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Beta-3 Adrenergic Agonist

Mirabegron for Temperature Regulation

Phase < 1
Waitlist Available
Led By Christopher Bell, Ph.D.
Research Sponsored by Christopher Bell
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Age 18-40 years
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up immediately after each infusion.
Awards & highlights

Study Summary

This trial found that taking mirabegron can increase fat-burning and improve glucose regulation, possibly changing muscle structure.

Who is the study for?
This trial is for healthy adults aged 18-40 who exercise regularly (over 150 minutes of moderate intensity weekly) for the past two years. It's not suitable for pregnant or breastfeeding individuals, those with heart, lung, metabolic diseases like diabetes, liver/kidney problems, or on certain medications that don't mix well with Mirabegron.Check my eligibility
What is being tested?
The study tests if Myrbetriq (Mirabegron), a drug normally used to treat overactive bladder, can increase body heat produced by brown fat compared to a placebo. The goal is also to see if it has long-term benefits on glucose regulation and muscle changes.See study design
What are the potential side effects?
Possible side effects of Mirabegron include increased blood pressure, urinary tract infections, headaches, dizziness, nausea and could potentially interact unfavorably with other drugs.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am between 18 and 40 years old.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~immediately after each infusion.
This trial's timeline: 3 weeks for screening, Varies for treatment, and immediately after each infusion. for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in core temperature measured via oral thermometer during each stage.
Change in metabolic rate compared to baseline during each stage as measured by indirect calorimetry
Change in temperature among the top 10% of hottest pixels as identified via thermal camera and FLIR research software in the supraclavicular region during each isoproterenol infusion.

Side effects data

From 2019 Phase 4 trial • 28 Patients • NCT02086188
7%
urinary tract infection
7%
asthma
7%
gastritis
7%
fatigue
7%
diarrhea
7%
headache
100%
80%
60%
40%
20%
0%
Study treatment Arm
Placebo
Mirabegron

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: Mirabegron + IsoproterenolExperimental Treatment1 Intervention
100mg oral + Isoproterenol IV Infusion; 3 doses, 6, 12, 24ng/ kg Fat Free Mass
Group II: Placebo + IsoproterenolPlacebo Group1 Intervention
Empty Capsule + Isoproterenol IV Infusion; 3 doses, 6, 12, 24ng/ kg Fat Free Mass

Find a Location

Who is running the clinical trial?

Indiana UniversityOTHER
980 Previous Clinical Trials
983,142 Total Patients Enrolled
Christopher BellLead Sponsor
7 Previous Clinical Trials
179 Total Patients Enrolled
Christopher Bell, Ph.D.Principal InvestigatorColorado State University
1 Previous Clinical Trials
62 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Does this experiment open its doors to those of advanced age?

"This research project is seeking individuals between the legal age of consent and 40 years old."

Answered by AI

Do I meet the criteria to join this investigation?

"The candidate selection criteria for this trial stipulates that those who wish to participate should have thermoregulatory control and be between the ages of 18-40. 15 people are needed in total."

Answered by AI

Is this research protocol currently open for enrollment?

"Correct. Per the information published on clinicaltrials.gov, this research initiative is actively enlisting patients. It was first posted on April 27th 2023 and has been updated as recently as August 21st of the same year. The study requires 15 volunteers from a single site to take part in it."

Answered by AI

How many participants are engaged in this research experiment?

"Affirmative. According to the information provided on clinicaltrials.gov, this research endeavour is actively recruiting participants, with 15 people needed from 1 site. The study was initially posted on April 27th 2023 and then updated most recently on August 21st 2023."

Answered by AI
~9 spots leftby Apr 2025