Effect of spironolactone on brown fat activity in adult humans
Phase 4
Completed
- Conditions
- ObesityDiet 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
Name Time Method 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
Name Time Method 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]