Prospective SPINE Registry

Xtant Medical

Status: Enrolling

Conditions: Fusion of Joint; Sacroiliac; Fusion; Fusion of Spine; Joint Diseases; Spinal Disease; Spinal Instability; Musculoskeletal Diseases; Spinal Fusion; Spinal Stenosis; Spine; Sacroiliac

Treatments: Device: RTI Spine products

Study type: Observational

Funder types: Industry

Identifiers

NCT04176562

19094

Details and patient eligibility

About

This study is a prospective, multi-center, open label registry designed to collect real-world data on performance and safety data on RTI's spine products.

Enrollment: 5,000 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Candidate for RTI spine product.
2. Willing and able to consent to the study.

Exclusion criteria

1. Patient who is, or is expected to be inaccessible for follow-up.
2. Patient meets any exclusion criteria required by local law (e.g. age, mental capacity, etc.).
3. Other concurrent medical or other condition (chronic or acute in nature) that in the opinion of the investigator may prevent participation or otherwise render patient ineligible for the study.