Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT02222116

OCT Study of the MGuard Prime Stent in Patients With Heart Attacks

OCT Study of the MGuard Prime Embolic Protection Stent in Patients With Acute ST-segment Elevation Myocardial Infarction

Status
Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
InspireMD · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The objective is to demonstrate that the Flow Area within a blocked coronary vessel as assessed by OCT is greater with the MGuard Prime stent compared to non-mesh control stent (BMS/DES) in subjects undergoing primary PCI for ST-segment elevation MI. The study hypothesis is that end of procedure flow area is greater with the MGuard Prime compared with stenting with a non-mesh DES or BMS.

Conditions

Interventions

TypeNameDescription
DEVICEMGuard Prime
DEVICEControl BMS DES

Timeline

Start date
2015-10-01
Primary completion
2015-11-01
Completion
2016-01-01
First posted
2014-08-21
Last updated
2015-03-31

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT02222116. Inclusion in this directory is not an endorsement.