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Clinical Trial Summary

The investigators aimed to compare the image quality and diagnostic performance of DECTPA using lower concentration iodine contrast materials and using normal concentration iodine contrast materials in the evaluation of suspected pulmonary embolism.


Clinical Trial Description

All patients met the inclusion and exclusion criteria will be given written informed consensus. The enrolled patients will randomly receive one of the three injection protocols: A: 30mL Iomeprol (Iomeron 300, Bracco Imaging, Milano, Italia) injected at a flow rate of 4mL/s; B: 50mL Iomeprol (Iomeron 300, Bracco Imaging, Milano, Italia) injected at a flow rate of 4mL/s; C: 50mL Ioversol (Ioversol 350, Hengrui, Jiansun, China) injected at a flow rate of 4mL/s. A and B groups are both lower concentration iodine contrast material groups, with different total iodine loads. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06212882
Study type Observational
Source Wuxi People's Hospital
Contact Xiangming Fang, Doctor
Phone +86 15295557003
Email mengxp0711@163.com
Status Recruiting
Phase
Start date September 1, 2023
Completion date June 2025

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