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NCT06556277Completed

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

Acute Consequences of Glucocorticoid Secretion in Overweight and Obese Individuals During Maximum Calorie Intake: a Double-blind, Randomized, Placebo-controlled, Cross-over Study

Source: ClinicalTrials.gov · Last updated 22 May 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
23 (actual)
First submitted
17 Jul 2024
Start date
1 Sept 2024
Primary completion date
25 Feb 2026
Lead sponsor
Eleonora Seelig
Diseases
Obesity
NCT number
NCT06556277

What you commit to

  • Study type: Interventional
  • Participants enrolled: 23
  • From 1 Sept 2024 to the primary completion date, 25 Feb 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Intake of GLP-1 agonists or hormone therapy
  • 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

Other illness

  • Any severe acute or chronic disease, including diabetes mellitus type 2
  • Known allergy to metyrapone

Other

  • 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
  • Inability or unwillingness to provide informed consent

Who the study is looking for

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

Age in the registry: 18 years to 50 years · Sex: Male · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Hospital Basel
Coordinator of this site? Confirm its status
BaselSwitzerlandUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.