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:
2025-12-24 @ 9:46 PM
Ignite Modification Date:
2025-12-24 @ 9:46 PM
NCT ID:
NCT04683432
Eligibility Criteria:
Inclusion Criteria:
* Male
* Chinese ethnicity
* Age between 21-40 years
* Weigh at least 45 kg
* Body mass index between 18to 25 kg/m²
* Normal blood pressure (\</=140/90 mmHg)
* Fasting blood glucose \<6.0 mmol/L
* Healthy dentition and ability to bite, chew and swallow normally
* No history of pain or discomfort in jaw movements or excessive teeth clenching or grinding, no caries or periodontal disease and no impaired salivation functions
Exclusion Criteria:
* Partake in sports at the competitive and/or endurance levels
* Have known glucose-6-phosphate dehydrogenase (G6PD) deficiency
* Have known history of anaemia or thalassemia minor
* Have major chronic disease such as heart disease, cancer or diabetes mellitus
* Take insulin or drugs known to affect glucose metabolism
* Intentionally restrict food intake
* Have major medical or surgical event requiring hospitalization within the preceding 3 months
* Have taken antibiotics for 3 months before the study period
* Smoker
* Overnight shift worker
* Have any known food allergy (eg. anaphylaxis to peanuts)
* Have an active Tuberculosis (TB) condition 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)
* Member of the research team or their immediate family members. Immediate family member is defined as a 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
* Have poor veins impeding venous access
* Have any history of severe vasovagal syncope (blackouts or near faints) following blood draws
Healthy Volunteers:
True
Sex:
MALE
Minimum Age:
21 Years
Maximum Age:
40 Years
Study:
NCT04683432
Study Brief:
Protocol Section:
NCT04683432