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Completed

NCT Number: NCT05167084

Acute Consequences Of Food-induced Glucocorticoid Secretion In Healthy Individuals

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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Key information

Age range

18 year–40 year

Sex eligibility

Male

Study type

Interventional

Phase

Early Phase 1

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. 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)

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • BMI 18.5 - 25 kg/m2

Exclusion criteria

  • Previous medical history for any chronic condition in the last three months, active disease or abnormal physical examination as verified by a qualified physician.
  • Casual smoking (>6 cigarettes per day)
  • Frequent, heavy alcohol consumption (>30g/day)
  • Frequent, heavy caffeine consumption (>4 caffeinated drinks/day)
  • Regular physical exercise (>4hrs per week)
  • Shift workers
  • Participation in an investigational drug trail within the past two months
  • Intake of any drugs (prescribed, over the counter or recreational) including topical steroids and inhalers, within 48 hours of the study initiation
  • Known allergy to metyrapone
  • Inability or unwillingness to provide informed consent

Treatment and study plan

Metyrapone 250 mg Oral Tablets

Drug

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

Placebo 250 mg Tablets

Drug

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 19,9mg s.c., pulsatile with a flow rate of 10μl/s

Drug

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)

Drug

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

Primary outcomes

  1. Insulin sensitivity

    Time frame: Two 8-day intervention periods

    Change in insulin sensitivity assessed with a mixed meal tolerance test

Secondary outcomes

  1. Cortisol (nmol/l) total and free

    Time frame: Two 8-day intervention periods

    Blood sample

  2. Renin

    Time frame: Two 8-day intervention periods

    Blood Sample

  3. Aldosterone (Adrenal Steroid Hormones)

    Time frame: Two 8-day intervention periods

    Blood Sample

  4. Pregnenolon (Adrenal Steroid Hormones)

    Time frame: Two 8-day intervention periods

    Blood Sample

  5. Progesteron (Adrenal Steroid Hormones)

    Time frame: Two 8-day intervention periods

    Blood Sample

  6. 11-Deoxycorticosteron (Adrenal Steroid Hormones)

    Time frame: Two 8-day intervention periods

    Blood Sample

  7. Corticosteron (Adrenal Steroid Hormones)

    Time frame: Two 8-day intervention periods

    Blood Sample

  8. 18-Hydroxycorticosteron (Adrenal Steroid Hormones)

    Time frame: Two 8-day intervention periods

    Blood Sample

  9. 17-Hydroxypregnenolon (Adrenal Steroid Hormones)

    Time frame: Two 8-day intervention periods

    Blood Sample

  10. 17-Hydroxyprogesteron (Adrenal Steroid Hormones)

    Time frame: Two 8-day intervention periods

    Blood Sample

  11. 11-Deoxycortisol (Adrenal Steroid Hormones)

    Time frame: Two 8-day intervention periods

    Blood Sample

  12. GLP-1 (nmol/l)

    Time frame: Two 8-day intervention periods

    Blood sample

  13. GIP (nmol/l)

    Time frame: Two 8-day intervention periods

    Blood Sample

  14. PYY (pg/ml)

    Time frame: Two 8-day intervention periods

    Blood Sample

  15. T3 (nmol/l)

    Time frame: Two 8-day intervention periods

    Blood Sample

  16. T4 (nmol/l)

    Time frame: Two 8-day intervention periods

    Blood Sample

  17. TSH (mIU/l)

    Time frame: Two 8-day intervention periods

    Blood Sample

  18. HGH (mIU/l)

    Time frame: Two 8-day intervention periods

    Blood Sample

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

    Time frame: Two 8-day intervention periods

    Blood Sample

  20. GDF-15 (pg/mL)

    Time frame: Two 8-day intervention periods

    Blood Sample

  21. Sympathetic nervous system activity

    Time frame: Two 8-day intervention periods

    Heart rate variability analysis

  22. Systolic and diastolic blood pressure

    Time frame: Two 8-day intervention periods

    Assessment of blood pressure with a standard blood pressure monitor.

  23. Weight

    Time frame: Two 8-day intervention periods

    Measurement of weight with a standard scale

  24. Energy expenditure

    Time frame: Two 8-day intervention periods

    Basal metabolic rate measured with indirect calorimetry

  25. Substrate utilisation

    Time frame: Two 8-day intervention periods

    Respiratory quotient assessed with indirect calorimetry

  26. Satiety

    Time frame: Two 8-day intervention periods

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

  27. Satiation

    Time frame: Two 8-day intervention periods

    Amount of food intake with ad libitum buffet

Other outcomes

  1. IL-6 (Inflammatory markers)

    Time frame: Two 8-day intervention periods

    Blood Sample

  2. IL-1RA (Inflammatory markers)

    Time frame: Two 8-day intervention periods

    Blood Sample

  3. IL-8 (Inflammatory markers)

    Time frame: Two 8-day intervention periods

    Blood Sample

  4. CRP (Inflammatory markers)

    Time frame: Two 8-day intervention periods

    Blood Sample

  5. Metabolomics

    Time frame: Two 8-day intervention periods

    Metabolomics will be performed in blood plasma

Sponsors and collaborators

Lead sponsor

Eleonora Seelig

Other

Registry information

Official study title

Acute Consequences Of Food-induced Glucocorticoid Secretion In Healthy Individuals - A Double-blind, Randomized, Placebo-controlled Cross-over Study

Acronym: Gluco-Feed

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Dec 22, 2021
Registry last updated
Aug 23, 2023

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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