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临床试验/NCT05090956
NCT05090956已完成不适用

Mise au Point de Protocoles RMN Sur l'Imageur Philips 3T installé Sur le Site du Pavillon Baudot du CHU Purpan à Toulouse

Institut National de la Santé Et de la Recherche Médicale, France1 个研究点 分布在 1 个国家目标入组 230 人开始时间: 2012年6月8日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
230
试验地点
1
主要终点
quality of MRI images

研究概览

简要总结

Since January 2010, a new magnetic resonance imaging scanner (Philips 3T, Achieva) is installed on the Baudot Building in Toulouse hospital. This tool, is completely dedicated to the research. It was installed with sequences RMN supplied by the manufacturer.

Imagers also contain an instrumentation susceptible to evolution and/or to adjustment (antennas radio frequency, sheath of gradients, elements of physiological monitoring (for example control of the breath), regulation of the homogeneity of the magnetic field).

This MRI scanner and this instrumentation are used for anatomical examinations or for paradigms of cognitiveresearch (for example of detection of intellectual activations following simple stimuli of fingers movement, visual tasks, or of mental processes).

The developpement of this equipment is going to favor the emergence of numerous projects and new themes, up to there adressed by other techniques (psychophysics, EEG).

To obtain good quality signals and know the practical limits of this imager, it is thus necessary that the researchers doctors, physicists and engineers, can finalize on volunteers' significant number, all the sequences RMN necessary for the use of these tools for the research.

These developments are going to get organized around four main axes:

1 the control of the geometrical distortions (generated by the introduction of an object within the magnetic field) 2 Optimization of the parameters of sequences to improve the contrast and the spatial resolution of the obtained images 3 the development of new sequences 4 the feasibility study of the protocols of functional MRI

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

入选标准

  • Healthy adult, age = 18 years;
  • Visual, hearing , oral or written capacities and expression sufficient for the suitable realization of the tests;
  • Obtaining of the informed consent of the subject.

排除标准

  • Subjects presenting a neurological, psychiatric history;
  • Subjects under chronic medication which can influence the intellectual activity;
  • Subjects presenting a contraindication to the MRI (carriers of a pacemaker, an implanted material(equipment) activated by an electric, magnetic or mechanical system, carriers of haemostatic clips of anévrysmes intracérébraux or carotid arteries, carriers of orthopaedic, claustrophobic implants);
  • Subjects refusing to be informed about the possible presence of an anatomical anormality;
  • administrative Problems: impossibility to give about the information, no insurance, refusal to sign the consent, under guardianship subject ;
  • Subjects participating in another protocol • pregnancy

研究组 & 干预措施

control

Experimental

MRI exam; The sequences to be performed will be presented to the subject according to the focus to be performed. maximal duration of the exam: 2 hours (including subject set up)

干预措施: mri (Other)

结局指标

主要结局

quality of MRI images

时间窗: 90 months

assessment of distortion of MRI images

Assessment of distortion of MRI images

时间窗: 90 months

Measurement of contrasts of MRI sequence

时间窗: 90 months

By using available software such as MRICro, Image J, Matlab or other post-processing tools developed as required

Measurement of MRI sequence resolution

时间窗: 90 months

To estimate the resolution by measuring the signal-to-noise ratio using standard software such as MRICro, Image J, Matlab or other post-processing tools developed as required

次要结局

未报告次要终点

研究者

发起方
Institut National de la Santé Et de la Recherche Médicale, France
申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

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