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Sacroiliac Joint Disruption
Clinical trial pipeline · Data from ClinicalTrials.gov
See which Sacroiliac Joint Disruption trials you may qualify forClinical trial pipeline · Data from ClinicalTrials.gov
See which Sacroiliac Joint Disruption trials you may qualify forThe purpose of this study is to evaluate outcomes in patients treated with iFuse INTRA Ti for chronic SI joint pain.
The purpose of this study is to evaluate outcomes in patients treated with iFuse TORQ TNT for pelvic fragility fractures.
SALLY studies sacroiliac joint fusion with the iFuse-3D implant.
The purpose of this study is to compare outcomes of subjects undergoing multilevel lumbar fusion (MLF) surgery with and without the iFuse 3-D implants in the "b…
The purpose of this study is to evaluate the outcomes of patients with sacroiliac joint pain treated with the CATAMARAN SI Joint Fusion System.
The objective of this study is to evaluate 6-to-12-month radiographic outcomes of patients with sacroiliac joint disruptions or degenerative sacroiliitis that h…
The purpose of the trial is to confirm the validity and reliability of diagnostic SI joint blocks.
The purpose of this study is to evaluate the long term safety and effectiveness of SI joint fusion using the iFuse Implant System in patients with degenerative…
The purpose of this study is to compare outcomes when patients with degenerative sacroiliitis (arthritis of the SI joint) and or sacroiliac disruption (abnormal…
The purpose of this study is to evaluate the use of the iFuse Implant System to treat degenerative sacroiliitis (arthritis of the SI joint) and sacroiliac disru…