Background and purpose: Contrast-induced nephropathy (CIN) is an important complication of angiographic procedures. This study aimed to evaluate the effect of a single dose of ezetimibe on the incidence of CIN and changes in renal function indices following exposure to contrast media.
Materials and methods: This double-blind clinical trial was conducted in 144 patients undergoing coronary angiography, who were randomly assigned to receive ezetimibe (n = 73) or placebo (n = 71). Serum creatinine and glomerular filtration rate (GFR) were measured before the intervention and 48-72 hours after the intervention. The primary outcome was the incidence of CIN, defined as an increase in serum creatinine of at least 0.3 mg/dL or at least 1.5 times the baseline value within 48-72 hours of contrast exposure. CIN incidence was compared using Fisher's exact test, and the effect size was expressed as the risk ratio (RR) with a 95% confidence interval (CI). Analysis of covariance (ANCOVA) was used to compare post-intervention serum creatinine and GFR between the groups after adjustment for baseline values.
Results: CIN occurred in one patient (1.4%) in the ezetimibe group and three patients (4.2%) in the placebo group. Although CIN was less frequent in the ezetimibe group, the difference was not statistically significant (Fisher's exact test, P = 0.363; RR = 0.324; 95% CI: 0.035–3.040). After adjustment for baseline creatinine, post-intervention creatinine was significantly lower in the ezetimibe group (F = 7.349, P = 0.008, partial η² = 0.050). Similarly, after adjustment for baseline GFR, post-intervention GFR was significantly higher in the ezetimibe group (F = 14.348, P < 0.001, partial η² = 0.092).
Conclusion: In this study, ezetimibe was associated with significantly more favourable changes in renal function indices, including serum creatinine and GFR, after adjustment for baseline values. These findings suggest a potential beneficial effect of ezetimibe on renal function following contrast exposure; however, further studies are needed to confirm this effect.
(Clinical Trials Registry Number: IRCT20250702066339N1)