Multi-Center Trial Utilizing Low Frequency Ultrasound in the Prevention of Post-Contrast Acute Kidney Injury

Exclusion Criteria

• •Participant is anuric or currently undergoing renal replacement therapy.
• •Participant is currently taking oral nitrates.
• •Participant is undergoing a procedure requiring selective cannulation and injection of contrast into the renal arteries.
• •Participant presented with ST-segment elevation myocardial infarction.
• •Participant has a metal implant in the hip or lumbar spine.
• •Participant received or is anticipated to receive additional intravenous or intraarterial contrast from 7 days prior to cardiac catheterization to 4 days after cardiac catheterization.
• •Addition, discontinuation, or dose change of angiotensin-converting enzyme inhibitor, angiotensin receptor blocker, diuretic, trimethoprim, non-steroidal anti-inflammatory drugs, cimetidine, or metoclopramide with 7 days prior to cardiac catheterization.
• •Participant has a known allergy to contrast medium that cannot be adequately pre-medicated.
• •Participant has new-onset heart failure with New York Heart Association (NYHA) classification of III or IV within 30 days prior to the index procedure.
• •Recent stroke within 90 days prior to the index procedure.
• •Participant has known or suspected active infection at the time of the index procedure.
• •Participant is pregnant and/or breast-feeding or intends to become pregnant during the time of the study.
• •Participant is unwilling or unable to comply with procedures specified in the protocol or has difficulty or inability to return for follow-up visits as specified by the protocol.
• •Participant is known to be incarcerated, mentally incompetent, and/or alcohol or drug abuser.
• •Participant is participating in another investigational drug or medical device study that has not completed primary endpoint(s) evaluation or clinically interferes with the endpoints from this study or subject is planning to participate in such studies prior to the completion of this study.