This is a prospective, double-blind, randomized, placebo-controlled study to assess the effects of suramin as a potential treatment option to prevent subjects with AKI from progressing to Kidney Disease Improving Global Outcomes (KDIGO) Stage III or dialysis dependent AKI.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Enrollment
68
University of Arkansas Medical Sciences (UAMS)
Little Rock, Arkansas, United States
California Institute of Renal Research
La Mesa, California, United States
Ronald Reagan UCLA Medical Center
Los Angeles, California, United States
To evaluate and compare the efficacy of a single 3.0 mg/kg infusion of suramin versus placebo in subjects with diuretic unresponsive AKI
The difference between the effect of a 3.0 mg/kg infusion of suramin versus placebo will be based on meeting 2 or more of the composite event endpoints of: peak serum creatinine (Cr) of 6 mg/dL or above from investigational product (IP) infusion through Day or progression to KDIGO Stage III within 72 hours (hr) from IP infusion or death or dialysis from IP infusion through Day 7.
Time frame: 7 days
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Emory University School of Medicine
Atlanta, Georgia, United States
Emory Johns Creek Hospital
Johns Creek, Georgia, United States
University of Kentucky
Lexington, Kentucky, United States
University of Missouri - Dept. of Surgery
Columbia, Missouri, United States
University of New Mexico Health Science Center
Albuquerque, New Mexico, United States
New York-Presbyterian Medical Center of Queens
Flushing, New York, United States
Wake Forest Baptist Medical Center
Winston-Salem, North Carolina, United States
...and 2 more locations