University Hospital Basel, Dept. of Endocrinology
Basel, Switzerland
NCT Number: NCT05294965
The purpose of the study is to asses brown adipose tissue activity in humans after intravenous administration of the selective beta-2-adrenergic agonist fenoterol as compared to the natural activator of brown adipose tissue, a mild cold stimulus.
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Notify Me18 year–40 year
All sexes
Interventional
Early Phase 1
Basel, Switzerland
The activation of brown adipose tissue in response to beta-2-adrenergic stimulation as compared to cold exposure will be studied in an open-label, cross-over trial in healthy volunteers with random sequence of the two study interventions a) and b):
Energy expenditure will be measured during both interventions by indirect calorimetry and brown adipose tissue activity will determined by 18F-FDG-PET/CT 30 min after injection of 75 MBq of 18F-FDG.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Intravenous infusion
Other names: beta2 adrenoreceptor agonist
Body surface cooling
Time frame: 30 minutes after end of intervention
18F-FDG uptake into the supra-clavicular brown adipose tissue as determined by 18F-FDG PET-CT after the respective study intervention
Time frame: 30 minutes after intervention
maximum SUV in supraclavicular adipose tissue (according to BARCIST 1.0)
Time frame: 30 minutes after intervention
volume of supraclavicular adipose tissue (according to BARCIST 1.0)
Time frame: 30 minutes after intervention
volume of supraclavicular adipose tissue x SUVmean (according to BARCIST 1.0)
Time frame: First and last 30 minutes of intervention
Quantitative change in EE above resting metabolic rate in response to the respective study intervention. Measured by indirect calorimetry.
University Hospital, Basel, Switzerland
Other
Acronym: ASCENT
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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.
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