Evaluation of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Early and Evolving Acute Kidney Injury

Kidney Failure, Acute Clinical Trial

— EVOLVE  

Official title:

EValuation Of NGAL in Early and eVolving Acute kidnEy Injury

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00445809
• Other study ID #: BSTE-0401
• Status: Completed
• Phase: N/A
• First received: February 15, 2007
• Last updated: August 3, 2009
• Start date: February 2007
• Est. completion date: April 2009

Study information

• Verified date: August 2009
• Source: Biosite
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

Some patients who undergo cardiovascular surgery requiring cardiopulmonary bypass will develop a kidney injury following their surgery. The purpose of this study is to take a blood sample from patients before they have this type of surgery and then at nine time points after their surgery to test their plasma for a biomarker called NGAL and compare the NGAL levels to their creatinine levels. We hypothesize that NGAL is an earlier marker for kidney injury than creatinine.

Description:

Approximately 350 adults scheduled to undergo cardiac surgery involving the use of cardiopulmonary bypass will be enrolled. Blood samples will be obtained from all patients in the study for future measurement of both plasma NGAL and plasma creatinine levels in the same sample at each of nine time points.

Blood samples for later assessment using the Triage NGAL Test will be processed to plasma at the clinical site, frozen and shipped to Biosite for storage. Testing with the Triage NGAL Test will be conducted at Biosite by trained laboratory personnel. The results of these assessments will be blinded to the medical team during the study and will not impact the medical management of the patient.

The medical team caring for each study patient should obtain clinical laboratory tests per their usual post-operative routine and manage the patient accordingly. Any serum creatinine measurements obtained by the site as part of this routine care both pre-operatively and through Day 10 post-operatively will be recorded as well as any additional post-operative renal insults, the development of oliguria, the need for a nephrology consultation, initiation of dialysis and mortality will also be recorded through Day 10.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 355
• Est. completion date: April 2009
• Est. primary completion date: December 2008
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

4.2.1 Inclusion Criteria

1. Male or female scheduled for cardiovascular surgery (other than cardiac transplant) requiring cardiopulmonary bypass

2. 18 years of age or older

i. The first approximately 150 to200 patients enrolled must have:

• A Prediction of Acute Renal Failure Score = 5 (see Reference 18 and Appendix B)

ii. The subsequent patients enrolled must have one or more of the following risk factors for post-bypass renal injury:

• Age > 70;

• Pre-operative creatinine > 1.4 mg/dL;

• NYHA Class 3 or 4 heart failure or left ventricular ejection fraction < 35%;

• Insulin-dependent diabetes mellitus;

• Undergoing cardiac valve surgery;

• History of previous cardiac surgery.

Exclusion Criteria:

• Age < 18 years

• Inability to obtain Informed Consent from patient or representative

• Prisoners or other institutionalized or vulnerable individuals

• Participation in an interventional clinical study within the previous 30 days

• History of previous renal transplantation

• Stage 5 chronic kidney disease (estimated GRF<15 mL/min/1.73m2) (See Appendix C)

• Known or suspected ongoing pre-operative acute renal failure due to any cause, including pre-renal, intrinsic renal or post-renal (obstructive) etiologies (as evidenced by increasing serum creatinines or oliguria pre-operatively)

• Already receiving dialysis, in imminent need of dialysis or considered highly likely to need dialysis in the immediate post-operative period for fluid management

• Any known or suspected renal ischemic insult(such as cardiac arrest)or nephrotoxic insult(other than intravascular contrast procedure) during the 48 hours prior to surgery

• Known or suspected infection with human immunodeficiency virus (HIV), hepatitis C virus (HCV)infection, hepatitis B virus (HBV) infection or other infectious hepatitis

• Pre-operative hematocrit <25%, recent blood transfusions have been administered to maintain hematocrit >25% or any other contraindication to obtaining the study-specified blood samples

• Undergoing cardiac transplantation

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Acute Kidney Injury
• Kidney Failure, Acute
• Renal Insufficiency

Locations

Country	Name	City	State
Canada	University of British Columbia	Vancouver	British Columbia
United States	St. Peters Healthcare	Albany	New York
United States	Beth Israel Deaconess Medical Center	Boston	Massachusetts
United States	Massachusetts General Hospital	Boston	Massachusetts
United States	New York Methodist	Brooklyn	New York
United States	Cleveland Clinic Foundation	Cleveland	Ohio
United States	St. Anthony's Central Hospital	Denver	Colorado
United States	University of Texas, Houston	Houston	Texas
United States	University of Pittsburgh	Pittsburgh	Pennsylvania
United States	Maine Medical Center	Portland	Maine
United States	George Washington University	Washington	District of Columbia

Sponsors (1)

Lead Sponsor	Collaborator
Biosite

Countries where clinical trial is conducted

United States,  Canada,