Clinical Performance of B-Lite® Light Weight Breast Implant

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.

Study Overview

• Status: Active, not recruiting
• Conditions: Breast Implants
• Intervention / Treatment: Device: B-Lite- Light Weight Breast Implants

• Study Type: Interventional
• Enrollment (Estimated): 120
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Germany
  • Heidelberg, Germany
    • ETHIANUM
• Israel
  • Herzliya, Israel
    • Herzelia Medical Center
• Sweden
  • Stockholm, Sweden
    • Akademikliniken

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 14 years to 56 years (Adult)
• Accepts Healthy Volunteers: Yes

Description

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

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: procedure with B-Lite® Light Weight Breast Implant	Device: B-Lite- Light Weight Breast Implants

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Changes in breast size measurements	3 years
Changes in bra size measurements	3 years

Collaborators and Investigators

• Sponsor: G&G Biotechnology Ltd.

Study record dates

Study Major Dates

• Study Start (Actual): October 1, 2016
• Primary Completion (Estimated): December 1, 2026
• Study Completion (Estimated): December 1, 2028

Study Registration Dates

• First Submitted: April 21, 2016
• First Submitted That Met QC Criteria: May 17, 2016
• First Posted (Estimated): May 19, 2016

Study Record Updates

• Last Update Posted (Estimated): September 4, 2025
• Last Update Submitted That Met QC Criteria: August 28, 2025
• Last Verified: August 1, 2025

More Information

Terms related to this study

• Other Study ID Numbers: CL-010

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• product manufactured in and exported from the U.S.: No