Chronic ischemic heart failure
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Patients who received VCF1 in the investigator-initiated phase 1 study (MTC001-2012) and who have consented to this observational study by the end of study participation (52 weeks). 2)Patients who are able to obtain written consent in person.
Exclusion criteria
Exclusion criteria: 1)Patients who withdrew consent after receiving VCF1 in the investigator-initiated phase I study (MTC001-2012) 2)Patients deemed ineligible by the Principal Investigator or Sub investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Occurrence of major cardiovascular events *: Major cardiovascular events: death, myocardial infarction, stroke, hospitalization/prolonged hospitalization due to worsening heart failure, cardiac perforation, cardiac tamponade, sustained ventricular tachycardia (>30 seconds or hemodynamic collapse)/ventricular fibrillation among serious adverse events | — |
Contacts
University of Tsukuba Hospital