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Clinical Trial Summary

This is a prospective randomized trial evaluating the effect of SCPB on reported patient pain following IJCL placement as compared to local infiltrate.


Clinical Trial Description

The goal of this study is to determine if SCPBs provide more pain control than local infiltrate of anesthetic for internal jugular venous cannulation. The investigators hypothesis that patients who receive the SCPB will have a lower VAS rating on average than those who receive local infiltration following internal jugular venous cannulation. To test this, the investigators will be approaching eligible patients for inclusion in a research study. If the patients consent, the patients will be randomly assigned the standard of care treatment or the SCPB. The investigators will then ask the patients to rate pain following insertion of the central line. The investigators will also evaluate different aspects of the patient's hospital course to evaluate their outcomes. ;


Study Design


Related Conditions & MeSH terms

  • Pain
  • Superficial Cervical Plexus Block

NCT number NCT05252832
Study type Interventional
Source Cleveland Clinic Akron General
Contact Robert Stenberg, MD
Phone 330-344-6306
Email stenber@ccf.org
Status Recruiting
Phase N/A
Start date January 15, 2022
Completion date December 31, 2024

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