Trials / Enrolling By Invitation
Enrolling By InvitationNCT05544721
A Study of Paravertebral Block in Thoracic Outlet Syndrome
Pre-Operative and Post-Operative Paravertebral Block on Patients With Thoracic Outlet Syndrome.
- Status
- Enrolling By Invitation
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- Sponsor
- Mayo Clinic · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ropivacaine | 0.5% 3-4 mL per level, with levels T1 and T2 will be used as the block injectate |
Timeline
- Start date
- 2022-10-05
- Primary completion
- 2027-08-01
- Completion
- 2027-08-01
- First posted
- 2022-09-16
- Last updated
- 2025-11-14
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT05544721. Inclusion in this directory is not an endorsement.