University Hospital Basel
Basel, Canton of Basel-City, 4031, Switzerland
NCT Number: NCT06556277
The investigator aim to understand whether food-induced glucocorticoids influence fat mass in overweight and obese people.
In a randomized, cross-over study, 23 overweight and obese volunteers will receive a block and replace therapy that mimics physiological glucocorticoid (GC) rhythm (metyrapone plus hydrocortisone) or placebo. Participants will undergo two identical overfeeding periods with each treatment. With the block and replace therapy food-induced GC peak will be suppressed. Metabolic and immunological parameters will be compared to reveal the effects of GCs during excessive overfeeding, particularly to understand changes in body fat.
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Notify Me18 year–50 year
Male
Interventional
Not applicable
Basel, Canton of Basel-City, 4031, Switzerland
Obesity is one of the most serious health problems of the 21st century, and new therapies are urgently needed.
Glucocorticoids (GCs) increase with acute food intake. Several clinical studies have found that glucocorticoids contribute to common obesity, but the underlying mechanisms remain unknown. Here, the investigator aim to understand whether GCs influence the total body fat in obese and overweight study participants during excessive overfeeding.
In a randomized, cross-over study, 23 overweight and obese individuals will receive a block and replace therapy that mimics physiological GC rhythm (Metyrapone plus hydrocortisone) or placebo. Participants will undergo two identical overfeeding periods with each treatment. With the block and replace therapy, food-induced GC peak will be suppressed. Metabolic, autonomic, and immunological parameters will be compared.
A) Participants will receive hydrocortisone 19.9mg/d day 1 to day 6 and 12mg on day 7 subcutaneously via a pump in a pulsed fashion (eight times/day) and metyrapone per os (starting with a dose of 750mg/d on day 1 to 2500mg on day 3, which will be kept constant until day 6 and then reduced to 750mg on day 7)
B) Participants will receive placebo (0,9% NaCl solution) 19.9mg/d day 1 to day 6 and 12mg on day 7 subcutaneously via a pump in a pulsed fashion (eight times/day) and placebo pills per os (starting with a dose of 750mg/d on day 1 to 2500mg on day 3, which will be kept constant until day 6 and then reduced to 750mg on day 7)
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Drug: Metyrapone 250 mg Oral Tablets
During one phase of the study: Metyrapone (pills of 250mg) on full stomach: Day 1 0-1-2, day 2 1-2-2, day 3 3-3-4 day 4 3-3-4 day 5 3-3-4 day 6 3-3-4 day 7 3-0-0
Drug: Hydrocortisone 19,9mg/12mg s.c., pulsatile with a flow rate of 10μl/s
Hydrocortisone will be delivered subcutaneously via a pump in a pulsed fashion with a flow rate of 10μl/s from day 1 to day 6 in a total daily dose of 19.9mg and 12mg on day 7
Drug: Placebo 250 mg Tablets
During another phase of the study: identical looking placebo pills starting Day 1 During one phase of the study: Metyrapone (pills of 250mg) on full stomach: Day 1 0-1-2, day 2 1-2-2, day 3 3-3-4 day 4 3-3-4 day 5 3-3-4 day 6 3-3-4 day 7 3-0-0
Drug: Placebo (0,9% NaCl solution)
Placebo (0,9% NaCl solution) 19.9 mg/d subcutaneously via a pump in a pulsed fashion with a flow rate of 10μl/s from day 1 to day 6 and 12mg on day 7
Time frame: Two 7-day intervention periods
Change in total body fat assessed with a Dual-Energy-X-Ray-Absorptiometry (DXA)
Time frame: Two 7-day intervention periods
Change in total lean mass assessed with DXA
Time frame: Two 7-day intervention periods
Change in insulin sensitivity assessed with a mixed meal tolerance test
Time frame: Two 7-day intervention periods
Change in Glucose assessed with a mixed meal tolerance test
Time frame: Two 7-day intervention periods
Change in Insulin assessed with a mixed meal tolerance test
Time frame: Two 7-day intervention periods
Change in C-peptide assessed with a mixed meal tolerance test
Time frame: Two 7-day intervention periods
Basal metabolic rate measured with indirect calorimetryy
Time frame: Two 7-day intervention periods
Respiratory quotient assessed with indirect calorimetry
Time frame: Two 7-day intervention periods
Assessment of blood pressure with a standard blood pressure monitor.
Time frame: Two 7-day intervention periods
Measurement of weight with a standard scale
Time frame: Two 7-day intervention periods
Blood sample
Time frame: Two 7-day intervention periods
Blood sample
Time frame: Two 7-day intervention periods
Amount of food intake with ad libitum buffet
Time frame: Two 7-day intervention periods
Appetite rating with visual analogue scale (VAS) from 0mm-100mm (0mm=not at all and 100mm=extreme)
Time frame: Two 7-day intervention periods
Motivation to eat measured with a speed clicking test
Time frame: Two 7-day intervention periods
Blood sample
Time frame: Two 7-day intervention periods
Blood sample
Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
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Time frame: Two 7-day intervention periods
Blood sample
Time frame: Two 7-day intervention periods
Adipose tissue sample
Time frame: Two 7-day intervention periods
Muscle tissue sample
Time frame: Two 7-day intervention periods
Adipose tissue sample
Time frame: Two 7-day intervention periods
Muscle tissue sample
Eleonora Seelig
Other
Acute Consequences of Glucocorticoid Secretion in Overweight and Obese Individuals During Maximum Calorie Intake: a Double-blind, Randomized, Placebo-controlled, Cross-over Study
Acronym: Gluco-Max
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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