Patients with stable myocardial ischemia who undergo elective PCI.
Conditions
Interventions
Control: Subjects who do not undergo any pre-treatment before PCI.
RIPC: Subjects who undergo RIPC pre-treatment induced by three 5-minute inflations of a blood pressure cuff to 200mmHg around the
Sponsors
Department of Cardiovascular Medicine, Okayama Univesity Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Silent myocardial ischemia or stable angina pectoris patient. 2. Over 20 years old patient.
Exclusion criteria
Exclusion criteria: 1. Acute coronary syndrome patient undergoing emergency PCI. 2. Patient corresponded contra- indication of intravenous Nicorandil administration. 3. Patient undergoing PCI to chronic total occlusion lesion or patients undergoing PCI with rotablator. 4. Diabetes patient treated with glibenclamide. 5. Patient with AV shunt on the arms 6. Patient whose prognosis is regarded as less than 12 months. 7. Patient considered to be improper to this study by attending doctor.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The ratio of patients with acute myocardial infarction associated with PCI employing the 2007 universal definition by the joint ESC-AHA-ACC-WHF task force. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Ischemic event during PCI and 8 months MACE after PCI procedure 2. safety of RIPC and Nicorandil | — |
Countries
Japan
Contacts
Public ContactKunihisa Kohno
Okayama Univesity Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Department of Cardiovascular Medicine
Outcome results
None listed