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Clinical Trial Summary

Indication for use: "The Svelte DES is indicated for improving coronary luminal diameter in patients with symptomatic heart disease, including patients with non-ST elevation MI due to discrete de novo native coronary artery lesions. The treated lesion length should be less than the nominal stent length with a reference vessel diameter of 2.25 mm - 4.00 mm


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03190473
Study type Interventional
Source Svelte Medical Systems, Inc.
Contact
Status Terminated
Phase N/A
Start date January 2, 2018
Completion date March 8, 2023

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