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Clinical Efficacy of Axillary Block in Cervical Radiculopathy

NCT05723354 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2023-02-15

No results posted yet for this study

Summary

The primary endpoint of this study was to compare the clinical efficacy of axillary block in patients of cervical radiculopathy using 2 volumes of local anesthetics.

Conditions

  • Pain, Chronic

Interventions

PROCEDURE

axillary block guided by ultrasound

axillary block using local anesthetics

Sponsors & Collaborators

  • Keimyung University Dongsan Medical Center

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2023-02-13
Primary Completion
2023-11-30
Completion
2023-11-30

Countries

  • South Korea

Study Locations

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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 NCT05723354 on ClinicalTrials.gov