跳至主要内容
临床试验/NCT05691049
NCT05691049已完成不适用

Interventional, Post-marketing, Local, Mono-centric Study for Evaluation of Efficacy and Safety of HCC_45 for the Correction of Acne Scars of the Face

IBSA Farmaceutici Italia Srl1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2022年11月24日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
1
主要终点
Change from Baseline of Skin Roughness and flaccidity at 30 days and at 120 days post-injection

研究概览

简要总结

Acne scars represent a frequent complication of moderate/severe acne and may negatively impact on psychosocial and physical well-being of acne patients. Several types of acne scars have been classified and the same patient is likely to have more than one type. Each type can be treated with varying degrees of success. The main acne scars are the following:

Atrophic or Depressed Scarring:

  • Ice pick: An ice pick scar has a wide shaft that narrows down to the tip. It resembles a hole that's wide at the top and narrows to a point as it goes deeper into the skin. Such an indentation is common and one of the most challenging scars to heal. This scar is more frequent on forehead and upper cheeks, where skin is thinner.
  • Rolling: These scars are typically found on the lower cheeks and jaw, where skin is thicker. The indents have sloping edges that makes the skin look uneven and wavy.
  • Boxcar: Boxcar scars are indents that have sharper edges. Those edges go down deep into the skin. These scars are common on the lower checks and jaw.

详细描述

Open label clinical trial, conducted by 1 center under dermatological control.

Primary aim of the study is to evaluate the efficacy and the safety of the deep injection of HCC_45 in acne scars of the face (ice picks, rolling, boxcars).

Secondary endpoint is self-assessment questionnaire regarding treatment efficacy and tolerance.

HCC_45 is a resorbable medical device 2 ml nonpyrogenic pre-filled syringe, containing 2 ml of hyaluronic acid for intradermal use. The principal component of the medical device is Hyaluronic Acid of non-animal origin, produced by bacterial fermentation.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •caucasian subjects of both sexes;
  • •age >18years
  • •asking for acne scars treatment;
  • •presenting acne scars (ice picks, rollings, boxcars);
  • •available and able to return to the study site for the post-procedural follow-up examinations;
  • •agreeing to present at each study visit without make-up;
  • •accepting to not change their habits regarding food, physical activity, make-up use, face cosmetic and cleansing products;
  • •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

  • •Dependent on the volunteers' characteristics:
  • •performing in the 6 month before the trial beginning HA injections, radiofrequency treatment, toxin treatment;
  • •contraindication or know allergy to the devices' components or to the treatment;
  • •participation in a similar study actually or during the previous 3 months
  • •known pregnancy
  • •occurrence of pregnancy during the study
  • •Dependent on a clinical condition: Dermatological disease:
  • •Dermatitis;
  • •presence of cutaneous disease on the tested area,different from those under study
  • •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).
  • •Dependent on a clinical condition: General disease:
  • •Diabetes, coagulation disorders, connective tissue disorders, lipodystrophy or other systemic disease;
  • •HIV and/or immunosuppressive disease;
  • •cancerous or precancerous lesions in the either right or left midface;
  • •severe allergies manifested by a history of anaphylaxis, or history or presence of severe multiple allergies;
  • •alcohol or drug abusers;
  • •Dependent on a pharmacological treatment:
  • •Anti-inflammatory drugs, anti-histaminic, topic and systemic corticosteroids, narcotic, antidepressant, immunosuppressive drugs (with except of contraceptive or hormonal treatment starting more than 1 year ago);
  • •assumption of drugs able to influence the test results in the investigator opinion.
  • •The use of other drugs, not mentioned above, can be authorized by the Investigator. The trade name, the dosage, the start and stop date of the therapy will be reported on Case Record Form (CRF).

研究组 & 干预措施

HCC_45 treatment group

Experimental

Treatment of acne scars of the face by using a subcision+injection technique: the needle (25 G) or cannula (25 G) (wider areas are treated with the cannula) is inserted into the skin and made to move with a back-and-forth motion in order to detach scar collagen bundles. Then 1 syringe (2 ml) of HCC_45 is injected.

Day 0: Information and consent form provided, Clinical assessment, Digital clinical pictures, Instrumental assessment, Profilometry measurement.

First treatment of HCC_45 (refer to study protocol).

Day 30 (1 month after day 0): Clinical assessment, Digital clinical pictures, Instrumental assessment, Profilometry measurement.

Second treatment of HCC_45 (refer to study protocol).

Day 120 (4 months after day 0): Clinical assessment, Digital clinical pictures, Instrumental assessment, Profilometry measurement.

NO treatment, Self-evaluation questionnaire.

干预措施: HCC_45 (Device)

结局指标

主要结局

Change from Baseline of Skin Roughness and flaccidity at 30 days and at 120 days post-injection

时间窗: Day 0, Day 30, Day 120

Visual score from 1 (milder scarring) to 4 (severe scarring) (Goodman and Baron Grading Scale of Postacne Scarring)

Change from Baseline of Skin's surface Profilometry at 30 days and at 120 days post-injection

时间窗: Day 0, Day 30, Day 120

A measurement of the skin surface affected by acne scars is taken thanks to Primos compact portable device (GFMesstechnik); Primos software is able to measure skin principal profilometric parameters in vivo or on skin replicas, the software compares directly the different images obtained at the times foresee by the protocol.

次要结局

  • Treatment tolerance questionnaire(Day 120)
  • Efficacy questionnaire(Day 120)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

Evaluation of Efficacy and Safety of HCC_45 for the... | 临床试验