Ultrasound Guided Epidural Block in Axial SPA

• Status: Completed
• Trial end date: 2020-02-12
• Target enrollment: 0
• Participant gender: All

Summary

Study Design: A randomized, prospective, pilot, controlled trial. Setting: Rheumatology and rehabilitation department Minia University and Sohag University Objectives: To evaluate the effectiveness of caudal epidural injections with triamcinolone and lidocaine in managing limited spine mobility in axial SPA.

Methods: Patients were randomly assigned to one of 2 groups, Group I patients received caudal epidural injections with 1% lidocaine hydrochloride (xylocaine AstraZeneca) 9 mL mixed with 1 mL of triamcinolone 40 milligrams (Kenacort Bristol Myers Squip), whereas Group II patients did not receive. Both groups were age and sex matched and both were under treatment with anti TNF and NSAIDs with or without sDMARDs.

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Sohag University
• Treatments: Lidocaine

Criteria

Inclusion Criteria:

• all participants fulfilled the ASAS criteria for axial SPA

• all participants under treatment including bDMARDS and sDMARDs beside NSAIDs

Exclusion Criteria:

• Naive patients not under treatment

• limitation of spine flexion due to non inflammatory causes