Clinical Trials Directory

Trials / Terminated

TerminatedNCT03112642

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

Does the Use of a Nerve Stimulator Improve the Outcome of Ultrasound-Guided Supraclavicular Block (Anesthesia) for Upper Extremity Surgery?

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
8 (actual)
Sponsor
Rutgers, The State University of New Jersey · Academic / Other
Sex
All
Age
21 Years – 89 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
PROCEDURELocal anesthetic block [0.35% marcaine]In the absence of paresthesia and after negative aspiration, the 40 ml of local anesthetic block \[0.35% marcaine\] will be administered.
DEVICEBraun DIG-R-C Stimuplex Blockade Monitor SystemThe blockade system will be initially set at 1 milliamp. As the proximity of the tip of the needle to the components of the brachial plexus becomes evident by ultrasound approximation and the stimulation pattern of the hand and wrist, the output of the system will be reduced to .3-.5 milliamps. With use of the Braun DIG-R-C Stimuplex Blockade Monitor System.

Timeline

Start date
2013-11-01
Primary completion
2021-03-09
Completion
2021-03-09
First posted
2017-04-13
Last updated
2024-03-05
Results posted
2024-03-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03112642. Inclusion in this directory is not an endorsement.