Clinical Trials Directory

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UnknownNCT02890160

A Trial of Firesorb in Patients With Coronary Artery Disease: FUTURE-II

A Randomized Trial of the Firesorb Sirolimus Target Eluting Bioresorbable Vascular Scaffold in Patients With Coronary Artery Disease: FUTURE-II

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
430 (estimated)
Sponsor
Shanghai MicroPort Medical (Group) Co., Ltd. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The FUTURE-II study is a confirmative clinical trial for Sirolimus Target Eluting Bioresorbable Vascular Scaffold (Firesorb) after the feasibility and safety of the device has been preliminary confirmed in a small-scale First-in-Man clinical trial.

Detailed description

This study is a prospective, multicenter, single-blind, randomized controlled trial in patients with coronary artery disease caused by up to two de novo native coronary artery lesions in separate epicardial vessels. The goal is to evaluate the safety and effectiveness of Firesorb to support the approval of the Chinese Food and Drug Administration (CFDA) for this product. The Abbott's XIENCE Everolimus-eluting Coronary Stent System is selected as the control device. 430 subjects will be recruited. All subjects will be 1:1 randomly assigned to experimental group and control group. All subjects will undergo clinical follow-up at 1-month, 6-month, 1-year, 2-year, 3-year, 4-year and 5-year post-index procedure. All subjects will undergo angiographic follow-up at 1-year post-index procedure; of which 3-5 centers will be specified as a subgroup to complete OCT follow-up (n=80, 40 each in test and control group).

Conditions

Interventions

TypeNameDescription
DEVICEFiresorbSirolimus Target Eluting Bioresorbable Vascular Scaffold
DEVICEXIENCEEverolimus Eluting Coronary Stent System

Timeline

Start date
2017-08-24
Primary completion
2020-10-31
Completion
2024-10-01
First posted
2016-09-07
Last updated
2023-10-25

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02890160. Inclusion in this directory is not an endorsement.