The objective of this study is to prospectively monitor the incidence of adverse drug reactions, specifically NSF during routine use of gadoversetamide in a large number of patients with moderate renal insufficiency (eGFR 30-59) and severe renal insufficiency or end-stage renal disease requiring dialysis (eGFR \<30).
Study Type
OBSERVATIONAL
Radiology Consultants, Inc.
Youngstown, Ohio, United States
The primary outcome measure will be the diagnosis of NSF based on clinical assessments and patient telephone calls through 24 months of follow-up.
Time frame: 1, 3, 6, 12, 18 and 24 months
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