跳至主要内容
临床试验/NCT04717843
NCT04717843招募中不适用

Identification of New Markers of Atrial Myopathy in Patients With Embolic Stroke of Undetermined Source (ESUS) From MRI 4D Data

Hospices Civils de Lyon3 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2021年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
40
试验地点
3
主要终点
Mean flow velocities in the left atrium

研究概览

简要总结

Atrial myopathy is considered to be the underlying cause of a large proportion of embolic strokes of undetermined source. However, the definition of this atrial condition is not well delineated while its identification could lead to prescription on anticoagulation in order to avoid stroke recurences. This study aims to identify new markers of atrial myopathy and choosed a multi parametric approach with electrical, echographical, biological and 4D flow CMR derived markers.

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
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Groupe1:Ischemic embolic stroke of undetermined source (ESUS) according to TOAST criteria (N =10)
  • •Age ≥ 18 years old
  • •Non-gap ischemic stroke diagnosed on MRI or CT scan of the brain (gap stroke defined as a cerebral infarction ≤ 1.5 cm / ≤2.0 cm on diffusion sequences).
  • •No major cardio-embolic source (episode of atrial fibrillation or flutter > 6min, intracardiac thrombus, LVEF <30 percent recent myocardial infarction (<4 weeks), mitral stenosis, valvular vegetation or infectious endocarditis).
  • •Absence of atherosclerosis causing stenosis ≥ 50 percent of the lumen of the intra or extra cranial arteries that vascularise the infarcted cerebral area.
  • •No other specific cause identified (arteritis, arterial dissection, migraine/vaso-spasm, toxic cause).
  • •Affiliation to a social security scheme
  • •Patient who signed the consent
  • •Group 2: Non-paroxysmal AF (N=10)
  • •Age ≥ 18 years old
  • •Subject with documented non-paroxysmal AF
  • •Affiliation to a social security scheme
  • •Patient who signed the consent
  • •Group 3: Healthy volunteers (N=10)
  • •Pre-inclusion criteria :
  • •Age ≥ 45 years old
  • •Patient with no documented cardiac or neuro-vascular history
  • •Affiliation to a social security scheme
  • •Patient who signed the consent
  • •Registration on the VRB file (Volontaires Recherches Biomédicales, https://vrb.sante.gouv.fr) or response to the published announcement
  • •Criteria for inclusion :
  • •ECG in sinus rhythm
  • •Holter ECG: no AF
  • •Normal Trans thoracic echocardiography
  • •Patient with no neuro-vascular history
  • •Group 4: Stroke-ESUS or non-paroxysmal AF with cardiac MRI (N=10)
  • •Age ≥ 18 years old
  • •Subject with a documented stroke-ESUS or documented non-paroxysmal FA
  • •Subject with cardiac MRI
  • •Affiliation to a social security scheme
  • •Subject having given its non-opposition

排除标准

  • •Groupe1: Ischemic embolic stroke of undetermined source (ESUS) according to TOAST criteria (N =10)
  • •Risk of pregnancy or pregnancy (proven on interrogation data or pregnancy test).
  • •Contraindication to MRI ferromagnetic material (in particular pacemaker, implantable defibrillator, cardiac valve prosthesis, cochlear implant, neuro-stimulator, implanted automated injection material, intraocular metallic foreign body, neurosurgical and vascular clips, claustrophobia)
  • •Less than 8 weeks after implantation of a stent
  • •Subject participating in another intervention research including a period of exclusion still in progress at the pre-inclusion stage.
  • •Group 2: Non-paroxysmal AF (N=10)
  • •Risk of pregnancy or pregnancy (proven on interview data or pregnancy test).
  • •Contraindication to MRI ferromagnetic material (in particular pacemaker, implantable defibrillators, cardiac valve prosthesis, cochlear implant, neurostimulators, implanted automated injection equipment, intraocular metallic foreign body, neurosurgical and vascular clips, claustrophobia).
  • •Less than 8 weeks after implantation of a stent
  • •Subject participating in another intervention research including a period of exclusion still in progress at the pre-inclusion stage.
  • •Group 4: Stroke-ESUS or non paroxysmal AF with cardiac MRI (N=10)
  • •History of neuro-vascular or cardiac pathology
  • •Risk of pregnancy or pregnancy (proven on interrogation data or pregnancy test).
  • •Contraindication to MRI (ferromagnetic material (in particular pacemaker, implantable defibrillator, cardiac valve prosthesis, cochlear implant, neuro-stimulator, implanted automated injection material, intraocular metallic foreign body, neurosurgical and vascular clips, claustrophobia)
  • •Subject participating in another intervention research including a period of exclusion still in progress at the pre-inclusion stage.

研究组 & 干预措施

Patients with embolic strokes of undetermined source.

Experimental

Patients over 18 years old, with embolic strokes of undetermined source, fulfilling the TOAST criteria. The intervention consists of a 4D Flow MRI.

干预措施: 4D Flow MRI (Other)

Patients with non-paroxysmal AF.

Experimental

Patients over 18 years old, with non-paroxysmal AF. The intervention consists of a 4D Flow MRI.

干预措施: 4D Flow MRI (Other)

Heathy volunteers

Active Comparator

The control group will include volunteers over 45 years old with no history of cardio-vascular or neuro-vascular disease. The last will be certified by a pre inclusion protocol containing a medical consultation, a Holter ECG and a trans-thoracic echocardiography. The age of 45 was chosen to get comparable age group and set the analyses free of the age-related effect on the cardiac hemodynamic. The intervention consists of an ECG, holter ECG, Trans thoracic echocardiography ETT, Blood sample and 4D Flow MRI.

干预措施: 4D Flow MRI (Other)

Heathy volunteers

Active Comparator

The control group will include volunteers over 45 years old with no history of cardio-vascular or neuro-vascular disease. The last will be certified by a pre inclusion protocol containing a medical consultation, a Holter ECG and a trans-thoracic echocardiography. The age of 45 was chosen to get comparable age group and set the analyses free of the age-related effect on the cardiac hemodynamic. The intervention consists of an ECG, holter ECG, Trans thoracic echocardiography ETT, Blood sample and 4D Flow MRI.

干预措施: Medical consultation with 12 leads ECG (Other)

Heathy volunteers

Active Comparator

The control group will include volunteers over 45 years old with no history of cardio-vascular or neuro-vascular disease. The last will be certified by a pre inclusion protocol containing a medical consultation, a Holter ECG and a trans-thoracic echocardiography. The age of 45 was chosen to get comparable age group and set the analyses free of the age-related effect on the cardiac hemodynamic. The intervention consists of an ECG, holter ECG, Trans thoracic echocardiography ETT, Blood sample and 4D Flow MRI.

干预措施: Holter ECG (Other)

Heathy volunteers

Active Comparator

The control group will include volunteers over 45 years old with no history of cardio-vascular or neuro-vascular disease. The last will be certified by a pre inclusion protocol containing a medical consultation, a Holter ECG and a trans-thoracic echocardiography. The age of 45 was chosen to get comparable age group and set the analyses free of the age-related effect on the cardiac hemodynamic. The intervention consists of an ECG, holter ECG, Trans thoracic echocardiography ETT, Blood sample and 4D Flow MRI.

干预措施: Trans thoracic echocardiography (Other)

Heathy volunteers

Active Comparator

The control group will include volunteers over 45 years old with no history of cardio-vascular or neuro-vascular disease. The last will be certified by a pre inclusion protocol containing a medical consultation, a Holter ECG and a trans-thoracic echocardiography. The age of 45 was chosen to get comparable age group and set the analyses free of the age-related effect on the cardiac hemodynamic. The intervention consists of an ECG, holter ECG, Trans thoracic echocardiography ETT, Blood sample and 4D Flow MRI.

干预措施: Blood sample (Biological)

ESUS and non-paroxysmal AF patients with cardiac MRI

Experimental

ESUS and non-paroxysmal AF patients (fulfilling the group 1 et 2 criteria) and who had had cardiac MRI, in a retrospective way. It corresponds to retrospective inclusion of patients which had MRI in the year before the beginning of the study.

干预措施: Standard MRI (Other)

结局指标

主要结局

Mean flow velocities in the left atrium

时间窗: One Day

Velocity magnitude (cm/s) for all atrial voxels and all cardiac frames will be plotted in a histogram and normalized by the total number of voxels to allow comparisons between subjects

次要结局

  • Vortex size(One Day)
  • Left atrium volume(One Day)
  • Left atrium stasis(One Day)
  • Maximal flow velocities in the left atrium(One Day)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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