Obesity Trial, Recruiting NCT01224886 Sponsor: University of Lausanne Condition: Obesity
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Obesity Trial, Recruiting

NCT01224886
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People between the ages of 60 and 80
  • People who are either very inactive (sedentary) or highly physically active and trained
  • People with a body mass index (a measure of body weight relative to height) between 18 and 40
  • People who do not smoke
  • People whose blood sugar levels are either normal or slightly higher than normal (but not high enough to be diagnosed as diabetes)
  • People who are willing and able to follow the study plan and requirements

Who may not be able to join:

  • People with health conditions that make moderate exercise unsafe, such as significant heart disease, problems with blood flow in the legs, uncontrolled high blood pressure, or nerve or joint conditions
  • People who have recently lost or gained a noticeable amount of weight
  • People who have been diagnosed with diabetes
  • People who take certain medications known to affect blood sugar levels, such as nicotinic acid (a form of vitamin B3 used as a drug) or steroid medications called glucocorticoids
  • People with severe anaemia (low red blood cells), significant problems with fats in the blood, or liver or kidney disease
  • People with a recent history of cancer
  • People with an underactive thyroid (hypothyroidism)
  • People who have recently used hormone replacement therapy
  • People with a known allergy to lidocaine or similar local anaesthetic medicines
  • People who have had a positive stress test result (a test that checks how the heart responds to physical activity)
  • People with current issues related to alcohol or substance use

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Francesca Amati, MD,PhD, University of Lausanne

Phone: +41 21 692 5552

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
University of Lausanne
Registry
ClinicalTrials.gov
Start date
1 October 2010
Est. completion
1 December 2028

Where this trial is recruiting

🇨🇭 Switzerland

Primary endpoints

Insulin sensitivity; Ectopic lipids; Oxidative capacity

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov