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临床试验/NCT04341701
NCT04341701进行中(未招募)不适用

Phenotype Identification Based on Multimodal MRI Analysis of Patients With Bronchial Obstructive Diseases

University Hospital, Bordeaux12 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2021年8月5日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
100
试验地点
12
主要终点
Determine the number of the clusters

研究概览

简要总结

The hypothesis is that pulmonary and cardiac proton MRI allows phenotyping of patients with bronchial obstruction by cluster analysis based on quantitative multimodal imaging of bronchi, pulmonary vessels, pulmonary parenchyma, right and left ventricular function, myocardial fibrosis and pulmonary arterial pressure.

Such imaging will also offer the advantage of being non-irradiating and without contrast products, which will ultimately allow CT to be replaced by MRI in the follow-up of bronchial obstructive patients, thus avoiding the risks associated with repeated exposure to ionizing radiation.

详细描述

Bronchial obstructive diseases such as asthma and chronic obstructive pulmonary disease (COPD) are very common and represent a major public health problem. The distinction between these two diseases is sometimes difficult. In each of these diseases, several clinical phenotypes or biological endotypes have been defined. For example, frequent exacerbating patients and / or hypereosinophilic patients are present in both diseases. In the severe states, cardiovascular comorbidities are the most frequent comorbidities and alter the prognosis.

In these chronic obstructive patients, computed tomography (CT) allows a multimodal analysis of the bronchial wall, the lung parenchyma and pulmonary vessels. CT also allows a score analysis of coronary plaques. However, irradiation is significant and increases with repeated examinations. CT does not allow a comprehensive analysis of cardiac function, or an estimate of pulmonary artery pressure.

Magnetic Resonance Imaging (MRI) is a proton non-ionizing alternative to CT, in particular when using 3D ultra-short echo-time (UTE) sequences. These 3D-UTE sequences decrease the effects of magnetic susceptibility and provide morphological and morphometric information on bronchi and lung comparable to those obtained by CT. Moreover, dedicated sequences add functional information on bronchi. Heart MRI allows more analyses, such as right and left ventricular systolic functions, an indirect estimate of pulmonary arterial pressure and the amount of diffuse myocardial fibrosis.

Our project aims to identify morphological phenotypes through the pulmonary and heart MRI in patients with obstructive lung disease

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研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
40 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Man or woman aged between 40 and 70 years.
  • Having benefited under the current care of spirometry showing FEV / FVC pre-bronchodilation <0.70 at steady state (i.e., without exacerbation from at least 4 weeks).
  • Having a diagnosis of asthma according to GINA 2019 without smoking restrictions or COPD according to GOLD 2019 but unrestricted to any level of bronchial reversibility to bronchodilator established by the pulmonologist.
  • On stable cardiopulmonary medications for at least 4 weeks
  • Having given his written informed consent.

排除标准

  • Subject deprived of liberty by judicial or administrative decision.
  • Major protected by law.
  • Subject not affiliated to a social security scheme, whether or not the beneficiary of such a regime.
  • Pregnant or breastfeeding women
  • Inability to complete the Questionnaire SF-36 and SGQLQ.
  • Subject in times of exclusion in relation to another protocol.
  • History of pulmonary fibrosis, primary pulmonary hypertension and cystic fibrosis.
  • History of lung resection (referred to oncological or volume reduction)
  • History of cancer except skin cancer (squamous and Basal) under 5 years
  • History of chest radiation
  • Pacemaker carrier subject or implantable defibrillator, intraocular metallic foreign body, metal clip intracranial, heart valve prosthesis kind Starr-Edwards pre-6000, or biomedical insulin pump type device, Neurostimulator or cochlear implant, Metal patches.
  • Subject claustrophobic or unable to stay elongate during 30 minutes.
  • Subject with a waist circumference greater than 200 cm.
  • Occurrence of an exacerbation between the FE and MRI
  • Uninterpretable MRI

结局指标

主要结局

Determine the number of the clusters

时间窗: Day 30

Number of the clusters will be defined using principal component analysis and dendrogram, based on the multimodal lung and heart MRI analysis

Determine the Quality of the clusters

时间窗: Day 30

Quality of the clusters will be defined using Dunn index and non-hierarchical analysis based on the multimodal lung and heart MRI analysis

次要结局

  • Determine of slow Vital Capacity (VC) during spirometry before and after bronchodilator(day 1)
  • Determine of Forced Expiratory Volume in one sec (FEV-1) during spirometry before and after bronchodilator(day 1)
  • Determine the value of blood total IgE at(day 1)
  • Assessment of tobacco consumption(Day 1)
  • Assessment of disease duration(Day 1)
  • Evaluation score of SF-36 questionnaire(Day 1)
  • Determine of Forced Vital Capacity (FVC) during spirometry before and after bronchodilator(day 1)
  • Determine of Functional Residual Capacity (FRC) during spirometry before and after bronchodilator(day 1)
  • Determine the value of blood B-type natriuretic peptide(day 1)
  • Determine the value of blood total IgE(day 1)
  • Evaluation with St Georges Quality of Life Questionnaire(Day 30)
  • Evaluation of comorbidities(Day 1)
  • Determine of Total Lung Capacity (TLC) during spirometry before and after bronchodilator(day 1)
  • Determine of Residual Volume (RV) during spirometry before and after bronchodilator(day 1)
  • Assessment of age(Day 1)
  • Assessment of sexe(Day 1)
  • Determine the value of blood eosinophils(day 1)
  • Determine the value of blood C-reactive protein(day 1)
  • Determine of Carbon monoxide transfer capacity (TLCO)(day 1)
  • Determine the value of blood heamoglobin(day 1)

研究者

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

研究点 (12)

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