Visual Evoked Potential Reliability during Non-Cranial Surgery

Overview

About this study

The goal of this study is to determine the optimal stimulating and recording protocol for visual evoked potentials (VEP’s) during non-cranial surgery using total intravenous anesthesia (TIVA). The study will also determine if VEP’s remain reliably stable in amplitude and latency during non-cranial surgery using total intravenous anesthesia (TIVA), and also determine what factors predict poorly reliable VEP’s during non-cranial surgery using TIVA.

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:

Non-cranial surgical patients with other evoked potentials being monitored
TIVA used during surgery

Exclusion Criteria:

Ppatients blind in both eyes

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 Ruple Laughlin, M.D.	Closed for enrollment

Mayo Clinic Location

Status

Rochester, Minn.

Mayo Clinic principal investigator

Ruple Laughlin, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Clinical Trials