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Clinical Trial Summary

The IVL-Dragon Registry was a multicenter study that enrolled consecutive patients with stent underexpansion treated with IVL in high-volume PCI centers. The primary efficacy endpoint was clinical success, defined as a reduction of stent underexpansion to <30% with no evidence of in-hospital device-oriented composite end point (DOCE) (defined as a composite of cardiac death, target lesion revascularization, and target vessel myocardial infarction).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05112250
Study type Observational [Patient Registry]
Source Medical University of Silesia
Contact
Status Completed
Phase
Start date November 1, 2019
Completion date April 1, 2021

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