NCT07007351: HEBE8

Multicenter, Prospective Study to Determine the Performance and Safety of the New M-HA30 Architect Device on the Quality of the Skin: HEBE8 Study

Completed NA Last updated 5 June 2025

What this trial tests

NA trial testing Intradermal injection in Skin Aging in 285 participants. Completed in 13 June 2024.

Timeline

19 March 2023

Primary endpoint
13 April 2024

13 June 2024

Quick facts

Lead sponsor	Laboratoires FILLMED
Phase	NA
Status	Completed
Study type	INTERVENTIONAL
Allocation	randomized
Design	parallel
Masking	single
Primary purpose	other
Enrollment	285
Start date	19 March 2023
Primary completion	13 April 2024
Estimated completion	13 June 2024
Sites	1 location across France

Drugs / interventions tested

• Intradermal injection

Conditions studied

• Skin Aging — all drugs for Skin Aging →

Sponsor

Laboratoires FILLMED

Who can join

Adults 19 to 84, any sex, with Skin Aging. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

For skin rejuvenation the targeted population does not present a specific pathology. Aesthetic procedures are requested by the patient to improve appearance, look younger and feel better.

Non-crosslinked Hyaluronic acid (HA) is widely used by intradermal multiple injection as it is a glycosaminoglycan, which binds and retains water thus improving the wrinkles while the tone and elasticity of the skin.

Previous studies showed that an important administration of Si had benefic effects on bone development, skin ageing and fragile hair and nails.

The major issue of the Si intake is the rapid absorption and excretion, and consequently low effects on the skin. Moreover, with ageing, gastric pH become more acidic and decreases the conversion capacity of the Si.

All these data together led Laboratoires Fillmed to develop an HA product boosted by Si to inject into ther dermis in order to fill fine lines wrinkes and improve skin quality.

This study aims to demonstrate the efficacy of this new Hyaluronic Acid based filler versus a reference device, with an intradermal multi-injection technique, on reducing the superficial wrinkles measured by comparative evaluation between baseline and D30+10 of the evolution of wrinkles of the face / neck and décolleté by clinical scoring.

To this end, subjects in whom a correction of wrinkles of the face and/or décolleté and/or neck is sought, will be included. Subjects will receive 2 sessions of treatment on each side of the concerned area and the aesthetic correction will be appreciated at 10 ± 2 days (D30+10) following the last treatment session and the maintenance of the correction will be evaluated on D60, D120 and D180.

Main objective:

The main objective of this randomized study is to demonstrate objectively the effectiveness of the studied device, on the reduction of the universal wrinkles score, performed in presence of the subjects, between baseline and D30+10 (10 days after the last injection) on the cheeks, neck or décolleté and its non-inferiority by intraindividual comparison versus a reference device for the cheek and the neck.

Secondary objectives:

* For all groups and for the concerned zones:

\- to assess the efficacy of the devices between baseline and D180 (including D0, D30+10, D60, D120 and D180) and comparatively evaluate the efficacy for the cheeks and neck of the tested device compared to the reference device on:
* the Universal Wrinkles Score performed on the cheek's wrinkles, neck wrinkles or décolleté's wrinkles by the investigators, in presence of the subjects
* Zone-specific (cheek, neck or décolleté) clinical scores performed from photographical visual scales, Clinical score of radiance (for the face)
* the Universal Wrinkles Score performed at the end of the study in a blind manner by an expert on the cheek's wrinkles, neck wrinkles or décolleté's wrinkles from the standardized photographs

\- to assess the efficacy of the devices from D30 to D180 on the Global Aesthetic Improvement Scores performed by:
* the investigator (IGAIS) for 5 items
* the subjects (SGAIS) for 5 items

* to assess the safety, efficacy and the opinion of the subjects by a questionnaire
* to illustrate the efficacy of the devices by standardized photographs

Three Research Centerswere added to the study to have objective and instrumental data on the efficacy of the products on skin's:

* hydration by Corneometer®
* firmness and elasticity by CutoMeter®
* density by Ultrasound Imaging
* anatomical characteristics by in vivo Reflectance Confocal Microscopy
* anatomical characteristics by in vivo Optical Coherence Tomography
* the average volume of wrinkles (depth and surface) measured on the cheeks from image processing performed from 3D imaging

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.