Protocol development for a Hyperfine Very Low Field (0.064 T) MRI system

Recruiting

• Conditions: MR protocol development; N.A.

• Registration Number: NL-OMON51553
• Lead Sponsor: Radiologie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 9 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 120

Inclusion Criteria

Healthy volunteers between the age >18 years or <65 years

Exclusion Criteria

- Age <18 years or >65 years
- Persons with reduced mental capacity
- Pregnancy and a chance of being pregnant (as reported by the volunteer)
- Not having a general practitioner
- MRI contraindication e.g. cardiac pacemaker, implants not approved for MRI
(see www.mrisafety.com), claustrophobia, tinnitus, metal objects attached to
the body that cannot be removed

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The main study parameters of this project are quantitative measurements of MR<br /><br>parameters. Specifically, we will measure T1, T2, T1*, T2*, magnetisation<br /><br>transfer and diffusion in the human brain. From this data, we will perform<br /><br>quantitative analysis (signal-to-noise ratio (SNR), contrast-to-noise ratio<br /><br>(CNR)). Having measured these, we will design optimized imaging protocols which<br /><br>will be quantitatively compared with those currently available on the system</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>None</p><br>