Clin2
NCT07530497Likely a fitRecruiting

Real-world study of iFuse TORQ TNT for pelvic fractures

Fracture; PelvicInsufficiency FracturesFragility FractureSacroiliac; FusionSacroiliac Joint DisruptionSacroiliac Joint Dysfunction

Part of Injuries & trauma clinical trials.

This study follows patients age 60+ who receive a specific type of pelvic fracture surgery using the iFuse TORQ TNT device. Researchers collect real-world data on how well this treatment works and how patients recover over 12 months.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
120 people
Ages
60 years and older
Study type
Observational

Who can take part

  • Age 60 or older at the time of screening
  • Pelvic fracture confirmed by X-ray and CT scan that matches your pain location
  • Fracture occurred within 6 weeks of a fall/injury, or is an insufficiency fracture limiting your ability to walk
  • Scheduled to have pelvic fixation surgery using the iFuse TORQ TNT device
  • Able to walk/ambulate before your fracture happened
  • Able to complete study visits and surveys for 12 months, or have someone help you do so

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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