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Recruiting NCT07048405

NCT07048405 Intermittent Cold Exposure and Brown Adipose Tissue Hyperplasia

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Clinical Trial Summary
NCT ID NCT07048405
Status Recruiting
Phase
Sponsor University of Edinburgh
Condition Brown Adipose Tissue
Study Type INTERVENTIONAL
Enrollment 12 participants
Start Date 2025-05-01
Primary Completion 2026-07

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 40 Years
Study Type INTERVENTIONAL
Interventions
CoolingBiopsiesInjection of 18F-FDG

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 12 participants in total. It began in 2025-05-01 with a primary completion date of 2026-07.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This clinical trial explores how repeated short-term cold exposure impacts the molecular and physiological function of brown adipose tissue (BAT), a thermogenic organ associated with improved cardiometabolic health. While intermittent cold exposure has been shown to increase BAT activity and mass, as measured by fluorodeoxyglucose (18F-FDG) uptake on positron emission tomography/computed tomography (PET/CT) scans, the molecular adaptations within BAT and other thermogenic tissues including skeletal muscle and white adipose tissue (WAT) remain poorly understood. Healthy adults aged 18 to 40 years (6 males and 6 females) will participate in a 10-day cold acclimation protocol (2 hours per day using water-perfused cooling blankets). The primary objective is to determine how cold exposure alters cellular heterogeneity and gene expression in BAT, WAT, and skeletal muscle. Participants will undergo baseline assessments, including measurements of energy expenditure, core and skin temperature, muscle activity, and blood sampling, each performed in both warm and cold conditions. These assessments will be followed by dynamic total-body PET/CT imaging during cold exposure and tissue biopsies from BAT, subcutaneous WAT, and skeletal muscle. These procedures will be repeated after the cold acclimation protocol to evaluate physiological and molecular changes. Additional outcomes include changes in energy expenditure, cold tolerance, and immune cell responses induced by cold exposure.

Eligibility Criteria

Inclusion Criteria: * Aged 18-40 years * Body mass index 18.5-25 kg/m2 * Weight change of less than 5% in the past 6 months * No acute or chronic medical conditions * On no regular medications (other than contraceptives in female participants) * No claustrophobia * Alcohol intake ≤14 units/ week * Screening blood tests within acceptable limits (of no clinical significance) * Not currently pregnant, lactating or breastfeeding (female participants only) * Ability to provide informed consent. Exclusion Criteria: * Not meeting inclusion criteria * Contra-indication to PET/CT scan * Allergy to local anaesthetic

Contact & Investigator

Central Contact

María Paula Huertas Caycedo

✉ m.p.huertas-caycedo@sms.ed.ac.uk

📞 01312429196

Frequently Asked Questions

Who can join the NCT07048405 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 40 Years, studying Brown Adipose Tissue. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07048405 currently recruiting?

Yes, NCT07048405 is actively recruiting participants. Contact the research team at m.p.huertas-caycedo@sms.ed.ac.uk for enrollment information.

Where is the NCT07048405 trial being conducted?

This trial is being conducted at Edinburgh, United Kingdom.

Who is sponsoring the NCT07048405 clinical trial?

NCT07048405 is sponsored by University of Edinburgh. The trial plans to enroll 12 participants.

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