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Detection of brown adipose tissue via MRI and multispectral optoacustic tomography (MSOT): Correlation with thermogenic capacity after cold exposure

Detection of brown adipose tissue via MRI and multispectral optoacustic tomography (MSOT): Correlation with thermogenic capacity after cold exposure

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00016629
Enrollment
60
Registered
2019-05-15
Start date
2019-03-11
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy participants

Interventions

Group 1: MRI is conducted on neck, adomen and pelvis, while heart rate and breathing are monitored. Depending on respiratory rate, measurements take 45-60 min. The MSOT device combines real-time imag

Sponsors

Lehrstuhl für ErnährungsmedizinZIEL ErnährungsmedizinTU München
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Only participants of the FREECE study (DRKS00010489) will be recruited.

Exclusion criteria

Exclusion criteria: Pregnancy, high skin pigmentation, documented or suspected photo-allergy, erythropoietic protoporphyria, allergic contact dermatitis, or very sensitive skin open or infected wounds of observed regions strong claustrophobia implants or metal pieces in the body pacemaker aneurysm clips in the brain cochlear implants, tympanostomy tubes

Design outcomes

Primary

MeasureTime frame
Aim of this thesis is to correlate resting metabolic rate (assesed in DRKS00010489) with volume of brown adipose tissue. Measuring the proton density fat fraction via MRI (PDFF-MRI) of neck and pelvis will shed light on this. Furthermore, a multispectral optoacustic tomography (MSOT) will be facilitated and its results compared with forementioned results in order to investigate the sensitivity of MSOT for the quantification of brown adipose tissue at basal conditions. MSOT will be applied in the supraclavicular fossae and a gluteal region for reference.

Secondary

MeasureTime frame
Secondary outcome is the association of these results with the data received by the FREECE study

Countries

Germany

Contacts

Public ContactClaudine Seeliger

Else Kröner-Fresenius-Zentrum für Ernährungsmedizin der TU München

claudine.seeliger@tum.de08161712006

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026