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NCT Number: NCT06978777

Effect of Caffeine on Cold-stimulated Brown Adipose Tissue Activity

The purpose of the study is to asses brown adipose tissue activity after a cold mild stimulus, preceded by 200mg caffeine or placebo administration.

Recruiting

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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital Basel, Department of Endocrinology

Basel, 4031, Switzerland

Location status: Recruiting

Location contact

Matthias Betz, Prof.

CONTACT

[email protected]

0041 61 556 56 54

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • BMI 18.5 to 25 kg/m2
  • Able to give informed consent as documented by signature
  • Moderate caffeine consumption (1 to 3 cups of coffee per day)
  • Increase of EE in response to mild cold of ≥ 5% of REE

Exclusion criteria

  • Known hypersensitivity or allergy to caffeine
  • Concomitant medication other than prescription free analgesics (paracetamol and NSAID) and oral contraceptives
  • Other clinically significant concomitant disease states (e.g., renal failure, hepatic dysfunction, cardiovascular disease, cardiac arrhythmia, hypertension, diabetes mellitus, hyper- or hypothyroidism)
  • History of depressive disorder or anxiety disorder
  • Smoker / habitual tobacco use
  • Habitual excessive alcohol use
  • Regular consumption of caffeine containing energy drinks
  • Weight change of >5% within 3 months prior to inclusion
  • Systolic blood pressure >140 mmHg and/or diastolic blood pressure > 95 mmHg.
  • Resting heart rate >90 bpm
  • Hypersensitivity to cold (e.g. Raynaud syndrome)
  • Known or suspected non-compliance, drug or alcohol abuse
  • Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant.
  • Enrolment of the investigator, his/her family members, employees, and other dependent persons
  • Enrolment into another study using ionizing radiation within the previous 12 months.
  • Pregnancy or lactation

Treatment and study plan

Caffeine (200 mg)

Drug

single dose of 200mg caffeine orally in study visit A

Placebo

Drug

single dose of 1 tablet Placebo in study visit B

Primary outcomes

  1. BAT SUVmean

    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

Secondary outcomes

  1. BAT SUVmax

    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

  2. BAT Volume

    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.

  3. Cold induced thermogenesis (CIT)

    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.

  4. Resting energy expenditure (REE)

    Time frame: immediately after the intervention (caffeine or placebo)

    REE during warm conditions and at the end of cold exposure.

  5. Respiratory exchange ratio (RER):

    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.

  6. Skin temperature

    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

  7. Metabolom and Lipidome profile

    Time frame: immediately after the intervention (caffeine or placebo)

    Plasma metabolome and lipidome profiles.

  8. Caffeine and its metabolites

    Time frame: immediately after the intervention (caffeine or placebo)

    Plasma caffeine and its metabolites.

Study contacts

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

Jaël Senn, MD

CONTACT

[email protected]

0041 61 328 70 79

Matthias Betz, Prof.

CONTACT

[email protected]

0041 61 556 56 54

Sponsors and collaborators

Lead sponsor

University Hospital, Basel, Switzerland

Other

Registry information

Acronym: ACROBAT

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
May 18, 2025
Registry last updated
Jan 23, 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.

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