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Efficacy of an Antiage Aesthetic Treatment for the Middle and Inferior Third of the Face

D

Derming

Status

Completed

Conditions

Face Skin Laxity

Treatments

Device: MonoDermà HA gel combined to a low level laser

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Primary endpoint of the study is to evaluate clinically and by non-invasive instrumental evaluations the aesthetic performance, on the third middle and inferior of the face, of "MonoDermà HA Bio-revitalizing gel", an intradermal filler containing hyaluronic acid, combined to a low level laser therapy (LLLT) to obtain a stable photo-cross-linking effect inside the dermis.

Enrollment

24 patients

Sex

Female

Ages

40 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • female sex;
  • Caucasian race;
  • non smokers;
  • no alcohol abuse and/or drug use;
  • 40-65 years;
  • FVLS 2-4 ;
  • available and able to return to the study site for the post-procedural follow-up examinations;
  • accepting not to change their habits regarding food, physical activity, cosmetic and cleansing products for the face;
  • accepting not to expose their face to strong UV irradiation (UV session and/or sun bathes) during the entire duration of the study, without appropriate sun protection;
  • accepting to sign the informed consent form.

Exclusion criteria

  • Pregnancy (only for female subjects not in menopause);
  • lactation (only for female subjects not in menopause);
  • smokers;
  • alcohol abuse and/or drug use;
  • female subjects not in menopause, who do not use adequate contraceptive precautions in order to avoid pregnancies during the study;
  • female subjects not in menopause, who do not accept to perform the pregnancy test at T0 and T1 (before the 1st and the 2nd aesthetic procedure);
  • Body Mass Index (BMI) variation (± 1) during the study period;
  • having performed face treatments for aesthetic correction (biomaterials implants, face lifting, botox injections, laser, chemical peeling) in the 6 months beginning of the study;
  • having used permanent filler in the past;
  • change in the normal habits regarding food, physical activity, face cosmetic, cleansing and make-up use during the month preceding the test;
  • sensitivity to the test filler or its ingredients, including delayed hypersensitivity to hyaluronic acid and granulomatous reactions (to be assessed by the investigator during the baseline);
  • subjects whose insufficient adhesion to the study protocol is foreseeable;
  • participation in a similar study currently or during the previous 9 months;
  • dermatitis;
  • presence of cutaneous disease on the tested area, as lesions, scars, malformations;
  • subjects that tend to develop hypertrophic scars;
  • 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 started more than 1 year ago);
  • using of drugs able to influence the test results in the investigator's opinion.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

24 participants in 1 patient group

MonoDermà HA gel combined to a low level laser
Experimental group
Description:
"Monodermà HA Bio-revitalizing gel" is a sterile, biodegradable, isotonic intradermal filler produced by Innate S.r.l. (Italy) and distributed by Giuliani S.p.A. (Italy) in non-pyrogenic pre-filled syringe of 2 ml containing 2% (20mg/ml) of medium chain (1.0-1.5 x 106 Dalton) hyaluronic acid (HA), obtained from bacterial fermentation, in a physiologic buffer (see Appendix 1) and used as a filler for the correction of deep skin sagging and roughness.
Treatment:
Device: MonoDermà HA gel combined to a low level laser

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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