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Combination of Fluoroscopy and Ultrasonography Guidance in Sacroiliac Joint Injections

Sacroiliac Joint Pain Clinical Trial

Official title:
Combination of Fluoroscopy and Ultrasonography Guidance in Sacroiliac Joint Injections: Effect on Procedure Time and Radiation Exposure

Clinical Trial Summary

The primary purpose of this study is to investigate the effect of the application of sacroiliac joint injection guided by combination of ultrasonography and fluoroscopy on the duration of the procedure and the amount of radiation exposed during the procedure, compared to the application of only fluoroscopy-guided technique. Secondary objectives are to evaluate the effectiveness of the treatment with both methods and to record the adverse events that may be encountered during the procedure.

Clinical Trial Description

The study was designed as prospective, randomized, controlled trial. The patients who meet the eligibility requirements will be randomized into two groups in a 1:1 ratio to fluoroscopy and ultrasound+fluoroscopy. Processing time will be recorded during injection. "Fluoroscopy time" (sec) and "kerma-area product" (μGy) automatically measured by the fluoroscopy device will be used to evaluate the radiation exposure. Pre-procedural visual analogue scale (VAS) scores and Oswestry Disability Index (ODI) values were noted all the patients. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05944861
Study type Interventional
Source Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
Contact Serdar KESIKBURUN, MD
Phone +903122911402
Email serdarkb@gmail.com
Status Recruiting
Phase N/A
Start date April 15, 2023
Completion date November 15, 2023
View Details
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