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Comparison of the Efficacy of the Ultrasound With Fluoroscopy in Guidance of Lumbar Sympathetic Block: A Prospective Randomized Open-label Trial
This study compares the efficacy of the ultrasound with fluoroscope in guidance of lumbar sympathetic block (LSB). The goals of the study are; 1) To show that US-guided LSB results in shorter performance time compared to fluoroscope-guided LSB, 2) To evaluate the efficacy and safety of US-guided LSB, and 3) To verify that US-guided LSB has similar success rates to fluoroscope-guided LSB. 50 patients who are supposed to undergo LSB due to sympathetically maintained pain, satisfy criteria of inclusion and exclusion, and voluntarily sign the informed consent will be enrolled.
Age
18 - 85 years
Sex
ALL
Healthy Volunteers
No
Seoul National University Hospital
Seoul, South Korea
Start Date
April 1, 2016
Primary Completion Date
November 1, 2017
Completion Date
November 1, 2017
Last Updated
June 10, 2016
50
ESTIMATED participants
24G intravenous route for Lumbar Sympathetic Block (LSB):
PROCEDURE
15-cm Chiba needle for Lumbar Sympathetic Block (LSB)
DEVICE
Ultrasound for Lumbar Sympathetic Block (LSB)
DEVICE
Fluoroscope for Lumbar Sympathetic Block (LSB)
DEVICE
10 ml of 0.25% levobupivacaine injection for LSB
DRUG
Temperature measurement for Lumbar Sympathetic Block (LSB)
PROCEDURE
Postprocedure care for LSB
PROCEDURE
Lead Sponsor
Seoul National University
NCT07473635
NCT05777889
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05052736