Safety and Effectiveness of Style 410 Silicone-Filled Breast Implant Study | NCT00690339 | Trialant
CompletedInterventionalNot ApplicableUpdated Oct 13, 2014
Safety and Effectiveness of Style 410 Silicone-Filled Breast Implant Study
ClinicalTrials.gov ID
NCT00690339
Lead Sponsor
Allergan MedicalINDUSTRY
Overall Status
Completed
Study Type
Interventional
Phase
Not Applicable
Enrollment
941Actual
Last Update Posted
Oct 13, 2014Estimated
Start Date
Feb 2001
Primary Completion Date
Dec 2012Actual
Completion Date
Dec 2012Actual
Brief Summary
Safety and effectiveness of Style 410 Silicone-Filled Breast Implants in women undergoing primary augmentation, primary reconstruction, or revision of existing breast implants.
Breast Augmentation
Breast Reconstruction
Revision of Augmentation or Reconstruction
Style 410 Silicone-Filled Breast Implants
Ages Eligible for Study
Adult (18-64)Older Adult (65+)
Sexes Eligible for Study
Female
Accepts Healthy Volunteers
Yes
Eligibility Criteria
Inclusion Criteria:
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).
Exclusion Criteria:
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