- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05691049
Evaluation of Efficacy and Safety of HCC_45 for the Correction of Acne Scars of the Face
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
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.
Study Overview
Status
Intervention / Treatment
Detailed Description
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.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Adele Sparavigna, MD
- Phone Number: 0223183475
- Email: direzione.derming@gmail.com
Study Contact Backup
- Name: Roberto Lualdi, MD
- Phone Number: 0223183475
- Email: direzione.derming@gmail.com
Study Locations
-
-
Lombardia
-
Milano, Lombardia, Italy
- DERMING S.r.l., Clinical Research and Bioengineering Institute
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 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.
Exclusion Criteria:
- Dependent on the volunteers' characteristics:
- smokers;
- 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).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: HCC_45 treatment group
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. |
Dosage form: HCC_45 is a resorbable medical device 2 ml non-pyrogenic 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. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change from Baseline of Skin Roughness and flaccidity at 30 days and at 120 days post-injection
Time Frame: Day 0, Day 30, Day 120
|
Visual score from 1 (milder scarring) to 4 (severe scarring) (Goodman and Baron Grading Scale of Postacne Scarring)
|
Day 0, Day 30, Day 120
|
Change from Baseline of Skin's surface Profilometry at 30 days and at 120 days post-injection
Time Frame: 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.
|
Day 0, Day 30, Day 120
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Efficacy questionnaire
Time Frame: Day 120
|
Self assessment questionnaire regarding the efficacy of the study treatment on acne scars (score: very marked; marked; medium; light; absent;)
|
Day 120
|
Treatment tolerance questionnaire
Time Frame: Day 120
|
Self-assessment score: bad; poor; good; excellent
|
Day 120
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Adele Sparavigna, MD, DERMING S.r.l., Clinical Research and Bioengineering Institute
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- E0222
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Acne Scars - Mixed Atrophic and Hypertrophic
-
David SmartCompletedAcne Scars - Mixed Atrophic and HypertrophicUnited States
-
Syneron MedicalUnknownAcne Scars - Mixed Atrophic and HypertrophicUnited States
-
Alma LasersNot yet recruitingAcne Scars - Mixed Atrophic and HypertrophicPortugal
-
University of RochesterCompletedAcne Scars - Mixed Atrophic and HypertrophicUnited States
-
David SmartCompletedAcne Scars - Mixed Atrophic and Hypertrophic
-
Zagazig UniversityNot yet recruitingAcne Scars - Mixed Atrophic and Hypertrophic
-
Cutera Inc.CompletedAcne Scars - Mixed Atrophic and HypertrophicUnited States
-
Aarhus University HospitalBispebjerg HospitalUnknownAcne Scars - Mixed Atrophic and HypertrophicDenmark
-
Candela CorporationActive, not recruitingAcne Scars - Mixed Atrophic and Hypertrophic | WrinkleUnited States, Israel
-
Sofwave Medical LTDCompletedAcne Scars - Mixed Atrophic and HypertrophicUnited States