Sacroiliitis Clinical Trial
Official title:
The Clinic Application of CBCT XperGuide in Interventional Sacroiliac Joint Pain Therapy
The Research question: Among two standard image guidance techniques [2-dimension (2-D) conventional Fluoroscopy Versus 3-dimension (3-D) Cone-Beam Computed Tomography (CBCT)], which is the better guidance for Sacroiliac Joint Injection therapy and should be used first? The specific aims: To detect the difference of the first-time success rate, the cross-over rate, the procedural time, the radiation exposure, the incidence of adverse events/complications, and overall satisfaction score between the 2-D Fluoroscopy versus 3-D CBCT guidance for SIJ injection.
There are no published research studies comparing the injection success rates, procedure duration, radiation exposure, and patient comfort between the two standard imaging systems. The investigators hypothesize that the newer 3-D Cone-beam Based Computer Tomography (CBCT) image system will result in higher success rates, shorter procedure times, fewer image snapshots during the procedure, and less patient discomfort than conventional 2-D fluoroscopy imaging. Although the radiation exposure from one-time low-dose 3-D CT reconstruction with CBCT image system at the beginning of the procedure is higher, the number of later snapshots with the 3-D system is likely to be significantly lower. Therefore the 3-D system may result in overall equivalent radiation exposure to the 2-D system. A statistical power analysis was conducted and determined that a sample size of 100 (50 per group) will give 80% power for detecting a difference if the true rates are 65% (2-D Fluoroscopy guidance) and 90% (3-D CBCT guidance). For this study, patients undergoing SIJ injection will be randomized to either Fluoroscopy guidance or CBCT guidance. The primary outcome measure is injection success within 3 attempts of needle placement. Statistical analysis will use the Chi-square test to test whether the rate of injection success differs between the two methods of guidance. In order to provide appropriate clinical care, whenever success is not achieved with the initial guidance method then injection using the other guidance method will be attempted. However, the analysis will only consider whether or not injection success was achieved with the initial guidance method to which the subject was randomized. Whether or not injection success was achieved after crossing over to the other guidance method is not relevant to the primary analysis. In summary, the investigators would like to formally analyze the differences in these two standard image guidance options in SIJ injection therapy. The investigators propose to randomly select the first imaging system that will be utilized during standard medical care in patients scheduled to undergo an SIJ injection. Presumed that there is a difference in success rate between these two standard images, the imaging procedures are considered to be a part of the research. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT03689881 -
Value of Tomosynthesis for the Detection of Sacro-iliitis (TOMOS SI)
|
N/A | |
Recruiting |
NCT05396495 -
Safety and Feasibility of the NeurolyserXR for Sacroiliac Joint Pain
|
N/A | |
Completed |
NCT02425631 -
CT Follow-Up of the SImmetry Sacroiliac Joint Fusion System
|
N/A | |
Completed |
NCT02420041 -
Comparing the Effects of Ultrasound Versus Fluoroscopy for Sacroiliac Joint Injections
|
N/A | |
Enrolling by invitation |
NCT05916092 -
Post-Market Clinical Study on a Modular SI Joint Fusion System
|
||
Completed |
NCT04314609 -
Success Rate of Ultrasound Guided Sacroiliac Joint Injection in Sacroiliitis
|
N/A | |
Not yet recruiting |
NCT06034808 -
Frequency of Sacroiliitis in Inflammatory Bowel Disease Patients Using MRI
|
||
Not yet recruiting |
NCT06053255 -
Use of the Neurolyser XR for the Treatment of Low Back Pain Related to Sacroiliitis
|
N/A | |
Completed |
NCT03122119 -
Effectiveness of Ultrasound Guided Platelet Rich Plasma Injections in the Sacroiliac Joint
|
Phase 4 | |
Enrolling by invitation |
NCT05203926 -
Significance and Outcome of Magnetic Resonance Enterography Revealing Sacroiliitis in Crohn's Disease: A Pilot Study
|
N/A | |
Recruiting |
NCT05715463 -
Rheumatology-based Adaptive Intervention for Social Determinants and Health Equity
|
N/A | |
Completed |
NCT02098694 -
Physiotherapy-led Outpatient Clinic for Patients With Spondyloarthritis
|
N/A | |
Recruiting |
NCT05276024 -
Evaluation of the iFuse Bedrock Technique in Association With Posterior Lumbosacral Fusion With Iliac Fixation.
|
||
Completed |
NCT01673633 -
Sacroiliitis in Systemic Sclerosis
|
N/A | |
Enrolling by invitation |
NCT05712850 -
Clinical Outcome and Fusion Results Using the SiJoin® Transfixing Sacroiliac Fusion Device
|
||
Active, not recruiting |
NCT03631030 -
Cooled RF Lesion MRI Characteristics
|
N/A | |
Completed |
NCT03834480 -
Intraartecular Platelet Rich Plasma for Sacroiliitis
|
N/A |