CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 40 enrolled
Drug / intervention
SSEP monitoringdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03409536
NCT03409536N/ACompleted
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Evaluation of the Diagnostic Threshold of SSEP of Brachial Plexus Injury

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's·observational·Posted Jan 24, 2018·Updated Feb 19, 2020

In Brief

An observational study evaluating SSEP monitoring for Brachial Plexus Injury and Peripheral Nerve Injuries. Completed, enrolled 40 participants across 1 site.

Detailed Summary

Brachial plexus block is a common regional anesthesia technique which is performed by anesthesiologists to anesthetize the arm for surgery. In this study, we are investigating the relationship between the nerve conduction (induced by brachial plexus block) and the patients' symptoms before and after the brachial plexus block. We will attach a nerve conduction device (SSEP device) to monitor the patients' arm conduction and we will assess the patients' symptoms simultaneously.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsBrachial Plexus Injury, Peripheral Nerve Injuries
CountriesCanada
Collaborators--

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedJan 24, 2018
Enrollment StartJan 1, 2018
Primary CompletionDec 31, 2019
TodayJul 2, 2026
Enrollment to primary: 2 yearsPosted 8.4 years ago

Interventions

SSEP monitoringdevice

Participants will be monitored using the SSEP device both before and after induction of a brachial plexus block.