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Pre-Operative and Post-Operative Paravertebral Block on Patients With Thoracic Outlet Syndrome.
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.
Details
| Lead sponsor | Mayo Clinic |
|---|---|
| Phase | Phase 4 |
| Status | ENROLLING_BY_INVITATION |
| Enrolment | 50 |
| Start date | 2022-10-05 |
| Completion | 2027-08 |
Conditions
- Thoracic Outlet Syndrome
Interventions
- Ropivacaine
Primary outcomes
- Change in pain level — Time of discharge (approximately 1 day), day 1 post-op, day 3 post-op, day 7 post-op, and day 14 post-op
Measured using the pain visual analog scale (VAS). The VAS line will be 100 mm long with each end marked with "no pain" on the left, and "worst possible pain" on the right; participant identify their pain level by indicating a point on the line between each end and this point is measured from the "No pain" end, and the number of millimeters is reported as the pain score.
Countries
United States