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Clinical Trial Summary

This was a single-center, prospective, open-label, observational study. Patients with coronary artery disease confirmed by coronary angiography and treated with drug-coated balloon catheter alone for target vessels were enrolled in the Cardiology Department of our hospital in January 2022. The primary endpoint was late lumen loss within 12±3 months after surgery.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05552911
Study type Observational
Source The First Affiliated Hospital with Nanjing Medical University
Contact
Status Recruiting
Phase
Start date January 1, 2022
Completion date December 30, 2023

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