TOSCA-2: Angioplasty and Heart Stents to Treat Individuals With an Occluded Artery Following a Heart Attack
Study Details
Study Description
Brief Summary
The purpose of this study is to evaluate arterial patency and left ventricular ejection fraction by examining angiographic data one year following a heart attack and treatment with late revascularization.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 4 |
Detailed Description
BACKGROUND:
The Occluded Artery Trial (OAT) is an international study with 3200 participants. Its goal is to determine if delayed mechanical reperfusion by means of percutaneous transluminal coronary angioplasty (PTCA) and stenting reduces death, heart attacks, and hospitalization in individuals with New York Heart Association (NYHA) Class IV heart failure and a persistently occluded infarct-related artery (IRA) 3 to 28 days following a heart attack. While left ventricular (LV) function improvement has been suggested as a benefit of late reperfusion, solid evidence to support this claim is lacking. Furthermore, while stenting has reduced reocclusion rates after total occlusion PTCA, the reocclusion rate after a recent heart attack is unknown.
DESIGN NARRATIVE:
This study is a substudy of OAT and will enroll 380 participants. The primary aims of the study include the following: 1) to compare long-term patency rates between the two treatment groups (conventional medical therapy or PTCA and stenting) by means of follow-up coronary angiography one year after enrollment; and 2) to compare the change in global LV ejection fraction between the two treatment groups utilizing baseline and follow-up contrast LV angiograms. Secondary aims include the following: 1) comparison of regional wall motion and LV volumes; 2) study of the effect of reocclusion and spontaneous recanalization on LV function; and 3) study of the effect of duration of occlusion on changes in LV function after Percutaneous Coronary Intervention (PCI). The substudy will be conducted at 21 OAT study sites. The Substudy Coordinating Center (SCC) is at the University of Alberta in Edmonton, Canada. The Data Coordinating Center (DCC) is at the Maryland Medical Research Institute, which is the DCC for the OAT study. The Angiographic Core Laboratory is at the University of British Columbia.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: 1 PCI with stenting of the occluded culprit infarct-related artery plus optimal medical therapy |
Device: PCI with stenting
PCI with stenting of the occluded culprit infarct-related artery
Behavioral: Optimal Medical Therapy
Participants will receive optimal medical therapy.
|
| Active Comparator: 2 Optimal medical therapy alone without PCI of the occluded culprit artery |
Behavioral: Optimal Medical Therapy
Participants will receive optimal medical therapy.
|
Outcome Measures
Primary Outcome Measures
- LV ejection fraction [1 year]
- Infarct-related artery patency (measured by contrast LV and coronary angiography) [1 year]
Secondary Outcome Measures
- Comparison of regional wall motion and LV volumes [1 year]
- Effect of reocclusion and spontaneous recanalization on LV function [1 year]
- Effect of duration of occlusion on changes in LV function after PCI [1 year]
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Has experienced a heart attack 3 to 28 days prior to study entry
-
Has a persistently occluded IRA
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University Health Network - Toronto General Hospital | Toronto | Ontario | Canada |
Sponsors and Collaborators
- University Health Network, Toronto
- National Heart, Lung, and Blood Institute (NHLBI)
Investigators
- Study Chair: Vladimir Dzavik, MD, University Health Network - Toronto General Hospital
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 989
- R01HL067683