AVERT™ Clinical Trial for Contrast Media Volume Reduction and Incidence of CIN

Overview

About this study

The Osprey Medical AVERT System is indicated to reduce contrast media (CM) exposure to the kidneys during percutaneous coronary procedures thereby reducing the risk of contrast induced nephropathy (CIN).

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

The subject is a candidate for a therapeutic percutaneous coronary intervention (PCI) procedure.
The subject has documented chronic kidney disease (CKD)

Exclusion Criteria:

Subject is in acute renal failure
Assessment of ventricular function that cannot be accomplished without the use of the CM.
Subject has acute STEMI within 72 hours prior to planned PCI procedure, or is currently having an acute STEMI.
Subject is unable to undergo peri-procedural hydration.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location	Status
Rochester, Minn. Mayo Clinic principal investigator Patricia Best, M.D.	Closed for enrollment

Mayo Clinic Location

Status

Rochester, Minn.

Mayo Clinic principal investigator

Patricia Best, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Clinical Trials