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NOT YET RECRUITING
NCT06130514
NA

The Comparison of Sympathetic Blockade of Stellate Ganglion Block and Thoracic Sympathetic Ganglion Block

Sponsor: Seoul National University

View on ClinicalTrials.gov

Summary

For patients scheduled to undergo upper limb sympathetic nerve block due to chronic neuropathic pain in the upper limb lasting more than 3 months, the ultrasound-guided stellate ganglion block group (S group) and the fluoroscopy-guided thoracic sympathetic nerve block group (T) Patients are randomly assigned 1:1 to one of the groups, and the procedure is performed. To evaluate the effectiveness of sympathetic nerve blockade, temperature changes in both palms are measured twice, 20 minutes before and 20 minutes after the procedure, using an infrared thermographer. Other variables related to the procedure are surveyed by outpatient visit or telephone before the procedure, after the procedure, before returning home, and 1 week and 1 month after the procedure.

Official title: The Comparison of Sympathetic Blockade of Stellate Ganglion Block and Thoracic Sympathetic Ganglion Block in Patients With Chronic Upper Extremity Neuropathic Pain: a Prospective Randomized and Comparative Clinical Trial

Key Details

Gender

All

Age Range

19 Years - 85 Years

Study Type

INTERVENTIONAL

Enrollment

118

Start Date

2024-07-10

Completion Date

2026-01-10

Last Updated

2024-05-29

Healthy Volunteers

No

Interventions

DEVICE

Ultrasound

Ultrasound-guided stellate ganglion block with 1% mepivacaine 5 mL

DEVICE

Fluoroscopy

Fluoroscopic-guided thoracic sympathetic ganglion block with 1% mepivacaine 3 mL