Lumbar & Sacroiliac Fusion Study Involving Previously Implanted Devices
This study is a multi-center, observational, prospective and retrospective data collection study
| Condition(s) | Fusion of Spine, Sacroiliac; Fusion |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | This study is a multi-center, observational, prospective and retrospective data collection study |
| Who can participate | Inclusion Criteria: 1. Be 18 years of age or older at the time of enrollment 2. Be willing and able to provide informed consent and comply with study visit requirements 3. Subjects who received a Spinal Simplicity fusion implant(s) (Minuteman G5, Liberty, and/or Patriot) between April 1, 2022 and March 31, 2025 Exclusion Criteria: 1. Unable to provide consent and complete prospective data collection 2. Women who are pregnant, or may become pregnant, during the course of the study 3. Contraindication to CT scanning, in the opinion of the investigator |
| Ages | 18 Years |
| Sex | All |
| Lead sponsor | Spinal Simplicity LLC |
| Locations | Overland Park, Kansas, United States; Overland Park, Kansas, United States; Edina, Minnesota, United States |
| Start date | 2025-09-11 |
| NCT ID | NCT07204288 |
| Official listing | https://clinicaltrials.gov/study/NCT07204288 |