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

CompletedNot applicableNCT04876989
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The purpose of this study is to investigate the effect of ultrasound-guided thoracic paravertebral block (TPVB) when performing sympathetic block for upper limb pain control.

Study details

Official title
The Comparison of Sympathetic Blockade of Stellate Ganglion Block and Thoracic Paravertebral Block in Patients With Chronic Upper Extremity Neuropathic Pain: a Prospective Randomized and Comparative Clinical Trial
Conditions
Interventions
  • Procedure: US-SGB
  • Procedure: US-TPVB
Sponsor
Seoul National University
Collaborators
SMG-SNU Boramae Medical Center
Start date
2021-07-21
Primary completion
2022-12-19
Sex
All
Age range
from 19 Years to 85 Years
Results posted
No results posted in this snapshot
Countries
South Korea
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Clinical diagnosis of complex regional pain syndrome * Clinical diagnosis of postherpetic neuralgia * Clinical diagnosis of phantom limb pain * Clinical diagnosis of chronic post-surgical pain * Clinical diagnosis of post-traumatic pain syndrome * Upper extremity pain lasting more than 3 months Patients with a new or known diagnosis of chronic neuropathic pain lasting more than 3 months in the upper extremity Exclusion Criteria: * Refusal of a patient * Any vascular disease in the upper extremities * Previous history of thoracic sympathetic or stellate ganglion neurolysis (e.g. -thermocoagulation, radiofrequency neuromodulation, and/or chemical neurolysis) * Coagulopathy * Systemic infection or local infection at the needle injection site * Major deformation at the level of the neck (radiotherapy, surgery, etc.) * Known allergy to local anesthetics of amide type * Inability to understand a numeric rating pain scale (cognitive dysfunction) * Patients whose palm temperature on the ipsilateral side is ≥ 36.5℃ in the thermography before the procedure

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT04876989