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 @ 9:23 PM
Ignite Modification Date:
2025-12-24 @ 9:23 PM
NCT ID:
NCT01099332
Eligibility Criteria:
Inclusion Criteria:
* Alzheimer's disease mild to moderate as diagnosed by standard clinical, functional and NINDA-ADRDA criteria
* Mild cognitive impairment diagnosed by standard clinical, functional and NINDA-ADRDA criteria
* All subjects able to swallow Tablets
* Subjects taking copper or zinc containing supplements must have a 30-day wash out before starting study materials
* Screening laboratory values either within normal limits or deemed not clinically significant by investigator
Exclusion Criteria:
* Subjects or their study companions/care givers unable to give adequate informed consent
* Presence of a disease or condition known to affect biometal homeostasis
* Presence of psychosis, substance abuse or other major medical or neurological issues
* Presence of vascular dementia
* Clinically significant anemia at the time of the screening visit
* Current use of a decoppering drug such as trientine or penicillamine
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
55 Years
Maximum Age:
90 Years
Study:
NCT01099332
Study Brief:
Protocol Section:
NCT01099332