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Clinical Trial

Evaluation of Gadolinium Based Contrast Agents for Portable MR Imaging Systems

NCT: NCT07296263 · ENROLLING_BY_INVITATION

NCT IDNCT07296263
StatusENROLLING_BY_INVITATION
Start Date2025-12-30
Completion2026-10-31

Brief Summary

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.

Frequently Asked Questions

What is Evaluation of Gadolinium Based Contrast Agents for Portable MR Imaging Systems?

Evaluation of Gadolinium Based Contrast Agents for Portable MR Imaging Systems is a clinical trial registered under NCT07296263. Current status: ENROLLING_BY_INVITATION.

What is the status of NCT07296263?

The current status of NCT07296263 (Evaluation of Gadolinium Based Contrast Agents for Portable MR Imaging Systems) is: ENROLLING_BY_INVITATION.

When did Evaluation of Gadolinium Based Contrast Agents for Portable MR Imaging Systems start?

Evaluation of Gadolinium Based Contrast Agents for Portable MR Imaging Systems started on 2025-12-30.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.