DuraSorb® in Prosthetic Breast Reconstruction

Status Active, not recruiting

Clinical Trial Summary

This study compares outcomes of prospective mesh-based breast reconstructions to historical control breast reconstructions with no mesh.

Clinical Trial Description

Plastic surgeons have a variety of biologic and synthetic mesh available for use. However, no mesh has adequately evaluated safety and effectiveness for FDA approval or clearance for use in breast reconstruction. Therefore, no mesh is an appropriate comparator for a randomized clinical study. This multi-center, prospective, clinical study with matched historical controls of total submuscular 2-stage breast reconstructions with no mesh will evaluate the safety and effectiveness of DuraSorb® monofilament surgical mesh when implanted in subjects undergoing 2-stage breast reconstruction. Women scheduled for mastectomy and immediate 2-stage breast reconstruction will sign informed consent and satisfy eligibility criteria prior to the first stage of surgery and DuraSorb® implantation. Maximum study follow-up is through one year after definitive reconstruction. ;

Study Design

Related Conditions & MeSH terms

Breast Reconstruction

Clinical Trial Details

NCT number	NCT04646057
Study type	Interventional
Source	Surgical Innovation Associates, Inc.
Contact
Status	Active, not recruiting
Phase	N/A
Start date	January 15, 2021
Completion date	December 2024

View Details

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