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

CompletedOBSERVATIONAL
Enrollment

70

Participants

Timeline

Start Date

December 14, 2021

Primary Completion Date

May 19, 2022

Study Completion Date

May 19, 2022

Conditions
Venous SystemVenous AccessChemotherapyAntibioticsAntiviralParenteral NutritionTransfusion Blood
Interventions
DEVICE

Central Veinous access devices' insertion

"Medical doctor should complete a questionnaire with medical history or any important clinical data that could help for the selection of the location of the port and catheter placement. The insertion will be planned only by a surgeon, interventional radiologist, or anaesthesiologist in the surgery block.~For the patient with a medical history of PICC line, PAC implantation, Central venous access device of any kind, or clinical risk of veinous compression (cervical or subclavian adenopathy, pelerine syndrome, mediastinal involvement…). An echo Doppler exam of the veinous cervical system is required before surgery. This exam should identify potential thrombosis that required a special treatment. It is important that the surgeon who will perform the device's insertion is aware of any history or risks of veinous thrombosis, stenosis, or phlebitis for the patient to avoid procedure's failure."

Trial Locations (1)

41500

CHR d'Orléans, Orléans

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Eclevar Medtech

INDUSTRY

lead

Perouse Medical

INDUSTRY