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临床试验/NCT03278977
NCT03278977终止不适用

Apparent Life Threatening Events, Sudden Infant Death Syndrome and Muscarinic Receptors

University Hospital, Strasbourg, France8 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2018年9月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
发起方
入组人数
12
试验地点
8
主要终点
Muscarinic M2 receptor mRNA expression in blood

研究概览

简要总结

Apparent Life-Threatening Events (ALTE) in infants often lead to severe neurological complications or to sudden death. In such situations, cardio-pediatricians and intensive care physicians have no specific diagnosis or treatment. In a recent translational research (INSERM-DHOS), our team has reported a myocardiac abnormality in a rabbit model of vagal hyperreactivity which is also present in the human hearts of infants deceased from sudden death, i.e. increased M2 muscarinic receptors (M2R) density associated with compensative increased enzymatic activity and overexpression of acetylcholine esterase (AchE). In a recent PHRC-I study (article in preparation), these abnormalities have also been observed in the blood of patients, infants as well as adults, exhibiting severe vagal syncopes. We observed, even more importantly, similar abnormalities in infants under 1 year of age with very severe idiopathic ALTE (iALTE) compared with normal subjects and with patients who presented ALTE with identified etiologies (JAMA Pediatric, 2016 May). The aim of this present study is to validate the overexpression of M2R as a marker of risk of iALTE in infant under 1 year.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Single (Outcomes Assessor)

盲法说明

Blood sample analysis will be blinded

入排标准

年龄范围
28 Days 至 12 Months(Child)
性别
All
接受健康志愿者

入选标准

  • Infant aged between 28 days and 12 months, presenting severe syncope(s) requiring medical management, hospitalized in a pediatric intensive care unit or pediatric emergencies
  • Consent signed and dated by the legal representatives
  • Patients affiliated to a social security system

排除标准

  • Infant with known cardiovascular, neurologic, infectious, toxic or metabolic pathologies before enrollment (before the syncope)
  • Subject on medication for more than 3 months before enrollment
  • Impossibility to clearly inform the legal representatives (comprehension problems)
  • Subject in exclusion period for clinical trial (previous or current study)

研究组 & 干预措施

ALTE group

Other

Infants aged between 28 days and 12 months presenting severe(s) syncope(s) requiring hospitalization, for which a cause was identified during hospitalization.

干预措施: Blood sample for specific analyzes (Biological)

iALTE group

Other

Infant aged between 28 days and 12 months presenting a severe syncope(s) requiring hospitalization, for which no etiology was found during hospitalization.

干预措施: Blood sample for specific analyzes (Biological)

结局指标

主要结局

Muscarinic M2 receptor mRNA expression in blood

时间窗: At the admission in the hospital, within 24 hours after the inclusion in the study

Blood sample will be collected not later than 24 hours after the inclusion in the study and will be frozen until centralized analysis. A qRT-PCR will be performed for quantification of CHRM2 gene expression in blood (mRNA expression). Interim analysis with the 7-8 first samples per group together. Final analysis with all samples at the study completion.

次要结局

  • Acetylcholinesterase mRNA expression in blood(At the admission in the hospital, within 24 hours after the inclusion in the study.)

研究者

发起方
University Hospital, Strasbourg, France
申办方类型
Other
责任方
Sponsor

研究点 (8)

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