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Clinical Trial Summary

To study improvements or lack thereof with the interlaminar epidural patients with or without steroids experiences mid back, upper back or neck pain with or without chest wall and upper extremity pain of at least 6-months duration non-responsive to conservative management.


Clinical Trial Description

This is a Single-center, prospective, controlled, double-blind, randomized study in thoracic and cervical regions.

Patients are studied in 2 groups in each region.

- Group I-local anesthetic only.

- Group II-local anesthetic with 6 mg of non-particulate Celestone.

All patients will be unblinded at 12 or 24 months. Non-responsive patients will be unblinded after 3 months and will be crossed over to a different group, if patient consents. Non-responsive patients may be unblinded and withdrawn from the study at any time. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01071369
Study type Interventional
Source Pain Management Center of Paducah
Contact
Status Completed
Phase Phase 4
Start date February 2008
Completion date June 2012

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