Post-Menopause Skin Rejuvenation Study

This study is a prospective, controlled, open-label study involving fifty (50) post-menopausal adult female participants between the age of 40 and 65, who are both utilizing and not utilizing Hormone Replacement Therapy (HRT) to control post-menopausal symptoms. All participants with facial or décolleté skin aging will be considered eligible for treatment following completion of the informed consent process and Baseline evaluation.

Randomization (as primary participant complaint) will be undertaken to allocate participants to one of two groups:

• Group A (Hydration as Primary Complaint): HASBV followed by PLLA-SCA (n = 25)
• Group B (Laxity as Primary Complaint): PLLA-SCA followed by HASBV (n = 25)

Inclusion criteria

• Participants must voluntarily sign and date an informed consent, approved by an independent ethics committee, prior to the initiation of any screening or study-specific procedures.
• post-menopausal participants between the age of 40 and 65 years old;
• Participants with a -menopausal status (at least 12 consecutive months of amenorrhea without other pathological or physiological causes).

• A clinical evaluation will be undertaken by a clinical professional to determine post-menopausal status.
• Participants with established clinical signs of skin aging including but not limited to: reduced skin elasticity, increased wrinkling, dryness, volume loss and/or contour deficits.
• Participant is willing and able to comply with procedures required in the protocol.
• Participant must be in good health as per investigator's judgment based on medical history
• For subgroup analysis: either currently on stable-dose HRT for ≥ 6 months or not receiving any form of HRT for ≥6 months

Exclusion criteria

• Previous biostimulators 18 months prior to this study;
• Previous SP-HA 18 months prior to this study;
• Previous HA injectables 18 months prior to study in the facial and décolleté region;
• Participant has an uncontrolled systemic disease.
• Participant presents with or has a history of any medical condition that may place the participant at an increased risk following exposure to hyaluronic acid or interfere with the study evaluation, including:

• Diagnosed myasthenia gravis, Lambert-Eaton syndrome, amyotrophic lateral sclerosis, or any other significant disease that might interfere with neuromuscular function
• History of facial nerve palsy
• Infection or dermatological condition at the treatment injection sites
• Marked dermatochalasis, deep dermal scarring, excessively thick sebaceous skin, or excessively photodamaged skin
• Participant has a history of clinically significant medical conditions or any other reason that the investigator determines would interfere with the participant's participation in this study or would make the participant an unsuitable candidate to receive the study medical device.
• Participant has a history of an allergic reaction or significant sensitivity to constituents of the study medical device (or its excipients) including Vicryl
• Participant has an tattoos, jewellery, or clothing which obscure the treatment area and cannot be removed.
• Participant has an anticipated need for surgery or overnight hospitalization during the study.
• Participant has a history of surgical procedures in intended treatment areas, including any lifting procedure (e.g., facial lift, suture lift, thread lift, brow lift, eyelid and/or eyebrow surgery, neck lift).
• Participant with known active COVID infection within 14 days of baseline treatment.
• Participant is currently enrolled in another clinical study.
• Participant is presenting with porphyria.
• Participant presents with active disease, such as inflammation, infection or tumors, in or near the intended treatment sites.
• Participant has a bleeding disorder or take thrombolytics or anticoagulants.
• Participant has a need to take immunosuppressants.
• Participant has undergone dental procedures including teeth cleaning withing 14 days prior to baseline treatment
• Participant has undergone any vaccine administration withing the 14 days prior to treatment administration
• Participant categorised as a heavy smoker, more than 12 cigarettes per day