GalaFlex Mesh in Facelift

Completed

Conditions studied: Superficial Musculoaponeurotic System (SMAS) Procedure

In brief

In this post market study a resorbable mesh (GalaFLEX) will be used to reinforce the lifted and imbricated SMAS along the suture lines and spread the load of the SMAS along a greater surface area. GalaFLEX mesh is comprised of resorbable 4-hydroxybutyrate fibers.

Key facts

Study ID

NCT02053831

Run by

C. R. Bard

People needed

15

Starts

2011-11-01

Expected to finish

2014-06-01

Last updated by the study team

2023-05-16

Who can join

Age: 21 and older, up to 99. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subject is able to understand the risks and benefits of participating in the study and must be willing to sign and date the Informed Consent Form for this study approved by the Institutional Review Board (IRB.)
• Be at least 21 years of age.
• Be willing and able to comply with the requirements of the protocol.
• Be willing to refrain from participating in any other investigational interventional study while enrolled in this study.
• Female subjects must have a negative pregnancy test within the last 24 hours timeline and have no intentions of becoming pregnant during participation in the study, or be sterilized.

You may not qualify if…

• Subject is unwilling or unable to give written consent to participate in the investigation or unable to comply with the requirements of the protocol.
• Subject has known severe allergies manifested by a history of anaphylaxis, or history or presence of severe multiple allergies.
• Subject has any serious skin disease, e.g., Eczema and psoriasis of the face, severe rosacea, scleroderma, local infections and severe acne.
• Subjects has diabetes, coagulation disorders, connective tissue disorders, lipodystrophy, or other serious systemic disease.
• Active herpes labialis
• Subject is infected with HIV and/or received or may receive immunosuppressive therapy over the course of the study (such as rheumatoid arthritis).
• Received any experimental drug or device within the previous three months.
• Known alcohol or drug abuser.
• Female subject who is pregnant or lactating or intending to become pregnant during the period of the study, or who would not use an adequate method of contraception (contraceptive pill, intra-uterine device) for the duration of the study.
• Possesses any psychological condition, or is under treatment for any condition which, in the opinion of the Investigator and/or consulting physicians(s),would constitute an unwarranted risk.
• Presents with severe jowling or severe cervical skin redundancy.
• Subject is currently a smoker or is a prior smoker who quit in the last 12 months.
• Active abscess or infection
• Currently involved with claims for, or is accepting, workers compensation
• Currently engaged in medical malpractice litigation.

Where it is running

• Ponte Vedra Plastic Surgery — Ponte Vedra Beach, Florida, United States
• The Few Institute for Aesthetic Plastic Surgery — Chicago, Illinois, United States
• Eye and Ear Institute — Chicago, Illinois, United States

Full record on ClinicalTrials.gov

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