MedTrace Logo

Continuous Blockade of the Brachial Plexus

NCT02769429 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 53

Last updated 2019-07-25

No results posted yet for this study

Summary

This study will answer the question whether there is a difference in the effects and complication rates of ultrasound guided continuous interscalene block (CISB) and nerve stimulation-guided continuous cervical paravertebral block (CCPVB). The aim of this study is to evaluate the differences in efficacy and side effects - if any.

Conditions

Interventions

DEVICE

Ultrasound-guided CISB

This group will receive ultrasound-guided CISB with the catheter placed on the upper trunk of the brachial plexus

DEVICE

nerve stimulator-guided CCPVB

This group will receive landmark with nerve stimulator based needle placement and then nerve stimulator-guided CCPVB with the catheter placed on the 6th cervical spinal root

Sponsors & Collaborators

  • I. Heermann Anesthesia Foundation

    collaborator UNKNOWN

  • University of Florida

    lead OTHER

Principal Investigators

  • Yury Zasimovich · University of Florida

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-09-19
Primary Completion
2018-06-06
Completion
2018-09-26

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02769429 on ClinicalTrials.gov