A Study to Compare Bifrontal Montage Agreement
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
- Rochester, Minnesota: 19-000568
NCT ID: NCT04062240
Sponsor Protocol Number: 19-000568
About this study
The purpose of this study is to determine measurement difference and variability of bispectral index (BIS) values when monitored in a bilateral frontal montage.
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:
- Adult patient having elective cardiac surgery.
Exclusion Criteria:
- Patient refusal.
- Pediatric patients.
- Emergency procedure.
- Patients with known or suspected carotid or erebrovascular disease.
- Patients with prior stroke.
- Skin condition or anatomy preventing proper sensor placement.
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 |
|
Rochester, Minn.
Mayo Clinic principal investigator Wade Kreun, R.N. |
Closed for enrollment |
|
More information
Publications
Publications are currently not available