Initial Experience With the AngioVac Venous Drainage Cannula

AngioDynamics

Status: Completed

Conditions: Heart Disease

Treatments: Device: AngioVac

Study type: Observational

Funder types: Industry

Identifiers

NCT02775565

PV-AV400

Details and patient eligibility

About

This is a retrospective, record-based study of approximately 100 patients across up to 12 centers within the United States. All patients who have been treated with the AngioVac Venous Drainage Cannula and the Extracorporeal Circuit will be considered for study participation. Eligible subject must meet all of the inclusion criteria and none of the exclusion criteria to be considered enrolled in the study. The purpose of the study is to describe initial experience with the AngioVac Venous Drainage Cannula and the Extracorporeal Circuit.

Enrollment: 51 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Consecutive patients treated at each study site between February 1, 2013 and February 28, 2015 will be included.

Exclusion criteria

• Patients treated with the AngioVac venous drainage system outside of those dates.