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

This study has been completed.
Information provided by (Responsible Party):
Allergan ( Allergan Medical ) Identifier:
First received: June 2, 2008
Last updated: October 6, 2014
Last verified: December 2013
Safety and effectiveness of Style 410 Silicone-Filled Breast Implants in women undergoing primary augmentation, primary reconstruction, or revision of existing breast implants.

Condition Intervention
Breast Augmentation Breast Reconstruction Revision of Augmentation or Reconstruction Device: Style 410 Silicone-Filled Breast Implants

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)

Resource links provided by NLM:

Further study details as provided by Allergan ( Allergan Medical ):

Primary Outcome Measures:
  • Local Complications [ Time Frame: 10 years ]
    By patient risk of complications occurring in at least 5% of patients in 1 or more cohorts

Secondary Outcome Measures:
  • Satisfaction With Breast Implants as Determined by Patients and Physicians on a 5-point Scale. [ Time Frame: 10 years ]
    Satisfaction score on a 5-point scale, where 1 is definitely dissatisfied and 5 is definitely satisfied

Enrollment: 941
Study Start Date: February 2001
Study Completion Date: December 2012
Primary Completion Date: December 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: 1
Device: Style 410 Silicone-Filled Breast Implants
Breast Implant Surgery
Experimental: 2
Device: Style 410 Silicone-Filled Breast Implants
Breast Implant Surgery
Experimental: 3
Device: Style 410 Silicone-Filled Breast Implants
Breast Implant Surgery
Experimental: 4
Device: Style 410 Silicone-Filled Breast Implants
Breast Implant Surgery


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT00690339

United States, Indiana
Indianapolis, Indiana, United States
Sponsors and Collaborators
Allergan Medical
  More Information

Responsible Party: Allergan Medical Identifier: NCT00690339     History of Changes
Obsolete Identifiers: NCT00557674
Other Study ID Numbers: 00201
Study First Received: June 2, 2008
Results First Received: December 17, 2013
Last Updated: October 6, 2014 processed this record on September 21, 2017