ACTRN12616000550404尚未招募未知
In patients undergoing diagnostic angiography and percutaneous coronary intervention does reducing TR Band inflation time from 120 minutes to 60 minutes have an effect on bleeding?
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 548
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
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit(—)
- 性别
- All
入选标准
- •1. Any patient undergoing diagnostic coronary angiography or percutaneous coronary intervention;
- •2. Use of a 6F radial artery sheath for access; and
- •3. Intra-procedural administration of 5000 units of heparin.
排除标准
- •1.Concomitant use of other arterial access sites;
- •2.Patient has received thrombolytic therapy up to 12 hours prior to sheath removal;
- •3.Patient has received Gp IIb/IIIa antagonists up to 24 hours prior to sheath removal;
- •4.Estimated glomerular filtration rate (eGFR, based on the Modification of Diet in Renal Disease criteria) less than 30 mL/min per 1.73 m2;
- •5.Patient has received subcutaneous enoxaparin up to 12 hours prior to sheath removal when eGFR is known to be greater than 35mL/min/1.73 m2;
- •6.Patient has received subcutaneous enoxaparin up to 24 hours prior to sheath removal when eGFR is known to be equal to 35mL/min/1.73 m2;
- •7.Patient has received heparin up to 6 hours prior to sheath removal
- •8.Platelet count less than 100 x1^9/L;
- •9.Prothrombin ratio (PR) or international normalized ratio (INR) greater than 1.5 at the time of the procedure;
- •10.Activated partial thromboplastin time (APTT) greater than 45 seconds at the time of the procedure; and/or
- •11.Patient is unable to give informed consent.
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