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Prediction of Clinical Outcome in Axillary Block

NCT05723419 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 70

Last updated 2023-02-15

No results posted yet for this study

Summary

The primary endpoint of this study was to identify that Perfusion index (PI) has any predictive value for the treatment outcome of cervical radiculopathy

Conditions

  • Pain, Chronic

Interventions

PROCEDURE

axillary block using 5 ml local anesthetics

ultrasoud guided axillary block

Sponsors & Collaborators

  • Keimyung University Dongsan Medical Center

    lead OTHER

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 NCT05723419 on ClinicalTrials.gov