Eligibility Module

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 @ 9:20 PM
Ignite Modification Date: 2025-12-24 @ 9:20 PM
NCT ID: NCT03641404
Eligibility Criteria: Inclusion Criteria: * Elderly individuals 60 - 90 years of age * Chinese ethnicity (from other local cohort studies) * Demonstrate amnestic mild cognitive impairment (assessed by panel of psychiatrists) * Independent and able to travel to study site without assistance * No other severe underlying conditions or terminal illnesses * Capable of understanding the study and requirements and able to provide informed consent to participate * Willing to commit to the year-long study, comply with study administration and periodic blood and urine sampling Exclusion Criteria: * Inability to understand the risks and requirements of the study for any reason * Any intolerance to lactose, and/or allergies to mushrooms * History of cardiovascular complications, diabetes, hypertension or hypercholesterolemia, or other pre-existing condition that may prevent them from completing the study * Evidence of anaemia or other significant haematological conditions * History or mental illness, depression or other underlying psychiatric illnesses * History of drug or alcohol abuse * Involvement in another study requiring administration of an investigational compound in the past 30 days * Subjects whose blood analysis reveal and extremes of liver or kidney function markers (from baseline screening) * Deemed unfit for any reason as determined by the principal/co-investigator
Healthy Volunteers: True
Sex: ALL
Minimum Age: 60 Years
Maximum Age: 90 Years
Study: NCT03641404
Study Brief:
Protocol Section: NCT03641404