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:
2025-12-26 @ 1:17 PM
Ignite Modification Date:
2025-12-26 @ 1:17 PM
NCT ID:
NCT01746706
Eligibility Criteria:
Inclusion Criteria:
patients:
* \- A score in the MMS (Folstein and al ., on 1975, French version subjected to consensus of Greco). 24 for the level subjects I (less than 5 years of study), 26 and more for the others, the autonomy in the everyday life,
* A lower normal IADL \< = 1/4 (Lawton and Brody, on 1969, version 4 items),
* A complaint mnemonic of the patient
* A lower performance of 1,5 standard deviation in the standard in the reminder(abseiling) postponed from the sub-test of logical memory(report) of the WMS-III and/or in the free reminder(abseiling) postponed from the test(event) of the California Verbal Learning Test.
volunteers:
* 50-80-year-old and presented an educational level sailed in that of the patients,
* a MMS upper to 24 for the level subjects I (5 years of study), 26 and more for the levels 2 and 3,
* an Autonomy of the everyday life,
* normal IADL = 0/4
* did not present mnemonic complaint,
* a performance normal for the reminder postponed from the subtest of logical memory of the WMS-III and for the free reminder(abseiling) postponed from the test(event) of the California Verbal Learning Test.
Exclusion Criteria:
* Incapacitated to realize the examination by FART because of medical intercurrent affections. There are this day no contraindications in the product Florbetapir used for the TEPscan.
* The persons under protection of justice cannot be included, because the law forbids their participation biomedical researches.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
50 Years
Maximum Age:
90 Years
Study:
NCT01746706
Study Brief:
Protocol Section:
NCT01746706