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 @ 7:52 PM
Ignite Modification Date: 2025-12-24 @ 7:52 PM
NCT ID: NCT05050604
Eligibility Criteria: Inclusion Criteria: * Age ≥ 50 years * Patients with vascular cognitive impairment according to modified Fazekas scale grade 2\~3 and/or more than 3 of lacunar infarction in Supratentorial * Patients with Clinical Deterioration Rating(CDR) score of 0.5 * Patients with Korean-Montreal Cognitive Assessment (K-MoCA) score of 23 or less * Walk or move using walking aids (i.e., walkers, walking sticks or wheelchairs) * Written informed consent Exclusion Criteria: * Clinical diagnosis of dementia (including secondary dementia due to Alzheimer's disease, vascular dementia, infections of the central nervous system (e.g., HIV, syphilis), Creutzfeld-Jacob disease, Pixie disease, Huntington's disease, Parkinson's disease, etc.) * Medication of dementia within the past 3 months. (e.g., donepezil, galantamine, rivastigmine, memantine) * Medication of brain functional improvement medication within the past 6 weeks. (e.g., citicoline, oxiracetam, piracetam, choline alfoscerate, Nicergoline, Nimodipine, ginko-biloba, acetyl-l carnitine) * No studies (no regular school entrance), illiteracy * Stroke within the past 3 months * Abnormal results from Vitamin B12, Thyroid Stimulated Hormone Test (TSH), HIV-Ab, and VDRL test contribute to or contribute to cognitive impairment of the subject * Serious mental disorders such as severe depression, schizophrenia, alcoholism, drug dependence, etc. * Severe cardiovascular disease such as myocardial infarction, unstable angina or heart failure within the past 6 months
Healthy Volunteers: False
Sex: ALL
Minimum Age: 50 Years
Study: NCT05050604
Study Brief:
Protocol Section: NCT05050604