Obesity Trial, Recruiting
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:
- Healthy men and women who are using contraception during the study and for 3 months after it ends
- People aged between 18 and 65 years old at the time of signing the consent form
- People with a body mass index (BMI) either between 18.5 and 25, or between 30 and 35 (confirm with trial site which range applies)
- People who are willing and able to take part in the full study, including drinking a special sugar drink containing a tracer substance called 14C-glucose and eating the meals provided
- People who have regular bowel movements, meaning they typically have between 1 and 3 stools per day
- People who normally eat three meals a day — breakfast, lunch, and dinner
Who may not be able to join:
- People who have been diagnosed with any type of diabetes (Type 1, Type 2, or a genetic form)
- People who have been diagnosed with heart disease or high blood pressure (readings of 140 mmHg or higher on the top number, and/or 90 mmHg or higher on the bottom number)
- People with a blood sugar control reading (HbA1c) higher than 53 mmol/mol
- People with a significant history of heart, kidney, liver, breathing, gut, immune system, hormonal, nerve, or mental health conditions
- People who have been diagnosed with a breathing condition such as COPD or asthma
- People with a history of movement disorders or problems with muscle or fat metabolism
- People with known severe kidney problems
- People with a stomach or gut ulcer, or a strong history of indigestion
- People with a recent or ongoing history of diarrhoea
- People with known anaemia (low iron or low red blood cells)
- People with a personal or family history of blood clots, epilepsy, seizures, or schizophrenia
- People who regularly use dietary supplements more than 3 times per week
- People who regularly take any prescribed or over-the-counter medications (except contraceptives or contraceptive devices)
- People with a history of drug or alcohol misuse in the past two years
- People who test positive for alcohol at the screening or admission appointment
- People who use recreational drugs
- People who experience claustrophobia (fear of enclosed spaces)
- People who are currently following a weight-loss diet or a high-calorie or high-protein diet aimed at gaining weight
- People with ongoing constipation
- People with known allergies or intolerances to any of the 14 major food allergens — celery, gluten-containing grains, crustaceans, eggs, fish, lupin, milk, molluscs, mustard, tree nuts, peanuts, sesame seeds, soybeans, or sulphur dioxide/sulphites — or a history of conditions affecting nutrient absorption, including coeliac disease
- People who regularly experience gut problems such as abdominal pain, stomach upsets, or loud bowel sounds, or who have known or suspected irritable bowel syndrome
- People who are currently taking part in another research study
- People who have received a product containing the tracer substance 14C in the past 12 months
- People who are pregnant or breastfeeding
- People who currently smoke or who have used nicotine-containing products in the 6 months before the study
- People who have taken antibiotics in the 60 days before the study's preparation period begins
- People who are currently following a structured, progressive resistance training programme more than 3 times per week
- People assessed as having a sedentary (very inactive) lifestyle based on the International Physical Activity Questionnaire (IPAQ)
- People who are unable to give informed consent
- People who are employed by, or completing a thesis or internship at, the department of Human and Animal Physiology linked to this trial
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.
Contact this trial
Principal Investigator: Marlou Dirks, PhD, Wageningen University
Phone: +31 317-484 136
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
Where this trial is recruiting
Primary endpoints
Total mass balance (cumulative recovery of 14C)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.