Post-Market Observation Study of Intra-renal Drug Delivery (PROVIDE)

Terminated

• Conditions: Acute Kidney Injury; Renal Failure Chronic Contrast Induced; Chronic Kidney Disease; Acute Renal Failure
• Interventions: Device: Benephit catheter for Targeted Renal Therapy

• Registration Number: NCT01064895
• Lead Sponsor: Angiodynamics, Inc.

Brief Summary

This is a prospective, observational, multi-center study with consecutive enrollment. Up to 500 patients will be enrolled. All (consecutive) adult patients in whom one or more components of the Benephit Infusion System are planned to be used at participating sites are eligible for enrollment. The objective of this post-marketing surveillance study is to collect clinical usage patterns of the Benephit Infusion Systems. As a result, AngioDynamics will be able to (1) Better understand and quantify usage patterns including patient characteristics, adjunctive procedures, and infusion agents, (2) Collect user-interface information and overall customer satisfaction, and (3) Monitor post-marketing device performance and safety for ISO quality adherence.

Detailed Description

Acute kidney injury, or AKI, is a rapid decline in renal function characterized by a decrease in urine output and/or an increase in serum creatinine (Cr), and is associated with worsened clinical outcomes and increased healthcare costs. AKI may be caused by numerous factors including interruptions or perturbations of renal blood flow or toxins, and often these factors are extra-renal in origin. AKI diagnoses in hospitalized patients are over one million per year and are projected to continue to grow, due largely to the aging population and increasing numbers of medical and invasive procedures performed on the elderly and the ever-increasing prevalence of diabetes mellitus and its medical complications, as well as increasing awareness within the medical community.

Treatment options for established acute kidney injury are limited and consist mainly of fluid and electrolyte balance (diuretics and/or IV fluids) supportive care up until the point that dialysis or other renal replacement therapy (RRT) is required. Despite the advent of newer drugs, more sophisticated RRT equipment, and increased awareness of the problem, little has changed relative to patient outcomes, which remain poor. Similarly, limited options exist in patients with known risk factors for AKI to prevent its development due to iatrogenic causes (e.g., major surgery, exposure to contrast media).

Targeted Renal Therapy allows for direct delivery of therapeutically relevant doses of various pharmacological agents directly to the renal bed, potentially reducing dose limiting side effects of traditional IV therapy. With Targeted Renal Therapy, or TRT, the kidney can metabolize, conjugate, and/or clear a substantial portion of many agents immediately (known as the "renal first-pass" effect), reducing the amount that is returned to the systemic circulation via the renal veins, thus potentially reducing untoward side effects. While the existence of a renal first-pass effect has been hypothesized in the medical literature for some time, it has not been possible to take clinical advantage of this important physiological function prior to the advent of AngioDynamics' TRT. Thus, TRT has the potential to offer an additional preventative or treatment opportunity in those patients at risk for AKI, or with established AKI, respectively.

Study Timeline

• Study Start: 2010-02
• Study First Submitted: 2010-02-05
• Study First Submitted QC: 2010-02-05
• Study First Posted: 2010-02-09
• Primary Completion: 2011-12
• Study Completion: 2011-12
• Status Verified: 2016-11
• Last Update Submitted: 2016-11-07
• Last Update Posted: 2016-11-08

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Physician-determined need for Benephit device/Targeted Renal Therapy
• Age >=18 years
• Ability to provide written informed consent

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Exclusion Criteria

• Patients who are participating in another IRB approved research study that precludes simultaneous enrollment

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Active Cohort	Benephit catheter for Targeted Renal Therapy	Patients receiving the Benephit device and targeted renal therapy.

Trial Locations

Locations (15)

St. John Hospital & Medical Center; 🇺🇸 Detroit, Michigan, United States

Baptist Cardiac & Vascular Institute; 🇺🇸 Miami, Florida, United States

HealthwoRx South Florida Research Solutions; 🇺🇸 Miramar, Florida, United States

King's Daughters Medical Center; 🇺🇸 Ashland, Kentucky, United States

Cardiology Associates of NW Indiana; 🇺🇸 Munster, Indiana, United States

Graves Gilbert Clinic; 🇺🇸 Bowling Green, Kentucky, United States

Western Kentucky Heart and Lung; 🇺🇸 Bowling Green, Kentucky, United States

Bingham Memorial Hospital; 🇺🇸 Blackfoot, Idaho, United States

Sahetya Medical Institute; 🇺🇸 Bowling Green, Kentucky, United States

Midwest Cardiovascular Research Foundation; 🇺🇸 Davenport, Iowa, United States

St. Joseph Health Center; 🇺🇸 St. Charles, Missouri, United States

University of Maryland Medical Center; 🇺🇸 Baltimore, Maryland, United States

Chambersburg Hospital; 🇺🇸 Chambersburg, Pennsylvania, United States

Utah Cardiology PC; 🇺🇸 Layton, Utah, United States

Virginia Commonwealth University Medical Center; 🇺🇸 Richmond, Virginia, United States