drugset / Trial / NCT04143165

Ultrasound Guided Epidural Block in Axial SPA

NCT04143165

Phase 4 Completed 52 enrolled Sohag University
RandomizedSingle-groupSingle-blindTreatment

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.

Timeline

Start
2019-10-12
Primary completion
2020-01-12
Completion
2020-02-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Lidocaine Other / unclassified 9 ml Other
Comparator Triamcinolone Other / unclassified 40 mg Other