Safety and Effectiveness of Style 410 Silicone-Filled Breast Implant Study

Completed · Not applicable

Conditions studied: Breast Augmentation, Breast Reconstruction, Revision of Augmentation or Reconstruction

In brief

Safety and effectiveness of Style 410 Silicone-Filled Breast Implants in women undergoing primary augmentation, primary reconstruction, or revision of existing breast implants.

Key facts

Study ID

NCT00690339

Run by

Allergan Medical

People needed

941

Starts

2001-02-01

Expected to finish

2012-12-01

Last updated by the study team

2014-10-13

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Female, age 18 years or older
• Patients seeking primary breast augmentation (i.e., no previous breast implant surgery) indicated for the following: Patient dissatisfaction with size or shape of breast (e.g., mammary hypoplasia), asymmetry, ptosis, aplasia
• Patients seeking breast reconstruction
• Patients seeking breast revision-augmentation
• Patients seeking breast revision-reconstruction
• Adequate tissue available to cover implants
• Patients must be willing to undergo MRI at their 1, 3, 5, 7, and 10-year follow-up visits (serial MRI). The patient must be eligible for MRI (for example, no implanted metal or metal devices and no history of severe claustrophobia that may make her ineligible for MRI).

You may not qualify if…

• Advanced fibrocystic disease considered to be premalignant without accompanying subcutaneous mastectomy
• Existing carcinoma of the breast, without mastectomy
• Abscess or infection in the body at the time of enrollment
• Pregnant or nursing
• Have any disease, including uncontrolled diabetes (e.g., Hb AIc > 8%), that is clinically known to impact wound healing ability
• Show tissue characteristics that are clinically incompatible with mammaplasty, such as tissue damage resulting from radiation, inadequate tissue, compromised vascularity or ulceration
• Have, or under treatment for, any condition that may constitute an unwarranted surgical risk (e.g., unstable cardiac or pulmonary problems)
• Show psychological characteristics that may be incompatible with the surgical procedure and the prosthesis, such as inappropriate attitude or motivation (e.g., body dysmorphic disorder)
• Are not willing to undergo further surgery for revision, if medically required

Where it is running

• Study site — Indianapolis, Indiana, United States

Full record on ClinicalTrials.gov

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