Register and DNA Bank of Adult Extra-hospital Sudden Death (Protocol FASTER)
2011年3月23日 更新者:Nantes University Hospital
Register and DNA Bank of Adult Extra-hospital Sudden Death
The main objective of this study is the formation of a DNA bank to realise a case-control genetic study designed to identify sequence variations in DNA that predispose to sudden cardiac death in adults.
The secondary objective of this study is the creation of a register for epidemiological surveillance of adult extra-hospital sudden death.
研究概览
研究类型
介入性
注册 (预期的)
2000
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
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Nantes、法国、44093
- Nantes university hospital
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 及以上 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
全部
描述
INCLUSION CRITERIA :
- Inclusion criteria for register :
- Adults ≥ 18 years of age.
- Persons who experienced sudden death defined as follows :cardiovascular arrest of non traumatic origin that occurred unexpectedly within an hour after the start of any prodromes.
- Patients not hospitalized at the time of sudden death.
- Inclusion criteria for DNA bank :
- Case subjects :
- Adults ≥ 18 years of age.
- Persons who experienced sudden death defined as follows :cardiovascular arrest of non traumatic origin that occurred unexpectedly within an hour after the start of any prodromes.
- Patients not hospitalized at the time of sudden death.
- Patients supported clinically by an emergency ambulance service.
- Control subjects :
- Adults ≥ 18 years of age.
- Adults hospitalized in an cardiac intensive care unit.
EXCLUSION CRITERIA :
- Exclusion criteria for register :
- Violent death : criminal, suicidal or accidental.
- Exclusion criteria for DNA bank :
- Case subjects :
- Violent death : criminal, suicidal or accidental.
- Identified cause of death extra-cardiac : neurological cause, hypoxia, pulmonary embolism, aortic rupture or other identified extra-cardiac cause.
- In accordance with Articles L1221-5 L1221-L1221-8 and 8-1 of the Code of Public Health, the categories of persons are excluded from research due to the fact that it can be achieved with an efficiency comparable over another class of people :
- Adult subject to legal protection measure,
- Pregnant woman,
- Parturient,
- Breastfeeding mother,
- Person deprived of liberty,
- Person hospitalised without his consent,
- Person admitted to a medical or socially facility.
- Control subjects :
- History of sudden death,
- Documented history of ventricular fibrillation,
- History of sustained ventricular tachycardia (lasting longer than 30 seconds) documented.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
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其他:控制对象
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A blood sample of 10 ml (2 x 5 ml) on two EDTA tubes will be realised and clinical data will be indicated in the CRF and the computerized database.
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其他:Case subjects
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A blood sample of 10 ml (2 x 5 ml) on two EDTA tubes will be realised on a route of vascular development place in the context of medical practice.Clinical data will be indicated in the CRF and the computerized database.
In the event an eligible patient has not been included during his support by an emergency ambulance service but, after successful resuscitation, he has been hospitalised in a cardiology department, its inclusion may be realised during the hospitalization by a physician investigator of the study.
A blood sample of 10 ml of 2 EDTA tubes will be realised on a route of vascular development in the context of routine care.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
|---|---|
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Identification of variants in DNA
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The primary endpoint is the identification of variants (polymorphisms and / or mutations) in DNA significantly associated with risk of extra-hospital sudden death in adults.
Study populations are : (i) the entire population of case subjects included in the DNA bank (ii) two subpopulations at high risk of sudden death : patients with a history of myocardial infarction and patients with LVEF < 30 %.
The variable analyzed is the nucleotide sequence of DNA in populations of case and control subjects.
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次要结果测量
结果测量 |
措施说明 |
|---|---|
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Annual incidence of extra-hospital sudden death in adults
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The annual incidence of extra-hospital sudden death in adults.
The variable analyzed is the number of incident cases per year of extra-hospital sudden death in adults.
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Annual mortality related to extra-hospital sudden death in adults
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The annual mortality related to extra-hospital sudden death in adults.
The variable analyzed is the number of annual deaths due to sudden death in adults.
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Characterization of victims of extra-hospital sudden death in adults
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The characterization of victims of extra-hospital sudden death in adults, their medical care in emergency and their future from D0 to D28.
Variables analyzed are clinical data are collected in case report forms.
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:Vincent PROBST, Profesor、CHU de Nantes
- 学习椅:Jean-Luc CHASSEVENT, Doctor、University Hospital, Angers
- 学习椅:Nicolas HOURDIN, Doctor、CH de Châteaubriant
- 学习椅:Yves-Marie PLUCHON, Doctor、CH de La roche-sur-yon
- 学习椅:Christophe SAVIO, Doctor、CH du Mans
- 学习椅:Jean-Pierre AUFFRAY, Profesor、CHU de Marseille
- 学习椅:Christian HAMON, Doctor、CH de Saint-Brieuc
- 学习椅:Christophe BERRANGER, Profesor、CH de Saint-Nazaire
- 学习椅:Jean-Louis DUCASSE, Doctor、University Hospital, Toulouse
- 学习椅:BOULANGER, Doctor、CH DE VANNES
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2007年6月1日
初级完成 (实际的)
2010年11月1日
研究完成 (实际的)
2010年11月1日
研究注册日期
首次提交
2011年3月23日
首先提交符合 QC 标准的
2011年3月23日
首次发布 (估计)
2011年3月24日
研究记录更新
最后更新发布 (估计)
2011年3月24日
上次提交的符合 QC 标准的更新
2011年3月23日
最后验证
2011年3月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.