AED or Drop-off(On the 28th day of treatment)
- After 28 days of treatment: satisfaction evaluation and compliance(On the 28th day of treatment)
- After 56 days of treatment: Measurement of waist circumference, hip circumference and thigh circumference(On the 56th day of treatment)
- After 56 days of treatment: evaluation of compliance(On the 56th day of treatment)