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Use of Galvanic Skin Response to Measure Peripheral Block Activity

NCT05678777 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2023-01-10

No results posted yet for this study

Summary

the investigators aim in this study is to determine whether the block is successful in successful infraclavicular brachial plexus blocks performed with USG, according to the change in GSR value in the upper extremity blocked due to sympathetic nerve blockade. Block success will be evaluated by sensory and motor examination of the blocked arm.

Conditions

  • Regional Anesthesia

Interventions

DEVICE

Galvanic Skin Response

The probe will be attached to the patient's finger and the Galvanic Skin Response will be measured

Sponsors & Collaborators

  • Adiyaman University

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-01-30
Primary Completion
2023-02-28
Completion
2023-03-30

Countries

  • Turkey (Türkiye)

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 NCT05678777 on ClinicalTrials.gov