By InvitationPhase 4

A Study of Paravertebral Block in Thoracic Outlet Syndrome

United States50 participantsStarted 2022-10-05

Plain-language 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.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: \- All Thoracic Outlet Syndrome patients scheduled for first rib resection surgery. Exclusion Criteria: * Patients who are pregnant. * Patients with prior first rib resection on side of presentation. * Patients with complex regional pain syndrome (CRPS). * Patients with brachial plexus disorder. * Patients with cervical rib.

What they're measuring

Change in pain level

Timeframe: Time of discharge (approximately 1 day), day 1 post-op, day 3 post-op, day 7 post-op, and day 14 post-op

Trial details

NCT IDNCT05544721

SponsorMayo Clinic

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2027-08

View on ClinicalTrials.gov More Thoracic Outlet Syndrome trials