Formaderm (Hyaluronic Acid) for Facial Soft Tissue Augmentation

NCT ID: NCT05822778

Last Updated: 2023-04-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 98 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-02-13
• Study Completion Date: 2015-06-30

Brief Summary

The goal of this clinical trial is to evaluate the safety and efficacy of Formaderm (hyaluronic acid) dermal filler injection for soft tissue augmentation. The main questions it aims to answer are:

• The differences of Wrinkle Severity Rating Scale (WSRS) after the injection.
• The differences of Global Aesthetic Improvement Scale (GAIS) after the injection.
• The subjective satisfaction of treatment.
• Safety Indicators of which incidences on the day of the injection or after the injection.

Participants will be self-controlled and randomized for same period

• received both trial product and control product at the same time.
• re-visited on week 2, 4, 12, 24, 36, and 52 after injection.

Researchers will compare if the test product is non-inferiority to Q-Med Restylane.

Detailed Description

The purpose of this study is to evaluate the safety and efficacy of Formaderm (hyaluronic acid) dermal filler injection for soft tissue augmentation. A single-centre, non-inferior, randomized, double-blind trial with a control group was conducted in this study. Every subject received the trial product and control product injections at the same time. It was planned to recruit 95 subjects with the 10% dropout rate. This clinical trial is accordance with the "Good Clinical Practice (GCP) issued by the Department of Health and ISO14155-1：2003 Clinical investigation of medical devices for human subjects - Part 1: General Requirements and carried out according to the trial proposal approved by the Tri-Service General Hospital Human Subjects Review Committee.

Conditions

Dermal Filler

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: DOUBLE

Study Groups

Formaderm(FD) group

Formaderm was randomly administered either side of subjects' facial areas once. The injection volume was limited to 2c.c.

Group Type: EXPERIMENTAL

Formaderm Dermal Filler Injection

Intervention Type: DEVICE

Dermal filler injection to facial areas

control group

As a self-controlled study, "Q-MED" RESTYLANE would be administered on the other side after injected Formaderm. The injection volume was limited to 2c.c.

Group Type: ACTIVE_COMPARATOR

"Q-MED" RESTYLANE

Intervention Type: DEVICE

Dermal filler injection to facial areas

Interventions

Formaderm Dermal Filler Injection

Dermal filler injection to facial areas

Intervention Type: DEVICE

"Q-MED" RESTYLANE

Dermal filler injection to facial areas

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Subjects are aged 30-65 years old of both sexes.
• Subjects who are willing to undergo WSRS therapy.
• The WSRS baseline measurement should be 3-4 points and the left and right side should be in symmetry.
• The facial skin is healthy, without any disease that possibly interferes with skin aging status assessment.
• The subject is willing to avoid undergoing other cosmetic treatment and surgery, including Botox injection.

Exclusion Criteria

• Women subjects who are pregnant, breastfeeding, planning to become pregnant, and not willing to take contraception during the trial period.
• Those who are emotionally unstable or suffering from a mental disease.
• Those who have severe skin disease, inflammation, or related symptoms such as infections, psoriasis, herpes, and the like.
• Those who have undergone cosmetic treatment or surgery prior to the trial:
• Those who have undergone laser treatment or dermabrasion within the past 12 months.
• Those who have undergone chemical peels treatment within the last three months.
• Those who have undergone facial wrinkle augmentation surgery such as Botox injections within the past 12 months.
• Those with silicone in their body or material that cannot be absorbed by the body (permanent filling agent).
• Those who have undergone facial surgery or filing agent implants in the nasolabial fold area within the past 24 months.
• Those who have a scar or localized infection in the nasolabial fold area.
• Those with connective tissue diseases.
• Those with diabetes or systemic disease that cannot be controlled.
• Those suffering from human immunodeficiency syndrome.
• Those suffering from immunity related disorder or have had immune system degradation in the past.
• Those with a scar-prone constitution, prone to scar formation or hypertrophic scars.
• Those who have joined other clinical trials such ass medical device related and other similar trials within the past six months.
• Those with a medical history of cosmetic filling agent allergy, any type of hyaluronic acid implants, or drugs (such as antibiotics, antihistamine, non-steroidal anti-inflammatory analgesics), or those with a medical history of local anesthetic allergy.
• Patients undergoing anticoagulant treatment, those who have a medical history of coagulation defects, or those taking Chinese medicine for promoting blood circulation.
• Those whose medication and medical conditions are deemed unfit for inclusion in the research based on the judgment of the researcher.
• Those who are unable to comply with re-visit schedule or are unwell to sign the informed consent.

• Minimum Eligible Age: 30 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Maxigen Biotech Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

2-102-05-113

Identifier Type: -

Identifier Source: org_study_id