Multi-Parametric MRI Assessment of the Liver in the Dallas-FortWorth Metroplex Population

Completed

• Conditions: Non-Alcoholic Fatty Liver Disease

• Registration Number: NCT04336618
• Lead Sponsor: Perspectum

Brief Summary

To build a Registry of volunteers by inviting them to get a LiverMultiScan(LMS)and collecting their contact information to seek interest in participating in future studies.

Detailed Description

This is a Registry where there will be no intervention to the standard of care.Participants will be required to attend a single visit that will involve having a multi-parametric MRI at no cost to them. In addition, the invesigators will collect contact information of participants including their email address, phone number and house address so that they can be contacted to discuss possible participation in future studies which may be sponsored by Perspectum or third parties, such as pharmaceutical companies, the participants personal information shall never be shared with these third-parties. Additionally, the contact information of the participants medical providers shall be collected so that, if requested, their LMS reports can be used in their diagnostic pathway.

Imaging will be performed at two Touchstone Imaging locations, one in downtown Dallas and the other in Southlake.

A total of 100 participants will be enrolled over a period of 1 year.

Study Timeline

• Study First Submitted: 2020-04-03
• Study First Submitted QC: 2020-04-06
• Study First Posted: 2020-04-07
• Study Start: 2020-08-03
• Primary Completion: 2022-09-27
• Study Completion: 2022-09-27
• Status Verified: 2023-12
• Last Update Submitted: 2023-12-21
• Last Update Posted: 2023-12-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 67

Inclusion Criteria

• Male or female volunteers aged 18 years and over•
• Participant willing and able to give informed consent for participation in the registry.

Exclusion Criteria

• The participant may not enter the Registry if they have any contraindication to magnetic resonance imaging (standard MR exclusion criteria at the imaging center including pregnancy, extensive tattoos, pacemaker, shrapnel injury, severe claustrophobia).

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To build a Registry of volunteers by inviting them to get a LiverMultiScan(LMS)and collecting their contact information to seek their interest in participating in future studies	12 months

Secondary Outcome Measures

Name	Time	Method
To use multi-parametric MRI (LMS) of the liver to assess the volunteer's liver health	12 months

Trial Locations

Locations (1)

Perspectum Inc.; 🇺🇸 Dallas, Texas, United States