Use of JOSTENT Coronary Stent Graft for Coronary Artery Perforations

Service: Trial Number:
052-02
Principal Investigator: Conducted at:
Long Beach Memorial, Saddleback Memorial - Laguna Hills
Currently enrolling additional patients:
Yes
Age Range:
18 years & up

In January, 2001, JOMED received Food and Drug Administration (FDA) Humanitarian Device Excemption (HUD) approval for the sue of the JOSTENT Coronary Stent Graft device. The JOSTENT Coronary Stent Graft device is indicated for use in the treatment of coronary artery perforations in native coronary vessels and/r saphenous vein bypass grafts greater than or equal to 2.75mm in diameter.

MemorialCare Research Center Contact Form

For further information about this study or to express your interest in this study, please fill out and submit this form.
Address
,
 
The email to associate with this registration.