The Spiral MRI Study

NCT07167953 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 131

Last updated 2025-09-17

No results posted yet for this study

Summary

The goal of this clinical trial is to find out if new Magnetic Resonance Imaging (MRI) computer software will:

* help make scans and exams faster
* reduce artifacts
* make MRI easier to understand
* allow technicians to focus more on the participant and less on the scanner

Participants will complete one brain MRI imaging session, lasting about 60 minutes.

Conditions

  • Brain MRI

Interventions

DEVICE

Brain MRI

90 participants will undergo a 60 minute SOC brain MRI followed by 15 minute spiral MRI

DEVICE

Brain MRI - SOC and spiral

6 participants will be scanned using 2 versions (SOC and spiral) pf 6 sequences (12 scans total).

DEVICE

Brain MRI - spiral

10 participants will be scanned with 3 sequences, 3 times (9 total scans per participants)

DEVICE

Brain MRI - SOC and spiral

10 participants will be scanned using 2 versions (SOC and spiral) of 6 sequences (12 scans total).

DEVICE

Brain MRI - spiral

10 participants will be scanned with 3 spiral sequences to achieve desired signal to noise ratio (SNR).

DEVICE

Brain MRI - spiral

5 participants will be scanned with 2 pairs of 6 spiral sequences.

Sponsors & Collaborators

  • National Institute for Biomedical Imaging and Bioengineering (NIBIB)

    collaborator NIH
  • University of Wisconsin, Madison

    lead OTHER

Principal Investigators

  • James Pipe, PhD · University of Wisconsin, Madison

Study Design

Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2028-08-31
Primary Completion
2031-05-31
Completion
2031-05-31
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07167953 on ClinicalTrials.gov