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临床试验

Evaluation of Gadolinium Based Contrast Agents for Portable MR Imaging Systems

NCT:NCT07296263 · ACTIVE_NOT_RECRUITING

NCT编号NCT07296263
状态ACTIVE_NOT_RECRUITING
开始日期2025-12-30
完成时间2026-10-31
SponsorHyperfine (INDUSTRY)
First posted
Last updated

简要摘要

This is a prospective, multi-center, interventional study designed to evaluate the visualization benefits of FDA approved gadolinium-based contrast agents (GBCAs) in portable magnetic resonance imaging (pMRI) of the brain. The study will enroll adult patients with known or suspected brain lesions involving blood-brain barrier disruption. Each participant will undergo a pre-contrast pMRI scan, receive an intravenous GBCA injection, and then complete a post-contrast pMRI scan using the Swoop® Portable MR Imaging® System. Lesion visualization will be assessed by independent neuroradiologists using standardized scoring criteria. The study will be conducted across a minimum of three sites to ensure diversity in patient population, imaging environments, and GBCA types.

官方来源

在 ClinicalTrials.gov 上查看 →

数据来自 ClinicalTrials.gov API。有关最新状态,请参阅官方记录。

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