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临床试验/NCT05744102
NCT05744102尚未招募不适用

Evaluation of Advanced and New MRI Techniques to Improve Patient Diagnosis

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 2,016 人开始时间: 2023年3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
尚未招募
入组人数
2,016
试验地点
1
主要终点
Image quality

研究概览

简要总结

The main objective of the research is to compare by two blind evaluators new MRI techniques with routinely used sequences.

详细描述

"The main evaluation criterion will be the choice of the two (or three) evaluators as to the best sequence between the new sequence and the standard sequence.

The decision criterion for considering a new sequence as superior to the standard sequence will be based on two measures:

  1. The proportion of patients for whom the new sequence was preferred, which must be greater than or equal to 75%;
  2. Inter-observer agreement (Cohen's Kappa coefficient), which must be greater than or equal to 0.8; When these two criteria are met, the new sequence will be considered superior to the standard sequence"

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Adult patient
  • •Patient who signed a consent to participate in the study
  • •Affiliated patient or beneficiary of a social security scheme
  • •Patient having an MRI scheduled as part of their care pathway
  • •Absence of prohibition of participation in another research

排除标准

  • •Patients under guardianship or curators
  • •Pregnant or breastfeeding patients
  • •Patients responding to a contraindication to performing an MRI
  • •Patient under state medical aid (AME)
  • •Adult patients protected by law

研究组 & 干预措施

Adult patients having MRI planned at Paul Brousse Hospital

Other

Evaluate new MRI sequences on a population of patients undergoing MRI as part of their usual care

干预措施: MRI Image (Diagnostic Test)

结局指标

主要结局

Image quality

时间窗: 7 years

The main evaluation criterion will be the choice of the two (or three) evaluators as to the best sequence between the new sequence and the standard sequence.

次要结局

  • Acquisition period(7 years)
  • Apnea(7 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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