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Clinical Trials/NCT02533024
NCT02533024CompletedNot Applicable

Preoperative Prevalence of Ulnar Neuropathy and Changes in Ulnar Nerve Latency During Surgery

University of Toledo Health Science Campus1 site in 1 country4 target enrollmentStarted: August 1, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
4
Locations
1
Primary Endpoint
Prevalence of ulnar neuropathy in patients scheduled to undergo anesthesia and surgery as measured by electromyography

Study Overview

Brief Summary

This study is to investigate the incidence of undiagnosed ulnar neuropathy in patients undergoing surgery. The investigators hope to determine if patients with ulnar neuropathy have changes in nerve conduction latency during surgery.

Detailed Description

After obtaining an informed consent, the participating subjects will be asked a few questions relating to ulnar nerve dysfunction. Following this the investigators will do a focused physical exam looking for decrement of sensation in the distribution of the ulnar nerve and muscle strength of the hand muscles supplied by the ulnar nerve. After this the subjects will undergo an EMG exam to measure the conduction velocity of the ulnar nerve. Basically the nerve will be stimulated with a small current and the resultant muscle activity of the hand muscle will be picked up using an EKG like patch applied to the skin over the hand. If a subject is diagnosed to have ulnar neuropathy preoperatively the investigators would study the EMG based nerve conduction during surgery at 30-60 minute intervals for the duration of surgery. For purposes of comparison the investigators would measure the ulnar nerve conduction during surgery in age and sex matched controls.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
50 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •50 yrs of age or older
  • •Scheduled to undergo a surgical procedure at UTMC with an anticipated length of 2hours or greater

Exclusion Criteria

  • •Less than 50yrs
  • •Not scheduled for a surgical procedure at UTMC or scheduled for a surgical procedure with an anticipated length of less than 2hours

Arms & Interventions

Group Cohort

Experimental

All subjects will have nerve conduction studies (Electromyography/EMG) pre-operatively, monitored intra-operatively and immediately post-operative.

Intervention: Electromyography (Other)

Outcomes

Primary Outcomes

Prevalence of ulnar neuropathy in patients scheduled to undergo anesthesia and surgery as measured by electromyography

Time Frame: Day 1

Prevalence of undiagnosed or subclinical ulnar neuropathy as determined by electromyography

Secondary Outcomes

  • Latency (ms)(Day 1)
  • Amplitude (mV)(Day 1)
  • Velocity (m/s)(Day 1)

Investigators

Sponsor
University of Toledo Health Science Campus
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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