Clinical Trial: A Retrospective, Observational, Monocenter, Study to Describe the Utilization and Overall Safety and Performance of POLYSITE�/SEESITE� Implantable Ports

Study Status: Completed
Recruit Status: Completed
Study Type: Observational




Official Title: A Retrospective, Observational, Monocenter, Study to Describe the Utilization and Overall Safety and Performance of POLYSITE�/SEESITE� Implantable Ports

Brief Summary: This study is a retrospective, observational, monocenter case series. The purpose of this study is to collect clinical data to describe the use of POLYSITE� and SEESITE� devices and verify overall safety and performance. This study is part of the Post-Market Clinical Follow-up (PMCF) activities of the PEROUSE MEDICAL manufacturer.
The primary data source for this study was patient's medical records from a French Hospital. The study population was defined as all patients who did receive POLYSITE� and SEESITE�. Data from a minimum of 50 patients were planned for the statistical review.