Comparison of Standard Visually Evoked Potential (VEP) Recording and a Portable VEP System
Overview
Tab Title Description
Study type
ObservationalDescribes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
Study IDs
Site IRB
- Scottsdale/Phoenix, Arizona: 15-009668
Sponsor Protocol Number: 15-009668
About this study
Visually Evoked Potentials (VEPs) are electrical potentials elicited from brief visual stimuli and recorded from the visual cortex with surface electrodes. VEPs are an objective, reliable, and non-invasive method for evaluation of the functional integrity of the retina and early afferent visual pathways. The purpose of this study is to compare the VEPs generated from a standard clinical evoked potential system to those obtained from the Vivonics portable VEP system.
Participation eligibility
Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.
Inclusion Criteria:
-
Concussion Group
- ≥13 years, and able to provide informed consent
- Under evaluation or management of suspected concussion / TBI
- No alcohol within 48 hours of testing
- Corrected visual acuity of 0.00 logMAR (20/20) confirmed with Snellen chart
-
Control Group
- ≥13 years, and able to provide informed consent
- No acute concussion / TBI history
- No alcohol within 48 hours of testing
- Corrected visual acuity of 0.00 logMAR (20/20) confirmed with Snellen chart
Exclusion Criteria:
- Inability to tolerate the visual stimulus
- History of seizures, stroke
- Strabismus, amblyopia
- History of degenerative neurological condition
Participating Mayo Clinic locations
Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.
| Mayo Clinic Location |
Status |
|
Scottsdale/Phoenix, Ariz.
Mayo Clinic principal investigator Jamie Bogle, Au.D., Ph.D. |
Closed for enrollment |
|
More information
Publications
Publications are currently not available