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Contrast Medium Volume and Contrast-induced Nephropathy After Percutaneous Coronary Intervention — CONVIN  

Contrast Induced Nephropathy Clinical Trial

Official title:
Contrast Medium Volume and Contrast-induced Nephropathy After Percutaneous Coronary Intervention

Clinical Trial Summary

To investigate the predictive value of the contrast media volume to creatinine clearance (V/CrCl) ratio for the risk of contrast-induced nephropathy (CIN) (i.e., within 48-72 h) and to determine a relatively safe V/CrCl cut-off value to avoid CIN in patients following PCI

Clinical Trial Description

contrast media volume to creatinine clearance (V/CrCl) ratios were obtained from consecutive consenting patients after unselective PCI. Receiver-operator characteristic (ROC) curves were used to identify the optimal sensitivity for the observed range of V/CrCl. The predictive value of V/CrCl for the risk of CIN was assessed using multivariate logistic regression. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01399203
Study type Observational
Source Guangdong General Hospital
Contact Ning Tan, MD
Phone 86-20-83819161
Email tanning100@126.com
Status Recruiting
Phase N/A
Start date January 2010
Completion date January 2012
View Details
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