DRKS00016852已完成不适用
Berlin Longterm Observation of Vascular Events - Pilot study - BeLOVE - Pilot study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 2,248
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 one(—)
- 性别
- All
入选标准
- •provision of signed and dated informed consent form
- •2)declared willingness to take part in study procedures and to be contacted again for further
- •follow-up examinations
- •3)persons of any sex and gender, aged 18 years or above at the time of acute event or study
- •4)general health status is acceptable for participation in a study
- •5)clinical diagnosis of one or more of the following diseases:
- •A) acute heart failure (trigger event), defined by:
- •i) dyspnoe NYHA IIIb or IV and NTproBNP = 300 pg/nl OR
- •MRproANP = 120 pmol/l, AND
- •ii)evidence of pitting peripheral edema or radiological or clinical signs of
- •of pulmonary congestion, AND
- •iii)Need for i.v.-administration or dose escalation of diuretic therapie
- •equivalent to furosemid 40 mg or torasemid of 10 mg.
- •B) acute coronary syndrome (trigger event), defined by:
- •i) acute cardiac chest pain, or angina equivalent consistent with moderate to high-
- •risk unstable angina or myocardial infarction, lasting more than 10 minutes
- •duration during72 hours before invasive examination, AND
- •ii) evidence for ACS requiring catheterization documented by
- •(1)elevated enzymes (CK-MB or hs-troponin i/T >99th percentile or in-
- •/decrease) AND/OR
- •(2)ECG with ST-depression >1mm in 2 or more contiguous leads after the
- •J-point AND/OR
- •(3)transient ST-elevation >1mm in 2 or more contiguous leads lasting
- •<30 min OR
- •(4)STE-ACS with onset <24 hours previously and chest pain > 30 min
- •ST-elevation > 1mm in 2 or more contiguous leads or new left bundle block
- •C) acute cerebrovascular disorders (trigger event), defined by:
- •i) a transient ischemic attack (TIA) with clinical restitution within 24h AND
- •initial neurological deficit verified by a neurologist OR ABCD2-Score >= 3 OR
- •visibleDWI-lesion (MRI) OR the main hospital diagnosis of Amaurosis fugax
- •ii) Ischemic stroke including retinal central artery occlusion
- •iii) stroke caused by non-traumatic intracerebral hemorrhage
- •iv) stroke caused by cerebral venous thrombosis
- •D) acute kidney injury while hospitalized, that occurred 3-8 days before study inclusion
- •(trigger event), defined by:
- •i) >= 2fold increase in creatinine compared to a respective value during a presumed
- •or documented time period (stage 2 or 3 acute kidney injury according to KDIGO)
- •ii) persistence of the increased value for at least 72 hrs
- •E) diabetes mellitus type 2 (at day 60)
- •i) known diabetes mellitus type 2 characterized by
- •(1) pathological findings in oral glucose tolerance test, OR
- •(2) documented HbA1c >= 6.5%, OR
- •(3) Intake of any antidiabetic medication
- •ii) prediabetes with high cardiovascular risk, characterized by
- •(1)HbA1c >5.7% and <6.5% AND an ESC score >= 5
排除标准
- •1) lack of capacity to give informed consent
- •2) pregnancy or lactation
- •3) life expectancy < 6 months due to non-cardio-/cerebrovascular diseases or conditions
- •4) organ transplanted
- •5) Lack of health insurance
研究者
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