Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:03 AM
Ignite Modification Date:
2025-12-25 @ 4:03 AM
NCT ID:
NCT06554002
Eligibility Criteria:
Inclusion Criteria:
* 21 to 60 years old
* Group A: 21 - 25 kg/m2, with first degree family history of type 2 diabetes, or Group B: 23 - 30 kg/m2, with waist circumference \>85 cm for males and \>82 cm for females
Exclusion Criteria:
* • Consume fibre supplements or any other supplements that is likely to interfere with study outcomes
* Have any major organ dysfunction (e.g. cardiovascular, respiratory, hepatic, renal, gastrointestinal) that may influence taste, olfaction, appetite, digestion, metabolism, absorption or elimination of test foods, nutraceutical or drug
* Smoking
* Have any metabolic diseases (e.g. diabetes, hypertension)
* Have medical conditions and/or taking medications known to affect glycaemia (e.g. glucocorticoids, thyroid hormones, thiazide diuretics)
* Have glucose-6-phosphate dehydrogenase (G6PD) deficiency
* Have any severe food allergy (e.g. anaphylaxis to peanuts), or any other known food allergy/intolerance
* Have active Tuberculosis (TB) or currently receiving treatment for TB
* Have any known Chronic infection or known to suffer from or have previously suffered from or is a carrier of Hepatitis B Virus (HBV), Hepatitis C Virus (HCV), Human Immunodeficiency Virus (HIV)
* A team member of the study or their immediate family members (i.e. spouse, parent, child, or sibling, whether biological or legally adopted)
* Enrolled in a concurrent research study judged not to be scientifically or medically compatible with the study of the CNRC.
* Intentionally restricting food intake
* Have poor veins impeding venous access
* Have any history of severe vasovagal syncope (blackouts or near faints) following blood draws
* Have claustrophobia
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
21 Years
Maximum Age:
60 Years
Study:
NCT06554002
Study Brief:
Protocol Section:
NCT06554002