Innovative Spinopelvic Solutions With Real-World Evidence
Running, not enrolling
Conditions studied: Sacroiliac Joint Dysfunction, Sacroiliac Joint Pain
In brief
INSPIRE is a prospective decentralized study evaluating post-operative health outcomes in patients who undergo a procedure using implants manufactured by SI-BONE.
Key facts
- Study ID
- NCT06706908
- Run by
- SI-BONE, Inc.
- People needed
- 1000
- Starts
- 2024-12-15
- Expected to finish
- 2034-12-01
- Last updated by the study team
- 2026-04-24
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age > 21 at time of screening.
- Patient will undergo a procedure utilizing an iFuse Implant family product.
- Patient is comfortable communicating in written and spoken English.
- Patient is willing and able to complete study questionnaires online, using either a smartphone, tablet, or computer.
- Patient is willing and able to provide informed consent to participate
You may not qualify if…
- Patient has fibromyalgia.
- Patient has a pain pump.
- Patient is currently receiving or seeking worker's compensation, disability remuneration, and/or involved in injury litigation
Where it is running
- SI-BONE — Santa Clara, California, United States
Full record on ClinicalTrials.gov
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