Indianapolis, Indiana, United States
NCT Number: NCT00690339
Safety and Effectiveness of Style 410 Silicone-Filled Breast Implant Study
Safety and effectiveness of Style 410 Silicone-Filled Breast Implants in women undergoing primary augmentation, primary reconstruction, or revision of existing breast implants.
Looking for future studies?
Notify MeKey information
Age range
18 year and older
Sex eligibility
Female
Study type
Interventional
Phase
Not applicable
Primary location
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
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
Treatment and study plan
Style 410 Silicone-Filled Breast Implants
DeviceBreast Implant Surgery
Primary outcomes
-
Local Complications
Time frame: 10 years
By patient risk of complications occurring in at least 5% of patients in 1 or more cohorts
Secondary outcomes
-
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
Sponsors and collaborators
Lead sponsor
Allergan Medical
Industry
Registry information
Important dates
- Study start
- 2001
- Primary completion
- 2012
- Study completion
- 2012
- First posted
- Jun 4, 2008
- Registry last updated
- Oct 13, 2014
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Safety and Effectiveness of Natrelle(TM) Cohesive Round Silicone-Filled Breast Implants
NCT00689871
Breast Augmentation, Breast Reconstruction
Washington D.C., District of Columbia, United States
View Trial DetailsSafety and Performance of Motiva® Sizers
NCT06274736
Breast Augmentation, Breast Implant; Complications
Coyol, Alajuela Province, Costa Rica
View Trial DetailsSientra Sponsored Silimed Gel-Filled Breast Implant Core Clinical Study
NCT00905645
Breast Augmentation, Breast Reconstruction
Santa Barbara, California, United States
View Trial DetailsA Retrospective Chart Review Study to Evaluate Safety of McGhan Single Lumen Gel-Filled Breast Implants in Patients in China
NCT04261608
Breast Augmentation, Breast Reconstruction
Beijing, Beijing Municipality, China
View Trial Details