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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03833687
Other study ID # E0918
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 11, 2018
Est. completion date February 6, 2019

Study information

Verified date February 2019
Source Derming SRL
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date February 6, 2019
Est. primary completion date February 6, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 40 Years to 65 Years
Eligibility Inclusion Criteria:

- 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.

Exclusion Criteria:

- Pregnancy;

- lactation;

- smokers;

- 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;

- cancer;

- 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.

Study Design


Related Conditions & MeSH terms

  • Skin Flaccidity and Roughness of the Abdomen and Inner Arms

Intervention

Device:
Profhilo®
Profhilo® (IBSA Farmaceutici Italia S.r.l.) is a resorbable medical device 2.25 ml non-pyrogenic pre-filled syringe, containing 2 ml of 3.2% hyaluronic acid for intradermal use (32 mg H-HA + 32 mg L-HA dissolved in 2 ml of saline buffered sodium chloride.

Locations

Country Name City State
Italy DERMING Milano MI

Sponsors (1)

Lead Sponsor Collaborator
Derming SRL

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline of arm skin roughness and laxity clinical grade Skin roughness and laxity clinical grade, according to a visual score from 1 (no roughness and flaccidity) to 5 (very severe roughness and flaccidity). Baseline (T0), 1 month (T1), 4 months (T2)
Primary Change from baseline of abdomen skin roughness and laxity clinical grade Skin roughness and laxity clinical grade, according to a visual score from 1 (no roughness and flaccidity) to 5 (very severe roughness and flaccidity). Baseline (T0), 1 month (T1), 4 months (T2)
Primary Change from baseline of superficial skin hydration 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. Baseline (T0), 1 month (T1), 4 months (T2)
Primary Change from baseline of deep skin hydration 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) Baseline (T0), 1 month (T1), 4 months (T2)
Primary Change from baseline of skin density 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. Baseline (T0), 1 month (T1), 4 months (T2)
Primary Change from baseline of skin plastoelasticity 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). Baseline (T0), 1 month (T1), 4 months (T2)
Primary Change from baseline of photographic documentation 2D pictures of the abdomen and inner arm Baseline (T0), 1 month (T1), 4 months (T2)