UnknownNot Applicable

Prospective SPINE Registry

United States5,000 participantsStarted 2020-01-28

Plain-language summary

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.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

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

Exclusion criteria

✕. Patient who is, or is expected to be inaccessible for follow-up.
✕. Patient meets any exclusion criteria required by local law (e.g. age, mental capacity, etc.).
✕. 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.

What they're measuring

Intervention Rates

Timeframe: 1 month, 3 months, 6 months, 12 months, and 24 months

Trial details

NCT IDNCT04176562

SponsorXtant Medical

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2025-03

Contact for this trial

Isabella M Rosales, BS

406-924-5884 irosales@xtantmedical.com

View on ClinicalTrials.gov More Sacroiliac; Fusion trials