ACTRN12616000025437尚未招募4 期
A randomised controlled trial of Rebuilding the lEft anterior deScending artery for LIMA grafTing with biO-ReabsorbablE scaffolds versus conventional management.
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 70 Years（—）
- 性别
- All
入选标准
- •1. Diffuse LAD disease greater than or equal 50mm in length that is not attractive for surgical revascularisation due to LAD anatomy as judged by a cardiothoracic surgeon.
- •2. Reconstruction of the LAD with BRS is technically feasible as judged by an experienced BRS implanter.
- •3. Preserved antero-apical wall motion
排除标准
- •1. Reconstruction of the LAD with BVS is not technically feasible due to deliverability.
- •2. Significally impaired LV systolic function of the anterior wall without demonstrable ischaemia (FFR <0.80 or moderate to large reversible perfusion defect on ischameia testing in the LAD territory)
- •3. Unable or unlikely to take or tolerate long term DAPT
- •4. Intolerance to Everolimus
- •5. Unlikely to survive the duration of the study due to othe comorbidity
- •6. Advanced renal disease not on haemodialysis (eGFR <30ml/min)
- •7. Within 48 hour of STEMI
- •8. Prior revascularisation of the mid to distal LAD with stents or CABG.
研究者
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