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 @ 12:59 AM
Ignite Modification Date:
2025-12-25 @ 12:59 AM
NCT ID:
NCT01731093
Eligibility Criteria:
Inclusion Criteria:
* Men and women age \> 64 years.
* Not demented by Hachinski Ischemic Index (≤ 4)
* English-speaking, to ensure compliance with study visit procedures.
* Female participants must not be pregnant or of childbearing potential, i.e. either surgically sterile or postmenopausal for \> 1 year.
* Stable medical condition for three months prior to screening visit, with no clinically significant abnormalities of hepatic, renal, and hematologic function defined as follows: WBC within normal limits, platelets \> 100,000, hemoglobin ≥11 mg/dL, srum creatinine ≤ 1.8 mg/dL, AST or ALT ≤ 1.5 ULN, no clinically significant abnormalities of other laboratory studies (CBC, chemistry panel, urinalysis).
* Non-diabetic confirmed by fasting serum glucose \<126 mg/dL and on no oral hypoglycemic agents or insulin treatment.
* Stable medications for 12 weeks prior to screening visit.
* Able to ingest oral medications.
* No contraindication to baseline MRI (metallic implants, pacemakers, shrapnel…etc.).
* Physically acceptable for this study as confirmed by medical history, physical exam, neurological exam and clinical tests.
Exclusion Criteria:
* Significant neurologic disease such as Parkinson's disease, stroke, brain tumor, multiple sclerosis or seizure disorder.
* Major depression in past 12 months (DSM-IV criteria) major mental illness such as schizophrenia, or recent (in past 12 months) alcohol or substance abuse.
* History of invasive cancer within the past two years (excluding non-melanoma skin cancer).
* Contra-indications to lumbar puncture (bleeding disorder, platelet count \< 100,000, anticoagulant treatment, major structural abnormality or sepsis in the area of the lumbosacral spine, previous lower back surgery that would make LP technically difficult, hypersensitivity to lidocaine).
* Other conditions that will contribute to oxidative stress including but not limited to current smokers of cigarettes or cigars (within past month), history of alcohol or drug abuse as determined by medical history review.
* Known sensitivity, intolerance, or allergies to yeast or selenium-based compounds.
* Daily intake of more than 75 µg selenium/day (US RDA) in the 90 days prior to enrollment.
* Use of any investigational agents within 90 days prior to screening.
* Major surgery within eight weeks prior to the Baseline Visit.
* Severe unstable medical illnesses, including uncontrolled cardiac conditions or heart failure (New York Heart Association Class III or IV).
* Extremes of body weight (\<100 or \>240 lbs) to exclude upper and lower 5th percentiles for age that may influence PK and safety data.
* Residence in a skilled nursing facility.
* Blindness, deafness, language difficulties or any other disability that may prevent the subject from participating or cooperating in the protocol.
* Safety laboratory values deemed clinically significant by investigator.
Excluded Medications:
* Experimental drugs.
* Coumadin or heparin.
* Insulin or other hypoglycemic agents.
* Supplements containing more than 75 µg selenium/day (US RDA) in the 12 weeks prior to enrollment.
* The maximum dose of vitamin E (α-tocopherol) permitted in supplements will be 400 IU/day, vitamin C 1000 mg/day.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
65 Years
Study:
NCT01731093
Study Brief:
Protocol Section:
NCT01731093