University Hospital Basel
Basel, Canton of Basel-City, 4031, Switzerland
NCT Number: NCT05167084
In a randomized, cross-over study, 20 healthy volunteers 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 and autonomic parameters will be compared to reveal, whether GCs mediate the physiological adaptions to excessive food intake.
Understanding acute effects of GCs upon food intake is critical, since repetitive disruptions of GC secretion may become harmful in chronic conditions.
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Notify Me18 year–40 year
Male
Interventional
Early Phase 1
Basel, Canton of Basel-City, 4031, Switzerland
Obesity is one of the most serious health problems of the 21st century. To understand how we regulate our body weight is crucial for developing new treatment targets. Even though body mass index of populations is increasing, the body weight of adults is usually kept stable over time. Indeed, acute excessive food intake triggers a set of adaptions in order to prevent weight gain. The signal that triggers these beneficial adaptions is still unknown. Glucocorticoid (GC) secretion increases with acute food intake and many physiological adaptions to overfeeding coincide with classical glucocorticoid actions. The investigators therefore hypothesize that GCs are the signal that prevents weight gain during acute overfeeding.
The objective of this project is to test whether food-induced GCs represent the physiological signal that defends against weight gain.
The primary objective is to investigate whether reduction in insulin sensitivity is abolished with the block and replace therapy.
Secondary objectives are to investigate whether suppression of GC secretion during excessive food intake impairs the activation of sympathetic nervous system, satiety, satiation, energy expenditure, substrate utilization, blood pressure, secretion of neuroendocrine hormones, lipids and immune cells.
This is a double-blind, randomized, placebo-controlled cross-over study. After screening, subjects will be randomized to two crossover 8-day study periods with a washout period of 28 days:
A) Participants will receive hydrocortisone 19.9 mg/d subcutaneously via a pump in a pulsed fashion (eight times/day) and metyrapone per os (starting with a dose of 500 mg/d on day 1 to 2500mg/d on day 4, and then will be kept constant until day 8)
B) Participants will receive placebo (0,9% NaCl solution) 19.9 mg/d subcutaneously via a pump in a pulsed fashion and placebo pills per os (starting with a dose of 500 mg/d on day 1 to 2500mg/d on day 4, and then will be kept constant until day 8)
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
During one phase of the study: Metyrapone (pills of 250mg) on full stomach: Day 1 0-1-1, day 2 1-2-2, day 3 2-2-3 day 4 3-3-4 day 5 3-3-4 day 6 3-3-4 day 7 3-3-4 day 8 3-0-0
During another phase of the study: identical looking placebo pills starting Day 1 0-1-1, day 2 1-2-2, day 3 2-2-3 day 4 3-3-4 day 5 3-3-4 day 6 3-3-4 day 7 3-3-4 day 8 3-0-0
Hydrocortisone will be delivered subcutaneously via a pump in a pulsed fashion with a flow rate of 10μl/s from day 1 to day 8 in a total daily dose of 19.9mg
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 8
Time frame: Two 8-day intervention periods
Change in insulin sensitivity assessed with a mixed meal tolerance test
Time frame: Two 8-day intervention periods
Blood sample
Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
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Time frame: Two 8-day intervention periods
Blood Sample
Time frame: Two 8-day intervention periods
Heart rate variability analysis
Time frame: Two 8-day intervention periods
Assessment of blood pressure with a standard blood pressure monitor.
Time frame: Two 8-day intervention periods
Measurement of weight with a standard scale
Time frame: Two 8-day intervention periods
Basal metabolic rate measured with indirect calorimetry
Time frame: Two 8-day intervention periods
Respiratory quotient assessed with indirect calorimetry
Time frame: Two 8-day intervention periods
Appetite rating with visual analogue scale (VAS) from 0mm-100mm (0mm=not at all and 100mm=extreme)
Time frame: Two 8-day intervention periods
Amount of food intake with ad libitum buffet
Time frame: Two 8-day intervention periods
Blood Sample
Time frame: Two 8-day intervention periods
Blood Sample
Time frame: Two 8-day intervention periods
Blood Sample
Time frame: Two 8-day intervention periods
Blood Sample
Time frame: Two 8-day intervention periods
Metabolomics will be performed in blood plasma
Eleonora Seelig
Other
Acute Consequences Of Food-induced Glucocorticoid Secretion In Healthy Individuals - A Double-blind, Randomized, Placebo-controlled Cross-over Study
Acronym: Gluco-Feed
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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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