Pain Relief After High Thoracic Eretor Spinae Block
CompletedNot applicableNCT05487313
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 primary endpoint of this study was to identify if the ESPB in the patients of cervical radiculopathy has the effect of pain relief. The secondary endpoint of this study was to identify the spread level in the craniocaudal direction when performed at the T2 level.
Study details
- Official title
- Comparison of Pain Relief During High Thoracic Erector Spinae Plane Block Using Different Volumes of Local Anesthetics
- Conditions
- Interventions
- Sponsor
- Keimyung University Dongsan Medical Center
- Start date
- 2022-08-12
- Primary completion
- 2023-03-21
- Sex
- All
- Age range
- from 20 Years to 80 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: * cervical facet joint arthrosis * cervical foraminal stenosis * cervical herniated intervertebral disc * myofascial pain syndrome of upper back muscle Exclusion Criteria: * Allergy to local anesthetics or contrast medium * pregnancy * prior history of cervical spine surgery * coagulation abnormality
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05487313