Sientra Post-Approval Study
This study is currently recruiting participants.
Verified July 2012 by Sientra, Inc.
Information provided by (Responsible Party):
First received: July 10, 2012
Last updated: July 11, 2012
Last verified: July 2012
This is a ten-year postapproval study to evaluate the long-term clinical performance of Sientra Silicone Gel Breast Implants under general conditions of use in the postmarket environment.
|Study Design:||Observational Model: Cohort
Time Perspective: Prospective
|Official Title:||U.S. Postapproval Study of Sientra Silicone Gel Breast Implants|
Resource links provided by NLM:
Further study details as provided by Sientra, Inc.:
|Study Start Date:||April 2012|
|Estimated Study Completion Date:||December 2023|
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01639053
|Contact: Sientra, Inc|
|United States, California|
|Santa Barbara, California, United States, 93117|
|Contact: Sientra, Inc 888-708-0808|
Sponsors and Collaborators
|Study Director:||Sientra, Inc.||Sponsor GmbH|