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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

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.