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Clinical Trial Summary

This is a single-center, prospective, controlled and diagnostic clinical trial which will enroll 30 patients scheduled for coronary angiography in China.Patients will receive contrast-enhanced cardiac magnetic resonance with polysaccharide superparamagnetic iron oxide nanoparticle before percutaneous coronary angiography.In order to evaluate the safety of polysaccharide superparamagnetic iron oxide nanoparticle, patients will detect iron levels in peripheral and tissue before and after the examination.The main indicators of the study are the degree of coronary artery stenosis and the stability of coronary atherosclerotic plaque assessed by contrast-enhanced cardiac magnetic resonance with polysaccharide superparamagnetic iron oxide nanoparticle.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05032937
Study type Interventional
Source The First Affiliated Hospital with Nanjing Medical University
Contact Chunjian Li, Dr, PhD
Phone +86-13701465229
Email [email protected]
Status Not yet recruiting
Phase Phase 1
Start date September 1, 2021
Completion date July 1, 2022

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