Mirabegron and Physiological Function in Cold Environments

Completed · Phase 1/Phase 2 · Has a placebo group

Conditions studied: Resting Energy Expenditure, Thermogenesis, Brown Adipose Tissue

In brief

Many Navy diving operations are performed in cold water. Despite technical advances to improve thermal protection for cold water diving, these applications are cumbersome and do not provide complete thermal protection as thermal discomfort is subjectively reported by many Navy divers. Brown adipose tissue is highly thermogenic in humans. Therefore, activation of brown adipose tissue might improve cold water tolerance and lower thermal discomfort during cold water diving operations. Mirabegron is a beta-3-adrenergic receptor agonist that is used to treat overactive bladder. Beta-3-adrenergic receptors are located on the urinary bladder, gallbladder and brown adipose tissue. Recent evidence has demonstrated that acute mirabegron administration increases thermogenesis for \~3 hours in humans. However, it is currently not known which dose of mirabegron can increase thermogenesis for longer durations. It is also not known if mirabegron administration can improve cold water tolerance and thermal discomfort during cold water immersion. Finally, it is not known if mirabegron can increase thermogenesis during sympathetic stimulation. This project will fill these knowledge gaps by determining which dose of mirabegron administration will increase thermogenesis during 6 hours of a mild cold stress challenge. This study is part of a collection of studies that will show if mirabegron is a potential ergogenic aid that can be used to improve cold water tolerance in Navy divers which will ultimately improve the likelihood of successful missions.

Key facts

Study ID

NCT04766021

Run by

Indiana University

People needed

30

Starts

2021-11-30

Expected to finish

2023-04-27

Last updated by the study team

2024-07-12

Who can join

Age: 18 and older, up to 40. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Men and women
• 18-40 years old
• Participate in 150 minutes or more of at least moderate intensity exercise per week during the previous 2 years

You may not qualify if…

• diagnosed autonomic disease
• diagnosed cardiovascular disease
• diagnosed metabolic disease
• diagnosed neurologic disease
• diagnosed endocrine disease
• diagnosed respiratory disease
• diagnosed liver dysfunction
• diagnosed kidney dysfunction
• Women who are pregnant or breastfeeding
• Individuals currently taking a medication (with the exception of birth control, including hormonal contraception) that cannot be safely discontinued for 5 biological half-lifes prior to each study visit based on consultation with the study physician.
• Current tobacco or electronic cigarette use or consistent use within the last 1 year

Where it is running

• Indiana University — Bloomington, Indiana, United States

Full record on ClinicalTrials.gov

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