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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00774137
Other study ID # 0603001221
Secondary ID R01HL085757
Status Completed
Phase
First received
Last updated
Start date April 2007
Est. completion date February 2014

Study information

Verified date April 2020
Source Yale University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

People who undergo coronary artery bypass grafting (CABG) or heart valve surgery may experience acute kidney injury (AKI) after their surgery. Current medical tests cannot identify AKI until approximately 48 hours after it occurs. This study will examine three new biomarkers in blood and urine that may provide a more effective and faster way of predicting AKI in people who undergo CABG or heart valve surgery.


Description:

AKI, which is indicated by a sudden change in serum creatinine levels, is a serious complication that can occur after a patient undergoes CABG or heart valve surgery. People who experience AKI after heart surgery may be at increased risk for post-operative complications, including long-term kidney failure or heart damage. AKI is currently identified by testing serum creatinine levels in the blood, which is the traditional marker of kidney function. However, serum creatinine levels can be affected by other non-kidney-related factors and may not positively identify AKI until 48 hours after it begins. This study will examine three new biomarkers found in urine and blood—urine interleukin 18 (IL-18), neutrophil gelatinase-associated lipocalin (NGAL), and cystatin C—that may be able to predict AKI more effectively and faster than serum creatinine levels. In addition, study researchers will also determine if changes in these biomarkers can predict the severity of AKI more successfully than serum creatinine tests.

This study will enroll people undergoing CABG or heart valve surgery at Yale-New Haven Hospital. Before the surgery and once a day for 5 days after the surgery, blood and urine collection will occur. Study researchers will also review participants' medical records. Twelve months after hospital discharge, participants will return to the clinic for a follow-up visit for repeat blood and urine collection and to complete questionnaires. A portion of blood will be saved for future genetic testing; this is optional.


Recruitment information / eligibility

Status Completed
Enrollment 1550
Est. completion date February 2014
Est. primary completion date February 2013
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria for Adults: (must have at least one of the following)

- Emergent surgery

- Pre-existing kidney impairment (baseline serum creatinine greater than 2 mg/dL)

- Ejection fraction less than 35%

- At least 70 years old

- Diabetes mellitus

- Combined CABG and valve surgery

- Repeat CABG or valve surgery

Exclusion Criteria for Adults:

- Pre-operative acute kidney injury

- Enrolled in a conflicting research study

- Prior kidney transplantation

- Baseline serum creatinine level greater than 4.5 mg/dL

- Nephrotoxic drugs administered pre-operatively

- Surgery for only left ventricular assist device

Inclusion Criteria for Children:

- Undergoing open heart surgery

Exclusion Criteria for Children:

- Pre-existing acute kidney failure (greater than 50% decline in creatinine clearance)

Study Design


Locations

Country Name City State
Canada London Health Sciences Centre London Ontario
Canada Montreal Children's Hospital at McGill University Health Centre Montreal Quebec
United States University of Chicago School of Medicine Chicago Illinois
United States Cincinnati Children's Hospital Medical Center Cincinnati Ohio
United States Danbury Hospital Danbury Connecticut
United States University of Colorado Health Sciences Center Denver Colorado
United States Duke Clinical Research Institute Durham North Carolina
United States Yale University School of Medicine New Haven Connecticut

Sponsors (2)

Lead Sponsor Collaborator
Yale University National Heart, Lung, and Blood Institute (NHLBI)

Countries where clinical trial is conducted

United States,  Canada, 

References & Publications (5)

Li S, Krawczeski CD, Zappitelli M, Devarajan P, Thiessen-Philbrook H, Coca SG, Kim RW, Parikh CR; TRIBE-AKI Consortium. Incidence, risk factors, and outcomes of acute kidney injury after pediatric cardiac surgery: a prospective multicenter study. Crit Car — View Citation

Parikh CR, Coca SG, Thiessen-Philbrook H, Shlipak MG, Koyner JL, Wang Z, Edelstein CL, Devarajan P, Patel UD, Zappitelli M, Krawczeski CD, Passik CS, Swaminathan M, Garg AX; TRIBE-AKI Consortium. Postoperative biomarkers predict acute kidney injury and po — View Citation

Parikh CR, Devarajan P, Zappitelli M, Sint K, Thiessen-Philbrook H, Li S, Kim RW, Koyner JL, Coca SG, Edelstein CL, Shlipak MG, Garg AX, Krawczeski CD; TRIBE-AKI Consortium. Postoperative biomarkers predict acute kidney injury and poor outcomes after pedi — View Citation

Shlipak MG, Coca SG, Wang Z, Devarajan P, Koyner JL, Patel UD, Thiessen-Philbrook H, Garg AX, Parikh CR; TRIBE-AKI Consortium. Presurgical serum cystatin C and risk of acute kidney injury after cardiac surgery. Am J Kidney Dis. 2011 Sep;58(3):366-73. doi: — View Citation

Zappitelli M, Krawczeski CD, Devarajan P, Wang Z, Sint K, Thiessen-Philbrook H, Li S, Bennett MR, Ma Q, Shlipak MG, Garg AX, Parikh CR; TRIBE-AKI consortium. Early postoperative serum cystatin C predicts severe acute kidney injury following pediatric card — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in serum creatinine levels (absolute and percentage) Measured in the 1 week after surgery
Secondary Doubling of serum creatinine, use of dialysis, or death Measured during hospitalization
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