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Recruiting NCT07444034

A Pilot Study of a Portable Head-Only MRI Scanner

No phase Interventional Brain Imaging

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: 0.7 T MRI.
Who it may be relevant to
Registry conditions: Brain Imaging. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This is a pilot study to demonstrate human brain imaging with a new portable 0.7 Tesla (T) MRI brain scanner recently developed at the CMRR.

Interventions

  • Device 0.7 T MRI
    Our scanner is based on a unique high-temperature superconducting magnet that is highly compact, weighs only 400 kg, and requires no cryogens. Its innovative design allows the subject to sit normally with sightlines to the room and produces low acoustic noise during scanning.

Primary outcome measures

  • Image Quality [Time frame: Day 1]

Eligibility criteria

Inclusion criteria

  • 18 years of age or older
  • Able to consent for themselves
  • Free of contraindications for MRI

Exclusion criteria

  • Currently pregnant
  • Extremely claustrophobic

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Basic science

Study locations

United States · 1 center
  • University of Minnesota — Minneapolis

Identifiers

NCT: NCT07444034 · CMRR-2025-33869

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗