DRKS00000766招募中4 期
heart rate control after acute myocardial infarction - STEMI
niversität zu Köln0 个研究点目标入组 100 人开始时间: 2011年10月6日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
- 入组人数
- 100
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
- Randomized controlled study
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 one(—)
- 性别
- All
入选标准
- •Acute st-segment elevation myocardial infarction (time between symptom onset and PCI < 6 hours) with successful PCI (TIMI III°)
- •Killip Klassification I, II
- •Written informed consent
- •Resting heart rate = 60 bpm
- •Age above 18 years
- •Mean blood pressure = 65 mmHg
- •Systolic blood pressure > 90mmHg
- •Medication with Heparin (weight adapted), clopidogrel ans aspirin before PCI
- •SO2 > 90%
- •Elevated heart rate (= 60/min)
排除标准
- •Mean blood pressure < 65 mmHg
- •Incomplete PCI success (TIMI < III)
- •Cardiogenic shock
- •Killip Klassification III, IV
- •Symptomatic AV conduction block II°, III°,
- •sinuatrial conduction block (II°, III°)
- •Catecholamin therapy
- •Heart rate < 60/min.
- •Severe peripheral artery disease (Fontaine > IIb)
- •Moderate to severe renal impairment (Serum-creatinin > 2 mg/100ml)
- •Severe liver dysfunction
- •Severe acidosis (pH < 7,2)
- •Known contraindications for Brevibloc (e.g. asthma bronchiale) or known intolerance to Brevibloc
- •Participation in other interventional studies
- •Person related to the sponsor or investigator
- •Subjects who were not eligible for follow-up visits (e.g. due to long distance between study hospital and home adress)
- •Women in whom a pregnancy cannot excluded
- •Missing safe contraception (hormonal or copper spirale)
- •Patients without guidelines recommended therapy previosly to PCI
- •Patients in whom anamnestic the symptom onset was > 6 hours or first laboratory tests indicate (LDH > 280U/I) that the myocardial infarction onset was more than 6 hours and in whom no other reasons for elevated LDH are present.
- •Unsuccessful PCI
- •Symptom onset > 6 hours
研究者
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