Acute Coronary Syndrome, Coronary Occlusion
Conditions
Keywords
Percutaneous Coronary Intervention, Myocardial Ischemia, Balloon Occlusion, Catheter Lab
Brief summary
The test compound and subject of this clinical trial is the haemoglobin-based oxygen carrier, HBOC-201 (Hemopure). HBOC-201, initially developed as an alternative to red blood cells for surgical patients, has the ability to restore tissue oxygenation in persistently ischemic tissue. The development of this new class of compounds, referred to as oxygen therapeutics, provides an opportunity to test the safety and efficacy of a new approach to management of myocardial ischemia.
Detailed description
Because of their ability to perfuse and deliver oxygen, hemoglobin-based oxygen carriers (HBOC) may be considered in the treatment of several ischemic conditions, such as acute coronary syndromes (ACS). Elective percutaneous intervention (PCI) induces transient myocardial ischemia due to reduction of coronary flow during balloon inflation in the coronary artery, thus simulating in a control setting, the occurrence of an ACS.
Interventions
DRUGHemoglobin Based Oxygen Carrier-201 (HBOC-201, Hemopure)
Pre-oxygenated HBOC-201
Sponsors
Biopure Corporation
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Signed informed consent before initiation of any study-related procedure and agreement to comply with all protocol-specific procedures * Stable angina pectoris (CCS Class 1, 2, 3, 4) or unstable angina (Braundwald class 1-3, B) or documented silent ischemia * Baseline ECG with stable sinus rhythm and no signs of ischemia and with no Q waves, bundle branch block or IV conduction disturbances. * Normal left ventricular wall motion on left ventricular angiogram or on echocardiogram with preserved systolic global LV function * Non-occlusive stenosis, located in the proximal segments of the left anterior descending artery (LAD) (segments 6 and/or 7) and/or circumflex artery (CFX) (segments 11 and/or 12) or right coronary artery (RCA) (segments 1, 2 and/or 3) for which there is clinical indication to percutaneous treatment with coronary stenting * Successful PCI with stenting on the target vessel * Older than 18 years and younger than 80 years of age
Exclusion criteria
* Active ischemia at the initiation of the study procedure * Non-ST segment elevation myocardial infarction * History or ECG evidence of prior MI in the territory supplied by the vessel undergoing PCI, IV conduction defects/baseline ST-segment abnormalities on the surface ECG * Moderate to severe aortic or mitral valve disease * Evidence of LV hypertrophy on the echocardiogram IVS \> 13 and/or PW \> 13mm * Angiographically visible collateral vessels to the target vessel * Hypertension not adequately controlled by anti-hypertensive therapy at the time of study entry (\> 140/100mmHg) * Uncompensated congestive heart failure or signs of pulmonary edema * Significant hemodynamic compromise and/or cardiogenic shock requiring inotropic or pressor support * Contraindications to standard drugs for coronary intervention and coronary heart disease: aspirin, heparin, low molecular weight heparin, clopidogrel, contrast dye * Confirmed pregnancy * Systemic mastocytosis * Hypoxemia (need for mechanical ventilation * Known history of COPD with FEV 1s \< 1.0 liter * Renal impairment: creatinine \> 1.6 mg/dl * Participation in another trial with an investigational drug or device including follow-up period, within the last 30 days before enrollment Additional
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To study the change in left ventricular relaxation indices and pressure-half time and the change in the sum of ST segment deviations compared to baseline. | Duration of the study |
Secondary
| Measure | Time frame |
|---|---|
| LV hemodynamics; change of ST segment; QCA analysis before and after the no-infusion control occlusion and HBOC-201 infusion/occlusion; safety endpoints | Duration of the study |
Countries
Netherlands
Outcome results
None listed