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Superficial Cervical Plexus Block for IJCL Pain Management

NCT05252832 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 14

Last updated 2025-05-04

No results posted yet for this study

Summary

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

Conditions

  • Superficial Cervical Plexus Block
  • Pain

Interventions

PROCEDURE

Superficial Cervical Plexus Block

Location of injection for block.

PROCEDURE

Local Infiltrate

Local infiltration location.

Sponsors & Collaborators

  • Cleveland Clinic Akron General

    lead OTHER

Principal Investigators

  • Robert Stenberg, MD · Cleveland Clinic Akron General

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-01-15
Primary Completion
2024-01-20
Completion
2024-12-31

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 NCT05252832 on ClinicalTrials.gov