Clinical Trials Directory

Trials / Completed

CompletedNCT01256502

The SERI® Surgical Scaffold Use in Reconstruction Post Market Study for Tissue Support and Repair in Breast Reconstruction Surgery

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
160 (actual)
Sponsor
Sofregen Medical, Inc. · Industry
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to obtain clinical experience with the use of SERI® Surgical Scaffold for tissue support and repair in breast reconstruction.

Conditions

Interventions

TypeNameDescription
DEVICESERI® Surgical ScaffoldBreast reconstruction surgery

Timeline

Start date
2010-10-01
Primary completion
2012-10-01
Completion
2014-04-01
First posted
2010-12-08
Last updated
2017-11-06
Results posted
2014-05-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01256502. Inclusion in this directory is not an endorsement.