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Effect of spironolactone on brown fat activity in adult humans

Phase 4
Completed
Conditions
Obesity
Diet and Nutrition - Obesity
Registration Number
ACTRN12614001112651
Lead Sponsor
Professor Ken Ho
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
10
Inclusion Criteria

healthy adults aged 18-50 years old, BMI<35

Exclusion Criteria

Pregnancy
eGFR <60

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Brown Fat volume changes on 18FDG-PET-CT scan[after two weeks of placebo and after two weeks of spironolactone];Brown fat activity changes on PET-CT[after two weeks of placebo and after two weeks of spironolactone]
Secondary Outcome Measures
NameTimeMethod
Changes in resting energy expenditure using indirect calorimetry<br>[after two weeks of placebo and after two weeks of spironolactone];Changes in diet-induced thermogenesis using indirect calorimetry<br>[after two weeks of placebo and after two weeks of spironolactone]
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