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临床试验/NCT03833687
NCT03833687已完成不适用

Aesthetic Performance and Tolerance Evaluation of an Injective Intradermal Treatment for the Skin Roughness and Laxity of Inner Arm and Abdomen

Derming SRL2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2018年9月11日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Derming SRL
入组人数
24
试验地点
2
主要终点
Change from baseline of photographic documentation

研究概览

简要总结

The objective of this study was to investigate the aesthetic performance of the Hyaluronic acid (HA)-based dermal filler Profhilo® injected by a novel bio aesthetic point technique ("BAP" technique) in woman aged 40-65 years with mild-moderate skin flaccidity and roughness of the abdomen and inner arms.

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
40 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • female sex;
  • age 40-65 years;
  • 3-4 abdomen and inner arm roughness/laxity grade according to a clinical reference scale;
  • asking for abdomen and inner arms laxity and roughness restoration;
  • available and able to return to the study site for the post-procedural follow-up examinations;
  • accepting to not change their habits regarding food, physical activity, cosmetic and cleansing products for the body;
  • accepting not to expose their face to strong UV irradiation (UV session, or sun bathes) during the entire duration of the study, without appropriate sun protection;
  • accepting to sign the informed consent form.

排除标准

  • Pregnancy;
  • lactation;
  • alcohol or drug abusers;
  • subjects not in menopause who do not use adequate contraceptive precautions in order to avoid pregnancies during the study;
  • subjects not in menopause who do not accept to perform the pregnancy test at T0 (before the 1st aesthetic procedure) and at T1 (1 month after the 1st injection treatment execution, before the 2nd aesthetic procedure);
  • Body Mass Index (BMI) variation (± 1) during the study period;
  • performing skin treatments for abdominal and brachial zone aesthetic correction (carboxytherapy injections, body lifting, laser, infrared light, bipolar radiofrequency, vacuum and mechanical massage) in the 6 months prior to the study start;
  • aesthetic surgical procedure on abdominal and brachial zone in the past;
  • change in the normal habits regarding food, physical activity, cosmetic products and cleansing for the body during the month preceding the test;
  • sensitivity to the test product or its ingredients (to be assessed by the investigator during the baseline visit);
  • subjects whose insufficient adhesion to the study protocol is foreseeable;
  • participation in a similar study currently or during the previous 6 months.
  • Dermatitis;
  • presence of cutaneous disease on the tested area, as lesions, scars, malformations;
  • recurrent facial/labial herpes;
  • clinical and significant skin condition on the test area (e.g. active eczema, psoriasis, severe rosacea, scleroderma, local infections and severe acne).
  • Diabetes;
  • endocrine disease;
  • hepatic disorder;
  • renal disorder;
  • cardiac disorder;
  • pulmonary disease;
  • neurological or psychological disease;
  • inflammatory/immunosuppressive disease;
  • drug allergy.
  • Anticoagulants and antiplatelet drugs, anti-histaminic, topic and systemic corticosteroids, narcotic, antidepressant, immunosuppressive drugs (with the except of contraceptive or hormonal treatment starting more than 1 year ago);
  • using of drugs able to influence the test results in the investigator opinion.

结局指标

主要结局

Change from baseline of photographic documentation

时间窗: Baseline (T0), 1 month (T1), 4 months (T2)

2D pictures of the abdomen and inner arm

Change from baseline of arm skin roughness and laxity clinical grade

时间窗: Baseline (T0), 1 month (T1), 4 months (T2)

Skin roughness and laxity clinical grade, according to a visual score from 1 (no roughness and flaccidity) to 5 (very severe roughness and flaccidity).

Change from baseline of abdomen skin roughness and laxity clinical grade

时间窗: Baseline (T0), 1 month (T1), 4 months (T2)

Skin roughness and laxity clinical grade, according to a visual score from 1 (no roughness and flaccidity) to 5 (very severe roughness and flaccidity).

Change from baseline of deep skin hydration

时间窗: Baseline (T0), 1 month (T1), 4 months (T2)

Tissue dielectric constant value of superficial and deep skin layers was measured mono-laterally on the right or left inner arm and hemiabdomen with MoistureMeterD (Delfin Technologies, Kuopio - Finland)

Change from baseline of skin density

时间窗: Baseline (T0), 1 month (T1), 4 months (T2)

A little skin area of about 7 cm2 (at level of inner arm was pinched, in standardized conditions, using a specific device. Because of this "pinch" the skin profile changes depending on cutaneous density; when the skin is slack the "pinch" forms a lot of wrinkles. A picture of the skin pinched was taken thanks to Primos compact portable device (GFMesstechnik); Primos software is able to measure skin principal profilometric parameters.

Change from baseline of skin plastoelasticity

时间窗: Baseline (T0), 1 month (T1), 4 months (T2)

Superficial and deep skin plastoelasticity was measured mono-laterally on the right or left inner arm and hemiabdomen with the instrument Dermal Torque Meter (Dia-Stron Ltd., UK).

Change from baseline of superficial skin hydration

时间窗: Baseline (T0), 1 month (T1), 4 months (T2)

Skin electrical capacitance value was measured mono-laterally on the right or left inner arm and hemiabdomen with Corneometer CM825 (Courage - Khazaka, Köln, Germany). The measure of the skin capacitance properties is an indirect expression of its hydration level.

次要结局

未报告次要终点

研究者

发起方
Derming SRL
申办方类型
Other
责任方
Principal Investigator
主要研究者

Adele Sparavigna

Medical Doctor

Derming SRL

研究点 (2)

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