Hyperpolarized Xenon-129 Magnetic Resonance Imaging and Spectroscopy of Brown Fat: Healthy Adult Volunteer Pilot Study

Description

The primary goal of this study is to evaluate the feasibility of detecting Brown Adipose Tissue (BAT) in healthy subjects by using hyperpolarized xenon gas MRI. In this pilot study, MRI of BAT of healthy adult volunteers will be performed at 3 Tesla to assess image quality using a prototype surface coil and pulse sequence following inhalation of hyperpolarized 129Xe (xenon) gas at thermoneutrality and under mild cold condition. The investigators are testing the abilities of xenon MRI to see brown adipose tissue and detect its thermogenic activity.

Conditions

Obesity

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Study Overview

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Study Details

Study overview

The primary goal of this study is to evaluate the feasibility of detecting Brown Adipose Tissue (BAT) in healthy subjects by using hyperpolarized xenon gas MRI. In this pilot study, MRI of BAT of healthy adult volunteers will be performed at 3 Tesla to assess image quality using a prototype surface coil and pulse sequence following inhalation of hyperpolarized 129Xe (xenon) gas at thermoneutrality and under mild cold condition. The investigators are testing the abilities of xenon MRI to see brown adipose tissue and detect its thermogenic activity.

Phase 1 Study: Detection of Brown Adipose Tissue in Normal Volunteers Using a 3 Tesla (3T) Magnetic Resonance Imaging System and Hyperpolarized (HP) Xenon Gas

Hyperpolarized Xenon-129 Magnetic Resonance Imaging and Spectroscopy of Brown Fat: Healthy Adult Volunteer Pilot Study

Condition
Obesity
Intervention / Treatment

-

Contacts and Locations

Chapel Hill

Biomedical Research Imaging Center, Chapel Hill, North Carolina, United States, 27599-7513

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Ability to give informed consent
  • * Willing to participate in this study
  • * Male or female ≥ 18 years of age at the time of the interview.
  • * Subject has no diagnosed pulmonary condition
  • * Subject has not smoked in the previous 5 years
  • * Smoking history, if any, is less than or equal to 5 pack-years
  • * Written informed consent (and assent when applicable) obtained from subject or subject's
  • * legal representative and ability for subject to comply with the requirements of the study
  • * Healthy subject that may or may not have undergone an fluorodeoxyglucose -PET scan
  • * Any contraindication to MRI (presence of any non-removable metal implant, stents, pacemaker, clips, staples, or piercings, etc. )
  • * Subject does not fit in the magnet
  • * Pregnancy or breast feeding
  • * Severe claustrophobia
  • * Subject is less than 18 years old
  • * MRI is contraindicated based on responses to MRI screening questionnaire
  • * Subject is pregnant or lactating
  • * Respiratory illness of a bacterial or viral etiology within 15 days of MRI
  • * Subject has received an investigational medicinal product (not including 129Xe) within 30 days of MRI
  • * Subject has any form of known cardiovascular disease
  • * Subject cannot hold their breath for 15 seconds
  • * Subject deemed unlikely to be able to comply with instructions during imaging
  • * Subject is taking beta blockers
  • * Subject underwent an fluorodeoxyglucose-PET examination less than one week before the HP xenon MRI scan

Ages Eligible for Study

18 Years to 60 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

University of North Carolina, Chapel Hill,

Rosa Tamara Branca, PhD, PRINCIPAL_INVESTIGATOR, University of North Carolina, Chapel Hill

Study Record Dates

2028-01-01