Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Qualissima
With
European Union
Age
50–90
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
PART A:
1. Written Informed Consent to participate in a up to 3 year imaging study
2. Male and female aged between 55-90 years
3. Memory complaint by patient or partner that is verified by a physician. (Memory complains expressed by the patients or their informant that the examiner considers to be relevant and exceed those expected for a patient of their age. The patient may or may not have symptoms of deficiency in other cognitive areas.)
4. Abnormal memory functions documented by scoring 1 SD below the age-adjusted mean on the Logical Memory II subscale, (Delayed Paragraph Recall) from the Wechsler Memory Scale.
5. General cognition and functional performance sufficiently preserved such that a diagnosis of Alzheimer's disease cannot be made by the site physician at the time of the screening visit.
6. Mini-Mental State Exam score between 24 and 30 (inclusive)
7. Clinical Dementia Rating = 0.5. Memory Box score must be at least 0.5.
8. Amnestic Mild Cognitive Impairment (MCI) (pure amnestic or multidomain)
9. Geriatric Depression Scale less than 6
10. Hachinski Modified Ischemic scale\< to 4
11. Patient is untreated or under a permitted medication (Cholinesterase inhibitors and memantine, before the enrolment and newly prescriptions during the study, are permitted for aMCI patients.)
12. At least 5 grades education
13. Must speak (language) fluently
14. Have a study partner with 10+ hr/wk contact (can be in person and telephone), accompanies to visits
15. Willing and able to comply with the requirements of the study, as judged by the investigator
You may not be if
PART B:
PART A:
1. Ischaemic lesions already detected in a previous scan
2. Head injury with loss of consciousness \> 24 hours
3. Current substance abuse
4. Current therapy with steroids or current chemotherapy
5. Loss of weight \> 5 kg in the last 6 months
6. Systemic disease with frequent involvement of the CNS (lupus, HIV, rheumatoid arthritis)
7. CNS disease diagnosed by a specialist or in treatment (such as epilepsy, ictus)
8. Cerebral metastasis or CNS primary tumour still benign (except for pituitary microadenoma)
9. Suspected multiple sclerosis + MRI evidence of white matter lesions
10. Suspected recent stroke + MRI evidence of infarct
11. Aneurysm \> 10 mm and arteriovenous malformations (except for venous angioma)
12. Dysgenesia of central nervous system
PART B:
1. Visual and auditory acuity inadequate for neuropsychological testing
2. Enrolment in other trials or studies not compatible with study objectives (in particular, those with experimental drugs)
3. History of significant neurological or psychiatric illnesses or presence of other diseases precluding enrolment.
4. Use of forbidden medications
6. Excluded Medication: Antidepressants with anti-cholinergic properties and within 4 weeks of the screening: Regular use of narcotic analgesics (\>2 doses per week), Use of neuroleptics with anti-cholinergic properties (e.g., chlorpromazine, thioridazine), Chronic use of other medications with significant central nervous system anticholinergic activity (e.g., diphenhydramine), Use of Anti-Parkinsonian medications (including Sinemet, amantadine, bromocriptine, pergolide, selegiline), Participation in any other investigational drug study (individuals may not participate in any drug study while participating in this protocol). Diuretic drugs should not be started or discontinued within 4 weeks prior to screening (Any change in diuretic medication during the study should be reported).
