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Completed

NCT Number: NCT06556277

Acute Consequences of Glucocorticoid Secretion in Overweight and Obese Individuals During Maximum Calorie Intake

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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Key information

Age range

18 year–50 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital Basel

Basel, Canton of Basel-City, 4031, Switzerland

About this study

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)

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Males aged 18 to 50 years
  • BMI≥ 25 kg/m² with a stable weight within past three months before study initiation

Exclusion criteria

  • Any severe acute or chronic disease, including diabetes mellitus type 2
  • Intake of GLP-1 agonists or hormone therapy
  • Hypercortisolism
  • Casual smoking (more than 6 cigarettes per day)
  • Frequent, heavy alcohol consumption (more than 30g/day)
  • Frequent, heavy caffeine consumption (more than 4 caffeinated drinks/day)
  • Regular physical exercise (more than 4hrs per week)
  • Shift work
  • Participation in an investigational drug trial within the past two months
  • Intake of any steroid-containing drugs, including topical steroids and inhalers, within 4 weeks of the study initiation
  • Known allergy to metyrapone
  • Inability or unwillingness to provide informed consent

Treatment and study plan

Metyrapone And Hydrocortisone

Drug

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

Placebo

Drug

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

Primary outcomes

  1. Total body fat

    Time frame: Two 7-day intervention periods

    Change in total body fat assessed with a Dual-Energy-X-Ray-Absorptiometry (DXA)

Secondary outcomes

  1. Total lean mass

    Time frame: Two 7-day intervention periods

    Change in total lean mass assessed with DXA

  2. Insulin sensitivity

    Time frame: Two 7-day intervention periods

    Change in insulin sensitivity assessed with a mixed meal tolerance test

  3. Glucose

    Time frame: Two 7-day intervention periods

    Change in Glucose assessed with a mixed meal tolerance test

  4. Insulin

    Time frame: Two 7-day intervention periods

    Change in Insulin assessed with a mixed meal tolerance test

  5. C-peptide

    Time frame: Two 7-day intervention periods

    Change in C-peptide assessed with a mixed meal tolerance test

  6. Energy expenditure

    Time frame: Two 7-day intervention periods

    Basal metabolic rate measured with indirect calorimetryy

  7. Substrate utilization

    Time frame: Two 7-day intervention periods

    Respiratory quotient assessed with indirect calorimetry

  8. Systolic and diastolic blood pressure

    Time frame: Two 7-day intervention periods

    Assessment of blood pressure with a standard blood pressure monitor.

  9. Weight

    Time frame: Two 7-day intervention periods

    Measurement of weight with a standard scale

  10. Lipids (mmol/l) ((total cholesterol, LDL-cholesterol, HDL-cholesterol and triglycerides)

    Time frame: Two 7-day intervention periods

    Blood sample

  11. Immune cells (peripheral blood mononuclear cells)

    Time frame: Two 7-day intervention periods

    Blood sample

  12. Satiation

    Time frame: Two 7-day intervention periods

    Amount of food intake with ad libitum buffet

  13. Satiety

    Time frame: Two 7-day intervention periods

    Appetite rating with visual analogue scale (VAS) from 0mm-100mm (0mm=not at all and 100mm=extreme)

  14. Motivation

    Time frame: Two 7-day intervention periods

    Motivation to eat measured with a speed clicking test

  15. IL-6 (Inflammatory markers)

    Time frame: Two 7-day intervention periods

    Blood sample

  16. IL-1RA (Inflammatory markers)

    Time frame: Two 7-day intervention periods

    Blood sample

  17. IL-8 (Inflammatory markers)

    Time frame: Two 7-day intervention periods

    Blood sample

  18. CRP (Inflammatory markers)

    Time frame: Two 7-day intervention periods

    Blood sample

  19. Thyroid hormones

    Time frame: Two 7-day intervention periods

    Blood sample

  20. Growth hormone

    Time frame: Two 7-day intervention periods

    Blood sample

  21. IGF1

    Time frame: Two 7-day intervention periods

    Blood sample

  22. Catecholamines

    Time frame: Two 7-day intervention periods

    Blood sample

  23. GLP-1

    Time frame: Two 7-day intervention periods

    Blood sample

  24. GIP

    Time frame: Two 7-day intervention periods

    Blood sample

  25. Glucagon

    Time frame: Two 7-day intervention periods

    Blood sample

  26. PYY

    Time frame: Two 7-day intervention periods

    Blood sample

  27. CCK

    Time frame: Two 7-day intervention periods

    Blood sample

  28. FGF21

    Time frame: Two 7-day intervention periods

    Blood sample

  29. Leptin

    Time frame: Two 7-day intervention periods

    Blood sample

  30. Ghrelin

    Time frame: Two 7-day intervention periods

    Blood sample

  31. GDF15

    Time frame: Two 7-day intervention periods

    Blood sample

  32. Cortisol

    Time frame: Two 7-day intervention periods

    Blood sample

  33. Aldosterone

    Time frame: Two 7-day intervention periods

    Blood sample

  34. Renin

    Time frame: Two 7-day intervention periods

    Blood sample

  35. ACTH

    Time frame: Two 7-day intervention periods

    Blood sample

  36. Pregnenolone

    Time frame: Two 7-day intervention periods

    Blood sample

  37. Progesterone

    Time frame: Two 7-day intervention periods

    Blood sample

  38. 11-deoxycorticosterone

    Time frame: Two 7-day intervention periods

    Blood sample

  39. Corticosterone

    Time frame: Two 7-day intervention periods

    Blood sample

  40. 18-hydroxycorticosterone

    Time frame: Two 7-day intervention periods

    Blood sample

  41. 17-hydroxypregnenolone

    Time frame: Two 7-day intervention periods

    Blood sample

  42. 17-hydroxyprogesterone

    Time frame: Two 7-day intervention periods

    Blood sample

  43. 11-deoxycortisol

    Time frame: Two 7-day intervention periods

    Blood sample

  44. Oxytocin

    Time frame: Two 7-day intervention periods

    Blood sample

Other outcomes

  1. Untargeted metabolomics of blood

    Time frame: Two 7-day intervention periods

    Blood sample

  2. Untargeted metabolomics of adipose tissue

    Time frame: Two 7-day intervention periods

    Adipose tissue sample

  3. Untargeted metabolomics of muscle

    Time frame: Two 7-day intervention periods

    Muscle tissue sample

  4. Gene expression analysis of adipose tissue

    Time frame: Two 7-day intervention periods

    Adipose tissue sample

  5. Gene expressions analysis of muscle tissue

    Time frame: Two 7-day intervention periods

    Muscle tissue sample

Sponsors and collaborators

Lead sponsor

Eleonora Seelig

Other

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Aug 16, 2024
Registry last updated
May 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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