Effect of 4-week Dihydrocapsiate Ingestion on Resting Metabolic Rate
Status: | Completed |
---|---|
Conditions: | Obesity Weight Loss |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | 20 - 60 |
Updated: | 4/21/2016 |
Start Date: | July 2008 |
End Date: | December 2014 |
Effect of 4-week Dihydrocapsiate Ingestion on Resting Metabolic Rate: A Double-blind Randomized Parallel Arm Study
A 4 week intake of drug to find a natural substance that may modify energy balance and may
enhance health in combination with lifestyle changes with possible decrease in body weight.
enhance health in combination with lifestyle changes with possible decrease in body weight.
This study is a double-blind, placebo-controlled, single center, randomized, parallel arm
clinical trial to test the impact of Dihydrocapsiate (placebo, 3 and 9 mg/d) ingested for 4
weeks on resting metabolic rate and fat oxidation measured by indirect calorimetry.
clinical trial to test the impact of Dihydrocapsiate (placebo, 3 and 9 mg/d) ingested for 4
weeks on resting metabolic rate and fat oxidation measured by indirect calorimetry.
Inclusion Criteria:
- Men between 20-60 years old
- Healthy as assessed by medical history and standard medical exam
- Weight-stable
- Body mass index of 25 to 34.9 kg/m2
- Non-smoker
- Sedentary lifestyle: not being physically active grater than 3 days/week for 20 min
each time for the previous 6 months, and not participating in regular resistance
exercise.
Exclusion Criteria:
- Subjects enrolled in a diet to increase or decrease body weight
- Special diet or food aversiions to common foods
- Has allergy to chilli pepper
- Eating chilli peppers on a daily basis
- Usually consuming more than 2 cups of tea or coffee/day
- Usually consuming more than 4 cans of caffeinated soft drinks a day
- Usually consuming more than 3 standard alcohol drinks/day
- Regular use of medications (weight loss drugs, drugs affecting energy metabolism,
drugs for depression)
- Usual intake of illicit substances
- Claustrophobia
- Participating or having participated in another clinical trial during the last 4
weeks prior to the beginning of this study
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