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SUPRAFLEX CRUZ PMCF Study ( rEpic05 ) — Multiflex  

Ischemic Heart Disease Clinical Trial

Official title:
SUPRAFLEX CRUZPost-Market Clinical Follow-up Study

Clinical Trial Summary

Multicenter, prospective, non-randomized, post-market clinical follow-up (PMCF) study to confirm and support the clinical safety and performance of Medical Device Regulations (MDR) with multivessel coronary disease requirements in all the CONSECUTIVE patients treated with (SUPRAFLEX CRUZ).

Clinical Trial Description

The objective of this multicenter, prospective, non-randomized, post-market clinical follow-up (PMCF) study is to confirm and support the clinical safety and performance of the SUPRAFLEX CRUZ in a NON-SELECTED, Real World population under daily clinical practice when used as intended by the manufacturer to meet EU Medical Device regulation requirements for post-market clinical follow-up. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05617599
Study type Observational
Source Fundación EPIC
Contact Bruno Garcia, MD, PhD
Phone 0034932746155
Email brunogb51@gmail.com
Status Recruiting
Phase
Start date May 10, 2023
Completion date October 1, 2025
View Details
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