Prospective SPINE Registry

Description

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.

Conditions

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

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Study Overview

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Study Details

Study overview

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.

Prospective Study on Safety and Performance of Surgalign spINE Products

Prospective SPINE Registry

Condition
Sacroiliac; Fusion
Intervention / Treatment

-

Contacts and Locations

Hartford

Hartford Hospital, Hartford, Connecticut, United States, 06102

Boca Raton

Florida Back Institute, Boca Raton, Florida, United States, 33496

Delray Beach

Spine Institute of South Florida, Delray Beach, Florida, United States, 33484

Bartlett

Suburban Orthopaedics, Bartlett, Illinois, United States, 60103

Carmel

Indiana Spine Group, Carmel, Indiana, United States, 46032

Crown Point

DK Orthopedics, Crown Point, Indiana, United States, 46307

Cincinnati

Lindner Center for Research & Education at The Christ Hospit, Cincinnati, Ohio, United States, 45219

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

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

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Xtant Medical,

Study Record Dates

2025-06