About this trial
This is a human clinical study making a noninvasive measurement from a patient's eye to determine whether there is a quantitative difference in measurements between patients with and without the diagnosis of dementia.
Eligibility criteria
Qualifiers
All patients must be capable of an adequate ophthalmic evaluation and testing. This includes the ability to cooperate with the exam, sufficiently clear media (cornea, lens, vitreous) and sufficient pupillary dilation.
Patients must be capable of providing informed consent.
Patients who are not medically stable or who may be at significant risk to their health will not be eligible.
Women of child bearing age must not be pregnant at the time of examination.
Disqualifiers
None
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
MD Stem Cells
Lead sponsor
Jeffrey N Weiss MD
Collaborator
3T Radiology
Collaborator
The Healing Institute
Collaborator