Find trials
Search tips

Thoracic Outlet Syndrome Pre-Operative and Post-Operative Paravertebral Block

Overview

About this study

The purpose of this study is to assess the patient’s quality of life following the paravertebral block(s) day post-op, 3-day post-op, 7-day post-op, and 2 weeks post-op. Also, to assess the patient’s function following the paravertebral block(s) 1-day post-op, 3-day post-op, 7-day post-op, and 2 weeks post-op, and assess the patient’s pain level following the paravertebral block(s) day post-op, 3-day post-op, 7-day post-op, and 2 weeks post-op.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • All Thoracic Outlet Syndrome patients above the age of 18 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.

  • Eligibility last updated 6/23/12. Questions regarding updates should be directed to the study team contact.

     

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Jacksonville, Fla.

Mayo Clinic principal investigator

Houssam Farres, M.D.

Open for enrollment

Contact information:

Mauricia Buchanan R.N.

Buchanan.Mauricia@mayo.edu

More information

Publications

Publications are currently not available

More about research at Mayo Clinic

.
CLS-20538646

Mayo Clinic Footer