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Clinical Trial Summary

To compare MiStent to either the Xience or Promus stents.with the primary objective being to assess the safety and efficacy of the MiStent in a patient population requiring revascularization of de novo obstructive lesions of coronary arteries in patients with stable and unstable coronary artery disease (CAD) including non ST-Elevation Myocardial Infarction (NSTEMI)


Clinical Trial Description

The CRYSTAL study is a prospective, multi-center, randomized (1:1), single-blinded and controlled, investigational device exemption trial to test the non-inferiority of MiStent to commercially available "everolimus" drug eluting stents (Xience and Promus stents).

Patients with coronary artery disease (CAD) that qualify for percutaneous coronary intervention (PCI) with stenting will be screened per the protocol inclusion and exclusion criteria. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03423511
Study type Interventional
Source Micell Technologies
Contact Jeffrey Mifek
Phone 919-313-2102
Email jmifek@micell.com
Status Not yet recruiting
Phase N/A
Start date June 1, 2018
Completion date June 1, 2024

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