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ENROLLING BY INVITATION
NCT05544721
PHASE4
A Study of Paravertebral Block in Thoracic Outlet Syndrome
Sponsor: Mayo Clinic
View on ClinicalTrials.gov
Summary
This research is being done to evaluate the effects of receiving only a paravertebral block prior to first rib resection procedure versus receiving the block both pre and post procedure.
Official title: Pre-Operative and Post-Operative Paravertebral Block on Patients With Thoracic Outlet Syndrome.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
50
Start Date
2022-10-05
Completion Date
2027-08
Last Updated
2025-11-14
Healthy Volunteers
No
Conditions
Interventions
DRUG
Ropivacaine
0.5% 3-4 mL per level, with levels T1 and T2 will be used as the block injectate
Locations (1)
Mayo Clinic in Florida
Jacksonville, Florida, United States