For Healthcare Professionals

Safety Follow-up Study in Subjects With Silicone Gel-filled Breast Implants as Compared Both to Saline-filled Breast Implants and to National Norms

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About the study

Ten year safety study examining rates of rare adverse events, child bearing issues, effects of mammography, MRI compliance and results, and long-term benefit of silicone-filled breast implants.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

  1. revision) with Allergan silicone implants or saline breast implants (
  2. controls) OR - age 22 or older who is a candidate for breast augmentation (primary or
  3. revision) with Allergan silicone implants or saline breast implants (
  4. controls) - Exhibit fluency and literacy in English or Spanish Enrollment Criteria - Have satisfied all the inclusion and none of the

EXCLUSION CRITERIA

  1. Are transgender
  2. If a saline implant subject, have a current or past unilateral or bilateral silicone gelfilled breast implant
  3. Investigator decision that subject is not a suitable candidate for a long-term observational study
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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall 844-663-3742Email iconEmail Study Center

Study’s details


Contition

Breast Implant

Age

18+

Participants needed

56460

Est. Completion Date

Dec 2029

Treatment type

Observational


Sponsor

Allergan

ClinicalTrials.gov identifier

NCT00443274

Study number

BIFS-001

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