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 @ 11:09 PM
Ignite Modification Date:
2025-12-24 @ 11:09 PM
NCT ID:
NCT01453569
Eligibility Criteria:
Inclusion Criteria:
* At least primarily educated.
* Accord with Probable Alzheimer disease of National Institute of Neurological and Communicative Disorders and Stroke and the Alzheimer's Disease and Related Disorders Association(NINCDS-ADRDA)'s Criteria.
* 10 points ≤ Minimum Mean-Square Error(MMSE) ≤ 24 points.
* Hachinski ischemia scale \<4 points.
* Hamilton depression scale ≤10 points.
* Should have stable accompanying person, or at least contact 2 hours per day, 4 days per week with accompanying person. The accompanying person should help the patient throughout the trial.
* Signed the information consent form.
Exclusion Criteria:
* Have been in other clinical trials within 30 days before this trial' start.
* women during pregnancy or lactation.
* Dementia caused by other diseases.
* previous nervous system diseases.
* Abnormal laboratory results.
* Uncontrolled hypertension.
* Unstable or serious diseases of heart, lung, liver, kidney and blood.
* Visual or auditory handicap.
* Significant focal lesions revealed by electronic computer X-ray tomography(CT) or magnetic resonance imaging(MRI) in one year before enrollment.
* Alcohol abuse or drug abuse.
* psychotic, including patients with serious depression.
* Patients being in drug therapy of Alzheimer disease which cannot be stopped.
* In treatment of heparin, Polysaccharide sulfate, mannose ester 3 weeks before the recruitment.
* Investigator consider the patient cannot finish this trial for any reason.
* Relatives or employees of the investigators, staff of the investigate centers, contract research organization and sponsor.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
50 Years
Maximum Age:
85 Years
Study:
NCT01453569
Study Brief:
Protocol Section:
NCT01453569