Clinical Trial Details
— Status: Completed
Administrative data
| NCT number |
NCT02532582 |
| Other study ID # |
STU00105002 |
| Secondary ID |
|
| Status |
Completed |
| Phase |
|
| First received |
|
| Last updated |
|
| Start date |
May 2015 |
| Est. completion date |
May 2020 |
Study information
| Verified date |
April 2021 |
| Source |
Northwestern University |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Observational
|
Clinical Trial Summary
The purpose of this study is to ultimately prevent injuries to nerves during surgical
procedures. Living donor liver transplant or hepatectomy (removal of a piece of the liver)
patients will receive an arterial line as standard of care. The arterial line helps monitor
blood pressure along with the compression of important vessels during surgery. In addition,
research participants will undergo neuromuscular monitoring using Somato-Sensory Evoked
Potential (SSEP) or Evoked Potential Assessment Device (EPAD). During an operation,
neuromuscular monitoring can tell doctors if the nerves being studied are working normally or
if they are at risk for injury. This study will help investigators to understand what kind of
monitoring is best to prevent nerve injuries during a surgical procedure.
Description:
As standard of care, research participants undergoing a living donor liver transplant or
other liver surgeries will receive a right-sided radial arterial line to monitor his/her
blood pressure along with the compression of important vessels during surgery. These
measurements will be captured throughout the surgical procedure. If blunting of the arterial
line wave form occurs, the anesthesiology team alerts the surgical team to release the
retractors until the wave form returns to baseline. Depression of the radial arterial line
wave form will be captured, time-stamped, and stored by the research transplant
anesthesiology team.
Additionally as part of research, participants will receive neuromuscular monitoring using
SSEP or EPAD to measure their nerve signals during the surgery (3-6 hours). SSEP or EPAD
measurements will occur at the median and ulnar nerve and will be captured throughout the
surgical procedure. The research neuromonitoring team will consists of highly skilled
technicians, who monitor patients during neurosurgical and orthopedic surgeries. SSEP or EPAD
output captured during the surgery will be time-stamped, stored, and interpreted by a
Neurologist. To investigate if a correlation exists, SSEP or EPAD abnormalities will be
correlated and analyzed with the arterial wave form depressions.
To determine whether a correlation exists with clinical outcomes, a prospective medical
record review will be conducted. Before performing the prospective medical record review,
authorized research personnel will obtain informed consent from each participant.