Nerve Stimulator for Patients With Upper Extremity Disease Vascular or Orthopedic Surgery

  • STATUS
    Recruiting
  • days left to enroll
    59
  • participants needed
    100
  • sponsor
    Rutgers, The State University of New Jersey
Updated on 22 January 2021

Summary

To help determine if there is improved pain relief when a device that makes an arm muscle move (nerve stimulator) is used to place a needle in the area above the collarbone to prevent feeling of pain (anesthesia) of the upper arm.

Description

The Investigators will use the assessment of onset of motor and sensory block Q 5 minutes to distinguish the difference between blocks performed with ultrasound guidance with or without a nerve blockade monitor.

Details
Condition Other Biomechanical Lesions of Upper Extremity
Treatment Local anesthetic block [0.35% marcaine], Braun DIG-R-C Stimuplex Blockade Monitor System
Clinical Study IdentifierNCT03112642
SponsorRutgers, The State University of New Jersey
Last Modified on22 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Adult male and females 21 through 89
Agree to study participation and signed the informed consent
Scheduled for upper extremity surgery with ultrasound guided supraclavicular block -

Exclusion Criteria

Children
Pregnant Women
Persons with allergies to local anesthetics
Persons with infections at or near site of needle insertion
Patients with severe disturbance of cardiac rhythm and heart block
Patients with severe respiratory compromise
Patients requiring bilateral upper extremity anesthesia
Patients with coagulopathy or medical anticoagulation
Patients with traumatic nerve injury to neck or upper extremity
Patients with preexisting neurological deficits in the distribution of the block
Patients with previous surgery to the neck that may distort brachial plexus anatomy
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