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Recruiting

NCT Number: NCT02663362

Development and Validation of Multi-nuclear Magnetic Resonance Imaging and Spectroscopy for Whole Body Human Applications

The purpose of this study is to develop and refine the techniques for using magnetic resonance imaging and magnetic resonance spectroscopy to understand the composition and function of the human body

Recruiting

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Key information

Age range

12 year–89 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Translational Research Institute for Metabolism and Diabetes

Orlando, Florida, 32804, United States

Location status: Recruiting

Location contact

Heather Cornnell, PhD

PRINCIPAL_INVESTIGATOR

Recruitment Manager

CONTACT

[email protected]

407-303-7100

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female
  • Age 12 - 89
  • Healthy (self assessed)
  • Weight under 350lbs
  • Able to walk 50 yards without stopping
  • Able to travel to hospital for study visits
  • Able to follow a 3-step command
  • Able to remain in Magnetic Resonance (MR) scanner for up to 2 hours

Exclusion criteria

  • Have internal metal medical devices, including cardiac pacemakers, aortic or cerebral aneurysm clips, artificial heart valves, ferromagnetic implants, shrapnel, wire sutures, joint replacements, bone or joint pins/rods/screws, metal fragments in your eye, or non-removable jewelry such as rings.
  • Are unwilling or unable to complete the imaging procedures for the duration of the MRI scan due to claustrophobia or other reason.
  • Serious mental illness that might preclude subject's ability to comply with study treatment
  • Life expectancy of less than 1 year
  • Are pregnant or plan on becoming pregnant in the next 8 weeks.

Treatment and study plan

To evaluate the reproducibility of acquiring multi-nuclear data on a new 3T Philips Magnet

Other

Outside standard MR instrumentation there will be no interventions.

Primary outcomes

  1. Whole body fat quantification

    Time frame: 1 hour

Secondary outcomes

  1. Fat Microstructure

    Time frame: 1 hour

    A high resolution image of the structure of fat tissue.

Other outcomes

  1. Flow high resolution imaging

    Time frame: 1 hour

    Image of the movement of fluids in the area being imaged.

  2. Intramyocellular fat quantification

    Time frame: 45 minutes

    Use to determine the amount and types of fat inside muscle and liver.

  3. Intrahepatic fat quantification

    Time frame: 45 minutes

    A measure of the amount of fat in the liver.

Study contacts

Contact information is provided by the study sponsor or research team.

Recruitment Department

CONTACT

[email protected]

407-303-7100

Sponsors and collaborators

Lead sponsor

AdventHealth Translational Research Institute

Other

Registry information

Acronym: MRS VALIDATION

Important dates

Study start
2012
Primary completion
2026
Study completion
2027
First posted
Jan 26, 2016
Registry last updated
Mar 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.