NCT06511297Recruiting
Metabolic Control of Aging and Disease - the MetAGE Deep Phenotyping Cohort
Metabolic Control of Aging and Disease - the MetAGE Deep Phenotyping Cohort (Pro-Metage)
Source: ClinicalTrials.gov · Last updated 17 Feb 2026
Brief summary (registry, in English)
The goal of this prospective observational study is to identify and validate blood based aging biomarkers in relation to cardiometabolic phenotypes of young and old, female and male subjects with or without obesity. The main question is to gain insights into the interaction of obesity related metabolic alteration and aging, and the relevance of loss of metabolic control in the development of age-related diseases in order to build a foundation for targeted drug- and lifestyle interventions in future studies.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 650 (estimated)
- First submitted
- 9 Jul 2024
- Start date
- 5 May 2025
- Primary completion date
- 1 Jan 2035
- Lead sponsor
- Thomas Scherer
- Diseases
- Obesity
- NCT number
- NCT06511297
What you commit to
- Study type: Observational
- Planned participants: 650
- From 5 May 2025 to the primary completion date, 1 Jan 2035
- 2 sites 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
- drug abuse, alcohol \> 15 drinks/week
- Metal implants that prohibit 3T MRI
- drug abuse, alcohol \> 15 drinks/week
- Metal implants that prohibit 3T MRI
- drug abuse, alcohol \> 15 drinks/week
- Metal implants that prohibit 3T MRI
- No previous heart failure, cardiovascular disease, immunosuppressive therapies, chronic inflammatory diseases and active oncologic conditions up until the age of 35 years.
- drug abuse, alcohol \> 15 drinks/week
- Metal implants that prohibit 3T MRI
- No previous heart failure, cardiovascular disease, immunosuppressive therapies, chronic inflammatory diseases and active oncologic conditions up until the age of 35 years.
- Metal implants that prohibit 3T MRI
Other illness
- Highly physical active (i.e. \> 5 times sporting activity / week with moderate to high intensity \[heart rate 140 - 200bpm\])
- Clinically significant metabolic or endocrine disorders
- Heart failure, cardiovascular disease, immunosuppressive therapies, chronic inflammatory diseases and active oncologic conditions
- Highly physical active (i.e. \> 5 times sporting activity / week with moderate to high intensity \[heart rate 140 - 200bpm\])
- Clinically significant metabolic or endocrine disorders
- Heart failure, cardiovascular disease, immunosuppressive therapies, chronic inflammatory diseases and active oncologic conditions
- Highly physical active (i.e. \> 5 times sporting activity / week with moderate to high intensity \[heart rate 140 - 200bpm\])
- Diabetes, overt hypo/hyperthyroidism
- Life-threatening conditions with a life expectancy of less than 1 year or any other condition that would jeopardize proband safety/adherence while participating in this trial.
- Group 4 - Overweight, older adults (n = 150)
- Diabetes, overt hypo/hyperthyroidism
- Clinically significant cognitive impairment compromising study adherence
- Life-threatening conditions with a life expectancy of less than 1 year or any other condition that would jeopardize proband safety/adherence while participating in this trial.
Lab values
- Known severe cardiovascular diseases (i.e. PAD IIa or higher, advanced heart failure = left ventricular ejection fraction (LVEF) \< 35% or NYHA Class III-IV)
Age
- Life-threatening conditions with a life expectancy of less than 1 year or any other condition that would jeopardize proband safety/adherence while participating in this trial.
- Group 5 - "healthy" Nonagenerians Age ≥ 90 (n = 50)
Other
- Group 1 - Lean, young adults (n = 150)
- Special diets (i.e. ketogenic diet and time-restricted eating)
- Claustrophobia
- Pregnancy or breastfeeding
- Group 2 - Overweight, young adults (n = 150)
- Special diets (i.e. ketogenic diet and time-restricted eating)
- Active anti-obesity treatment (e.g. glucagon-like peptide 1 (GLP-1) analogues, polyagonists, naltrexone and bupropion)
- Claustrophobia
- Pregnancy or breastfeeding
- Group 3 - Lean, older adults (n = 150)
- Special diets (i.e. ketogenic diet and time-restricted eating)
- Claustrophobia
- Special diets (i.e. ketogenic diet and time-restricted eating)
- Active anti-obesity treatment (e.g. GLP-1 analogues, polyagonists, naltrexone and bupropion)
- Claustrophobia
- Claustrophobia
Who the study is looking for
- Group 1 - Lean, young adults (n = 150)
- Age 18 - 35 years
- Body mass index (BMI) ≥ 18.5 and ≤ 24.9 kg/m2 (≥ 12 months)
- Group 2 - Overweight, young adults (n = 150)
- Age 18 - 35 years
- BMI ≥ 28kg/m2 (≥ 12 months)
- Group 3 - Lean, older adults (n = 150)
- Age ≥ 60 years
- BMI ≥ 18.5 and ≤ 24.9 kg/m2 (≥ 3 years)
- Group 4 - Overweight, older adults (n = 150)
- Age ≥ 60 years
- BMI ≥ 28 kg/m2 (≥ 3 years)
- Subgroup A (n=75): with pre-existent cardiovascular disease defined as: history of myocardial infarction or evidence of coronary artery disease irrespective of revascularization status or history of ischemic or hemorrhagic stroke or presence of peripheral artery disease or heart failure with preserved ejection fraction (NYHA Class I-II).
- Subgroup B (n=75): without pre-existent cardiovascular disease
- Group 5 - Nonagenerians Age ≥ 90 (n = 50)
- Age ≥ 90 years
- BMI ≥ 18.5 kg/m2 (≥ 3 years)
Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Medical University of Graz Coordinator of this site? Confirm its status | Graz | Austria | Recruiting |
| Medical University of Vienna Coordinator of this site? Confirm its status | Vienna | Austria | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.