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 @ 12:00 AM
Ignite Modification Date:
2025-12-25 @ 12:00 AM
NCT ID:
NCT01238458
Eligibility Criteria:
Inclusion Criteria:
* Both genders ≥ 50 years old.
* Written and dated informed consent by self or by legal representative, to be obtained before any of the study procedures.
* 30 cognitively normal volunteers with no evidence of significant cognitive impairment by history and psychometrictesting (MMSE \> 24).
* 60 subjects with a diagnosis of AD according to the NINCDS-ADRDA criteria.
* 60 subjects with a diagnosis of MCI
Exclusion Criteria:
1. Pregnant or becoming pregnant during the study (as documented by pregnancy testing at screening or at any date during the study according to the PI discretion) or current breast feeding.
2. Modified Hachinski ischemic score of \>4 or those who meet the NINDS-AIREN criteria for vascular dementia.
3. Any subject who has a clinically significant abnormal laboratory values, and/or clinically significant or unstable medical or psychiatric illness.
* Clinically significant hepatic, renal, pulmonary, metabolic, or endocrine disturbances, especially thyroid disease;
* Current clinically significant cardiovascular disease. Clinically significant cardiovascular disease usually includes one or more of the following:
* cardiac surgery or myocardial infarction within the last 6 months;
* unstable angina
* coronary artery disease that required a change in medication within the last 3 months
* decompensated congestive heart failure
* significant cardiac arrhythmia or conduction disturbance, particularly those resulting in atrial or ventricular fibrillation, or causing syncope, near syncope, or other alterations in mental status
* severe mitral or aortic valvular disease
* uncontrolled high blood pressure
* congenital heart disease
* clinically significant abnormal result on ECG, including but not limited to QTc\>450 msec iii. Clinically significant infectious disease, including AIDS or HIV infection or active hepatitis B, active hepatitis C, HIV-1, or HIV-2
4. History of drug or alcohol abuse within the last year, or prior prolonged history of abuse.
5. Patients who have the evidence of neurodegenerative disorders other than AD, cognitive impairment resulting from trauma or brain damage, brain infarction, clinically significant psychiatric disease, epilepsy, are excluded.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
50 Years
Study:
NCT01238458
Study Brief:
Protocol Section:
NCT01238458