Safety and Efficacy Evaluation of Sodium Hyaluronate 32mg/ml in Improving Facial Skin Dryness and Dullness

IBSA

Status

Enrolling

Conditions

Facial Dryness

Facial Dullness

Treatments

Device: Sodium Hyaluronate

Study type

Interventional

Funder types

Industry

Identifiers

NCT06914583

23CHN-Pro-IT01

Details and patient eligibility

About

The aim of the study is to evaluate the safety and efficacy of sodium hyaluronate 32 mg/ml in improving facial skin dryness and dullness. Subjects are randomized to the treatment group or to the control group. Only subjects in the treatment group are treated by intradermal injection.

Full description

This is a prospective multi-center clinical investigation. Enrolled subjects are randomized to the treatment group or to the no-treatment control group. The treatment group will receive intradermal injections of sodium hyaluronate 32 mg/ml. The improvement of facial skin dryness and dullness will be evaluated at multiple timepoints.

Enrollment

500 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Age ≥18 years old and ≤65 years old (based on the time of signing the ICF), gender is not restricted;
Skin Fitzpatrick is classified as type II-IV;
Subjects who are seeking temporary improvement of their dry facial skin and dull complexion. The investigator has assessed the subjects are suitable for receiving injectable treatment to improve these conditions;
Subjects who have agreed not to use any other medical cosmetic treatments related to the study during the study period;
Subjects who voluntarily sign a written informed consent form, and able to comprehend the full nature and the purpose of the investigation, including possible risks and side effects, and subjects able to cooperate with the investigator and to comply with the requirements of the entire investigation (including ability to attend all the planned investigation visits according to the time limits), based on investigator's judgement.

Exclusion criteria

Known allergy to hyaluronic acid or any component of this product;
Known history of severe allergies;
Known history of severe autoimmune disease;
Subjects with episode of herpes cutis;
Subjects with cicatricial diathesis;
Facial area has unknown injection substances;
Have received any permanent or semi-permanent fillers at the facial area (e.g., calcium hydroxyapatite, poly-L-lactic acid, polymethyl methacrylate, silicones, expanded polytetrafluoroethylene (ePTFE), polycaprolactone, etc.), autologous fat, face lift (including thread lifts), etc., or plan to receive any of the above treatments during the investigation;
Have received temporary dermal filler treatment (e.g., cross-linked hyaluronic acid, collagen) at the facial area within the 12 months prior to enrolment, or plan to receive any of the above treatments during the investigation;
Have received botulinum toxin injection, mesotherapy, or facial cosmetic procedures (e.g., facial liposuction, cosmetic surgery, face slimming, photo modulation therapy, intense pulsed light, radiofrequency, non-cross-linked hyaluronic acid injection (except for mesotherapy), dermabrasion, laser or chemical peels or other ablation procedures, etc.) at facial area within 6 months prior to enrolment, or plan to receive any of the above treatments during the investigation;
Have received sodium hyaluronate compound solution injection (mesotherapy, etc) at facial area within 3 months prior to enrolment,
Facial area has active or progressive skin infection (including viral, bacterial, fungal);
Facial area has skin granuloma;
Facial area has active or progressive skin diseases or with isomorphic reactions such as acute eczema, flat warts, lichen planus, psoriasis vulgaris, etc.;
Facial area has malignant tumors or skin tumors of unknown nature;
Subjects who work outdoors for a long time or need to be exposed to sunlight after surgery;
Patients with excessive expectations for treatment effects;
Subjects with coagulation dysfunction or other systemic diseases;
Subjects undergoing chemotherapy/radiotherapy;
Subjects with mental illness or emotional instability;
Subjects who had received any thrombolytic agents, anticoagulants or antiplatelet drugs within 2 weeks before enrolment;
Subjects who are pregnant or planned to become pregnant during the investigation period, or breastfeeding;
Subject who participated in other clinical investigation within 1 month prior to enrolment in this investigation, or currently participating in other clinical investigation;
The investigator considers that the subject is not suitable to participate in this clinical investigation.