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NOT YET RECRUITING
NCT07530497
Real World Evidence of SI-BONE's iFuse TORQ TNT Advancing Treatment of Pelvic Ring Fractures
Sponsor: SI-BONE, Inc.
View on ClinicalTrials.gov
Summary
The purpose of this study is to evaluate outcomes in patients treated with iFuse TORQ TNT for pelvic fragility fractures.
Key Details
Gender
All
Age Range
60 Years - Any
Study Type
OBSERVATIONAL
Enrollment
120
Start Date
2026-08
Completion Date
2028-08
Last Updated
2026-04-15
Healthy Volunteers
No
Conditions
Interventions
DEVICE
iFuse TORQ TNT Implant System
FDA-clear implant used for fracture fixation of the pelvis, including acute, non-acute, and non-traumatic fractures and sacroiliac joint fusion for sacroiliac joint dysfunction including sacroiliac joint disruption and degenerative sacroiliitis.