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NOT YET RECRUITING
NCT07383012

LTFU of PCL Breast Scaffolds Used in 2021-BRV-004

Sponsor: BellaSeno Pty Ltd

View on ClinicalTrials.gov

Summary

The objective of this study is to assess the long-term safety and performance of the PCL Breast Scaffold in women who previously underwent breast silicone implant revision and received the PCL Breast Scaffold combined with autologous fat grafting (AFG) in the 2021-BRV-004 clinical trial (ClinicalTrials.gov ID: NCT05437757). In addition, this study will investigate the suitability of mammography in the subset of patients that fall into the national breast screening age category - individuals aged 40 years and older. The main questions this study aims to answer are: * "Is the PCL Breast Scaffold combined with autologous fat grafting a safe and effective method of soft-tissue reconstruction following breast implant revision?" * "Is mammography a suitable follow-up screening and diagnostic tool for patients implanted with the PCL Breast Scaffold?" Participants will attend annual follow-up visits from 3 to 5 years after PCL Breast Scaffold implantation for clinical assessments and patient-reported outcome questionnaires.

Official title: Long-term Follow-up Study to Evaluate the Long-term Safety and Performance of PCL Breast Scaffolds Used for Breast Implant Revision Surgery in 2021-BRV-004

Key Details

Gender

FEMALE

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

19

Start Date

2026-02

Completion Date

2029-02

Last Updated

2026-02-03

Healthy Volunteers

No

Locations (1)

Royal Brisbane and Women's Hospital (RBWH), Herston Biofabrication Institute (HBI)

Brisbane, Queensland, Australia, Australia