COBRA SHIELD OCT Study

NATerminatedINTERVENTIONAL
Enrollment

8

Participants

Timeline

Start Date

June 30, 2014

Primary Completion Date

June 30, 2015

Study Completion Date

June 30, 2015

Conditions
Stable Angina
Interventions
DRUG

Aspirin

75-325 mg q.d. aspirin until study completion (recommended indefinitely for stent patients)

DEVICE

Resolute Integrity DES

Resolute Integrity DES

DEVICE

COBRA PzF

DRUG

DAPT

At the discretion of the investigator as to which DAPT is administered (per local practice)

Trial Locations (2)

20520

Heart Center, Turku University Hospital, Turku

28500

Satakunta Central Hospital, Pori

Sponsors
All Listed Sponsors
collaborator

ClinLogix. LLC

INDUSTRY

lead

CeloNova BioSciences, Inc.

INDUSTRY