University Hospital Basel, Department of Endocrinology
Basel, 4031, Switzerland
Location status: Recruiting
NCT Number: NCT06978777
The purpose of the study is to asses brown adipose tissue activity after a cold mild stimulus, preceded by 200mg caffeine or placebo administration.
Interested in participating?
Request Info18 year–40 year
All sexes
Interventional
Not applicable
Basel, 4031, Switzerland
Location status: Recruiting
Brown adipose tissue (BAT) activation is typically through beta3-adrenoceptors (beta3-AR), but beta3-alone are less efficacious than cold in activating human BAT. Recent research suggests that adenosine, released during cold exposure, plays a key role in BAT thermogenesis. This study aims to investigate the role of the adenosine A2A receptor (A2AR) in BAT activation through a randomized trial with mild cold exposure and caffeine, a potent A2AR antagonist, to explore new therapeutic strategies for metabolic diseases.
This is a randomized, double-blind, placebo-controlled cross-over trial involving healthy volunteers. The study includes a screening visit and two main study visits (A and B), which will occur in random order.
During the two study visits, resting energy expenditure will be assessed by indirect calorimetry under warm conditions and following mild cold exposure, after administration of either caffeine or placebo. For cold exposure, participants will wear cooling sleeves around the waist, which gradually lower the surface body temperature to 10°C or to the lowest tolerable temperature without inducing shivering.
Additionally, BAT activity will be assessed using 18F-FDG PET/CT, performed 30 minutes after the 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
single dose of 200mg caffeine orally in study visit A
single dose of 1 tablet Placebo in study visit B
Time frame: 30 minutes after end of intervention in study visit A and B.
Description: 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 in study visit A and B.
maximum SUV in supraclavicular adipose tissue (according to BARCIST 1.0) as determined by 18F-FDG PET-CT after the respective study intervention
Time frame: 30 minutes after intervention in study visit A and B.
volume of supraclavicular adipose tissue (according to BARCIST 1.0) as determined by 18F-FDG PET-CT after the respective study intervention.
Time frame: immediately after the intervention (caffeine or placebo)
rise in energy expenditure above baseline occurring during mild cold exposure in the respective study intervention.
Time frame: immediately after the intervention (caffeine or placebo)
REE during warm conditions and at the end of cold exposure.
Time frame: immediately after the intervention (caffeine or placebo)
Ratio between carbon dioxide production and oxygen consumption (VCO2/VO2) during the enregy expenditure (EE) measurements.
Time frame: immediately after the intervention (caffeine or placebo)
Changes in skin temperature after mild cold stimulus. It will be measured during the hole study visits during warm condition and after cold stimulation, using wireless temperature sensors (iButton Thermochron) attached to the skin at 11 pre-defined locations
Time frame: immediately after the intervention (caffeine or placebo)
Plasma metabolome and lipidome profiles.
Time frame: immediately after the intervention (caffeine or placebo)
Plasma caffeine and its metabolites.
Contact information is provided by the study sponsor or research team.
Jaël Senn, MD
CONTACT
Matthias Betz, Prof.
CONTACT
University Hospital, Basel, Switzerland
Other
Acronym: ACROBAT
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.
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