Clinical Performance of B-Lite® Light Weight Breast Implant

G&G Biotechnology

Status

Enrolling

Conditions

Breast Implants

Treatments

Device: B-Lite- Light Weight Breast Implants

Study type

Interventional

Funder types

Industry

Identifiers

NCT02777476

CL-010

Details and patient eligibility

About

This is a post-marketing study for B-Lite® implants that carry the EC certificate for marketing in Europe and AMAR certificate for marketing in Israel. To date, thousands of implants have already been implanted in women. The study is open for primary augmentation patients only. All surgeries will be performed as per standard practice at the given study site. No parallel surgical procedures will be performed at the same session.

Enrollment

120 estimated patients

Sex

Female

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Genetic women between the ages of 18 and 60 seeking primary breast augmentation
Patient is eligible to undergo MRI (i.e., no implanted metal or metal devices, no history of severe claustrophobia)
Patient provides signed informed consent
Patient agrees to comply with the study protocol and complete all required follow up visits, including to undergo MRI
Patient agrees to return the device to the Sponsor should the implant have to be explanted
The patient has realistic expectations of surgical results after discussion with investigator and is an acceptable candidate for breast augmentation.

Exclusion criteria

Patients with active infection anywhere in their body
Patient is pregnant or nursing at the time of recruitment, or has been in the 6 months preceding recruitment date, or not willing to use reliable means of contraception during the first year after surgery
Patient was implanted with any silicone implant other than breast implants (e.g., silicone artificial joints or facial implants)
Patient breast tissue is clinically incompatible for the procedure (e.g., tissue damage resulting from radiation, insufficient tissue coverage or compromised vascularity)
Patient has a condition, or is under treatment for any condition, which, in the opinion of the investigator and/or consulting physician(s), may constitute an unwarranted surgical risk (e.g., unstable cardiac or pulmonary problems, possible allergies and/or extraordinary immune response to implant)
The patient has a history of mental instability and/or history of pharmaceutical psychiatric treatment
Patient unable to understand the scope of the study and/or surgery
The patient has any disease, including uncontrolled diabetes (e.g., HbA1c > 8%), that is clinically known to impact wound healing ability
Patient has existing costal injuries
Patient has abscesses, malignant tumors (cancer or recurrent metastases), clinically relevant cysts or advanced fibrotic disease or patient with BIRAD ≥3
Are not willing to undergo further surgery for revision, if medically required
The patient has a confirmed rheumatic disease or syndrome (e.g., SLE, Sjogren's syndrome, scleroderma, polymyositis or any connective tissue disorder, rheumatoid arthritis, crystalline arthritis, infectious arthritis, spondyloarthropathies, any other inflammatory arthritis, fibromyalgia or chronic fatigue syndrome)
The patient has a severe breast and upper trunk deformity
The patient participated in an investigational trial within 90 days of enrollment
The patient has undergone an invasive medical procedure within 90 days of enrollment.
Aesthetic addiction, drug abuse, alcohol abuse